factor - a factor is a gene. organisms have 2 genes for every trait they show. allele – an allele...
TRANSCRIPT
Factor - A factor is a gene Organisms have 2 genes for every trait they show
Allele ndash An allele is a version or form of a gene (dominant vs recessive)
If an organismrsquos two genes are the same it is homozygous for that trait Ex RR or rr
If your two genes are the different it is heterozygous for that trait Ex Rr
The two alleles you actually have in your DNA is your genotype
Ex RR Rr and rr are possible genotypes
The way your alleles are shown on the outside or expressed is known as your phenotype
Ex rolling or not be able to roll is a phenotype
The Law of Dominance States that some alleles are dominant and some alleles are recessive
A dominant allele will be expressed (show up) in the phenotype if it is present in the genotype
A recessive allele will be expressed only if no dominant allele is present
Mendelrsquos law of segregation states that alleles will separate when gametes (sex cells) are formed and they will go to different sex cells
Mendelrsquos ExperimentshellipcontinuedhellipIndependent Assortment
Mendelrsquos ExperimentshellipcontinuedhellipIndependent Assortment
Mendel wanted to determine if certain traits were passed along together (linked)
Ex Do yellow and round pea traits get passed along together to offspring
Do green and wrinkled traits get passed along together
The experiment Y=Yellow R = Roundy = green r = wrinkled
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1 YR YRyr YyRr YyRr Phenotype
ratioyr YyRr YyRr
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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The two alleles you actually have in your DNA is your genotype
Ex RR Rr and rr are possible genotypes
The way your alleles are shown on the outside or expressed is known as your phenotype
Ex rolling or not be able to roll is a phenotype
The Law of Dominance States that some alleles are dominant and some alleles are recessive
A dominant allele will be expressed (show up) in the phenotype if it is present in the genotype
A recessive allele will be expressed only if no dominant allele is present
Mendelrsquos law of segregation states that alleles will separate when gametes (sex cells) are formed and they will go to different sex cells
Mendelrsquos ExperimentshellipcontinuedhellipIndependent Assortment
Mendelrsquos ExperimentshellipcontinuedhellipIndependent Assortment
Mendel wanted to determine if certain traits were passed along together (linked)
Ex Do yellow and round pea traits get passed along together to offspring
Do green and wrinkled traits get passed along together
The experiment Y=Yellow R = Roundy = green r = wrinkled
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1 YR YRyr YyRr YyRr Phenotype
ratioyr YyRr YyRr
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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-
The Law of Dominance States that some alleles are dominant and some alleles are recessive
A dominant allele will be expressed (show up) in the phenotype if it is present in the genotype
A recessive allele will be expressed only if no dominant allele is present
Mendelrsquos law of segregation states that alleles will separate when gametes (sex cells) are formed and they will go to different sex cells
Mendelrsquos ExperimentshellipcontinuedhellipIndependent Assortment
Mendelrsquos ExperimentshellipcontinuedhellipIndependent Assortment
Mendel wanted to determine if certain traits were passed along together (linked)
Ex Do yellow and round pea traits get passed along together to offspring
Do green and wrinkled traits get passed along together
The experiment Y=Yellow R = Roundy = green r = wrinkled
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1 YR YRyr YyRr YyRr Phenotype
ratioyr YyRr YyRr
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
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-
Mendelrsquos ExperimentshellipcontinuedhellipIndependent Assortment
Mendelrsquos ExperimentshellipcontinuedhellipIndependent Assortment
Mendel wanted to determine if certain traits were passed along together (linked)
Ex Do yellow and round pea traits get passed along together to offspring
Do green and wrinkled traits get passed along together
The experiment Y=Yellow R = Roundy = green r = wrinkled
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1 YR YRyr YyRr YyRr Phenotype
ratioyr YyRr YyRr
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
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Mendelrsquos ExperimentshellipcontinuedhellipIndependent Assortment
Mendel wanted to determine if certain traits were passed along together (linked)
Ex Do yellow and round pea traits get passed along together to offspring
Do green and wrinkled traits get passed along together
The experiment Y=Yellow R = Roundy = green r = wrinkled
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1 YR YRyr YyRr YyRr Phenotype
ratioyr YyRr YyRr
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
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The experiment Y=Yellow R = Roundy = green r = wrinkled
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1 YR YRyr YyRr YyRr Phenotype
ratioyr YyRr YyRr
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
- Slide 8
- Slide 9
- Slide 10
- Slide 11
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- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1 YR YRyr YyRr YyRr Phenotype
ratioyr YyRr YyRr
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
- Slide 8
- Slide 9
- Slide 10
- Slide 11
- Slide 12
- Slide 13
- Slide 14
- Slide 15
- Slide 16
- Slide 17
- Slide 18
- Slide 19
- Slide 20
- Slide 21
- Slide 22
- Slide 23
- Slide 24
- Slide 25
- Slide 26
- Slide 27
- Slide 28
- Slide 29
- Slide 30
- Slide 31
- Slide 32
- Slide 33
- Slide 34
- Slide 35
- Slide 36
- Slide 37
- Slide 38
- Slide 39
- Slide 40
- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1 YR YRyr YyRr YyRr Phenotype
ratioyr YyRr YyRr
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
- Slide 8
- Slide 9
- Slide 10
- Slide 11
- Slide 12
- Slide 13
- Slide 14
- Slide 15
- Slide 16
- Slide 17
- Slide 18
- Slide 19
- Slide 20
- Slide 21
- Slide 22
- Slide 23
- Slide 24
- Slide 25
- Slide 26
- Slide 27
- Slide 28
- Slide 29
- Slide 30
- Slide 31
- Slide 32
- Slide 33
- Slide 34
- Slide 35
- Slide 36
- Slide 37
- Slide 38
- Slide 39
- Slide 40
- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1 YR YRyr YyRr YyRr Phenotype
ratioyr YyRr YyRr
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
- Slide 8
- Slide 9
- Slide 10
- Slide 11
- Slide 12
- Slide 13
- Slide 14
- Slide 15
- Slide 16
- Slide 17
- Slide 18
- Slide 19
- Slide 20
- Slide 21
- Slide 22
- Slide 23
- Slide 24
- Slide 25
- Slide 26
- Slide 27
- Slide 28
- Slide 29
- Slide 30
- Slide 31
- Slide 32
- Slide 33
- Slide 34
- Slide 35
- Slide 36
- Slide 37
- Slide 38
- Slide 39
- Slide 40
- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
The experiment Y=Yellow R = Roundy = green r = wrinkled
Parents true breeding for both traitsYYRR x yyrr
Poss YR YR yr yrGam
F1 YR YRyr YyRr YyRr Phenotype
ratioyr YyRr YyRr
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
- Slide 8
- Slide 9
- Slide 10
- Slide 11
- Slide 12
- Slide 13
- Slide 14
- Slide 15
- Slide 16
- Slide 17
- Slide 18
- Slide 19
- Slide 20
- Slide 21
- Slide 22
- Slide 23
- Slide 24
- Slide 25
- Slide 26
- Slide 27
- Slide 28
- Slide 29
- Slide 30
- Slide 31
- Slide 32
- Slide 33
- Slide 34
- Slide 35
- Slide 36
- Slide 37
- Slide 38
- Slide 39
- Slide 40
- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
Did this tell Mendel whether or not traitsAre passed along together or linked
No
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
- Slide 8
- Slide 9
- Slide 10
- Slide 11
- Slide 12
- Slide 13
- Slide 14
- Slide 15
- Slide 16
- Slide 17
- Slide 18
- Slide 19
- Slide 20
- Slide 21
- Slide 22
- Slide 23
- Slide 24
- Slide 25
- Slide 26
- Slide 27
- Slide 28
- Slide 29
- Slide 30
- Slide 31
- Slide 32
- Slide 33
- Slide 34
- Slide 35
- Slide 36
- Slide 37
- Slide 38
- Slide 39
- Slide 40
- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
Mendel crossed the F1 individualsYyRr x YrRr
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
- Slide 8
- Slide 9
- Slide 10
- Slide 11
- Slide 12
- Slide 13
- Slide 14
- Slide 15
- Slide 16
- Slide 17
- Slide 18
- Slide 19
- Slide 20
- Slide 21
- Slide 22
- Slide 23
- Slide 24
- Slide 25
- Slide 26
- Slide 27
- Slide 28
- Slide 29
- Slide 30
- Slide 31
- Slide 32
- Slide 33
- Slide 34
- Slide 35
- Slide 36
- Slide 37
- Slide 38
- Slide 39
- Slide 40
- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
Mendel crossed the F1 individualsYyRr x YrRr
Poss Gam
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
- Slide 8
- Slide 9
- Slide 10
- Slide 11
- Slide 12
- Slide 13
- Slide 14
- Slide 15
- Slide 16
- Slide 17
- Slide 18
- Slide 19
- Slide 20
- Slide 21
- Slide 22
- Slide 23
- Slide 24
- Slide 25
- Slide 26
- Slide 27
- Slide 28
- Slide 29
- Slide 30
- Slide 31
- Slide 32
- Slide 33
- Slide 34
- Slide 35
- Slide 36
- Slide 37
- Slide 38
- Slide 39
- Slide 40
- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
Mendel crossed the F1 individualsYyRr x YyRr
Poss YR Yr yR yr YR Yr yR yrGam
Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
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Phenotype ratio Period 3 Bio ndash Wait untiltomorrow for Phenotype ratios
Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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Did this tell Mendel wether or not traitsAre passed along together or linked
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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-
Mendel found that traits were NOT linked and alleles assort independent of one another during gamete formation the Law of Independent Assortment
What might be an exception to this law
An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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An exception to this would be when genes are found on the same chromosome
Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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Carnations Incomplete Dominance
Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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Snapdragon Incomplete Dominance
Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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Roan Cattle Codominance (RW)
Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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Sickle cell anemia Codominant
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
- Slide 8
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- Slide 43
- Slide 44
- Slide 45
-
clumps with anti-A anti-B anti-A none
anti-B
Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
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- Slide 2
- Slide 3
- Slide 4
- Slide 5
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Genes Chromosomes and Heredity
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
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-
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
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- Slide 37
- Slide 38
- Slide 39
- Slide 40
- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
Genes Chromosomes and Heredity
In 1902 it was discovered that Mendelrsquos genes were found on chromosomes
Chromosomes can be viewed in their homologous pairs by photographing them and organizing them into a picture known as a karyotype
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
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- Slide 37
- Slide 38
- Slide 39
- Slide 40
- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
A normal human karyotype
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
- Slide 8
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- Slide 38
- Slide 39
- Slide 40
- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
Humans have 46 chromosomes in 23 pairs The fist 22 pairs are called autosomes
The last pair are called sex chromosomes
XX = female (chromosomes are homologous)
XY = male because a Y is present (they are nonhomologous)
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
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- Slide 41
- Slide 42
- Slide 43
- Slide 44
- Slide 45
-
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
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- Slide 45
-
Sex linkage ndash A gene is said to be sex-linked when it is located on the sex chromosomes These are most commonly on the X chromosome
Sex linked traits are more commonly found in males than in females
Why Look at some examples
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
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- Slide 45
-
Hemophilia ndash Normal is dominantNormal genotypeMale Female
Hemophilia genotypeMale Female
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
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- Slide 43
- Slide 44
- Slide 45
-
Fruit fly eye color ndash Red is dominant over whiteRed genotypeMale Female
White genotypeMale Female
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
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- Slide 43
- Slide 44
- Slide 45
-
Draw identical twins here
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
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- Slide 43
- Slide 44
- Slide 45
-
Himalayan rabbit Siamese Cat
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
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- Slide 45
-
The environment can affect the way your genes are expressed This means that the phenotype is affected
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
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- Slide 7
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-
End Result
Different polypeptide or protein chainscan be made from differentamino acid sequences These proteinswill have different functions
Chromosomal Mutations
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
- Slide 7
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- Slide 43
- Slide 44
- Slide 45
-
Diseases associated with chromosomal mutations
- Downs Syndrome- Kleinfelters disease - Turnerrsquos Syndrome
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
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-
MUTATIONS IN THE DNATypes of mutations
1048708Frame Shift - when either insertion or deletion of one or two nucleotide bases When this occurs the ldquoreading framerdquo is changed so that all thecodons read after the mutation are incorrect
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
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-
Disorders that result from DNA mutations
1048708 Sickle Cell Anemia1048708 PKU1048708 Cystic Fibrosis
- Slide 1
- Slide 2
- Slide 3
- Slide 4
- Slide 5
- Slide 6
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