Question

Albinism is a genetic disorder caused by an autosomal recessive allele. The dominant allele results in...

Albinism is a genetic disorder caused by an autosomal recessive allele. The dominant allele results in the wildtype pigmentation.

a) If an albino marries a homozygous person for the wildtype pigmentation allele, what would be the expected phenotype and genotype of their children?

b) If an albino marries a person with wildtype pigmentation but that carries the albino allele, what would be the expected phenotypes and genotypes of their children?

c) Two parents of wildtype pigmentation had an albino child. How is this possible? Indicate the genotypes of the parents.

0 0
Add a comment Improve this question Transcribed image text
Answer #1

a)Since albinism is caused by recessive allele, let genotype be represented by aa for albino. Genotype for homozygous wild type( without 'a'allele) is AA.

M/F

a

a

A

Aa

Aa

A

Aa

Aa

Expected Genotype is Aa

Expected phenotype is wild type pigmentation(because offspring would carry only one albino allele).

b) A person who carries the albino allele but displays wild type pigmentation, is said to be a carrier with genotype Aa. Albino genotype aa.

M/F

a

a

A

Aa

Aa

a

aa

aa

Expected Genotype is : Aa, aa

Expected phenotype is : wild type pigmentation 50%, albino 50%

c)This is possible if both the parents are carriers. A person who carries the albino allele but displays wild type pigmentation, is said to be a carrier with genotype Aa.

M/F

A

a

A

AA

Aa

a

aa

aa

Expected phenotype is : wild type pigmentation 50%, albino 50%

Add a comment
Know the answer?
Add Answer to:
Albinism is a genetic disorder caused by an autosomal recessive allele. The dominant allele results in...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • albinism is caused by a recessive QUESTION 6 Albinism (lack of skin and hair pigmentation) is...

    albinism is caused by a recessive QUESTION 6 Albinism (lack of skin and hair pigmentation) is caused by a recessive autosomal allele. A woman and man both normally pigmented, have an albino child together. For this trait, what is the genotype of the albino child? O A. It is unknown, because not enough information is provided. O B. heterozygous O C. homozygous dominant OD.homozygous recessive O E. It depends on the environment that the child lives in. QUESTION 7 in...

  • In humans, albinism is caused by a recessive allele (a) while normal pigmentation is caused by...

    In humans, albinism is caused by a recessive allele (a) while normal pigmentation is caused by the dominant allele (A). a) If two pigmented parents have an albino child, what must the genotypes of the parents be? b) What is the probability that if they have another child, that child will be albino? c) What is the probability that the next two children are albinos? d) What is the probability that they have one albino and one pigmented child? Be...

  • Albinism (lack of skin pigmentation) is caused by a recessive mutation on one of the autosomal...

    Albinism (lack of skin pigmentation) is caused by a recessive mutation on one of the autosomal chromosomes. A man and woman, both with normally pigmented skin, have an albino child together. For this trait, what is the genotype of the albino child? homozygous dominant homozygous recessive O heterozygous O hemizygous O unknown, not enough information

  • In humans, normal pigmentation is due to a dominant gene A. Albinism is due to a...

    In humans, normal pigmentation is due to a dominant gene A. Albinism is due to a recessive allele a. A normal man marries an albino woman and their first child is albino. What are the genotypes of all three people? If they have more children what would their pigmentation be like?

  • b. Use the following genetic symbols to answer the questions: Normal pigment allele N Albinism allele-n...

    b. Use the following genetic symbols to answer the questions: Normal pigment allele N Albinism allele-n The genotype of an albino individual is The genotype of a "carrier" is The genotype of a normal individual is Use the solved example as a guide to complete the following albinism problem and predict the occurrence of this disorder in the childrer c. Carrier pareX Albino parent Carrier parent X Carrier parent Possible genotype of the parents Possible genotype of the parents: Nr...

  • Lab Exercise 10 6) Fragile X disorder is a sex linked recessive disorder. Albinism is an...

    Lab Exercise 10 6) Fragile X disorder is a sex linked recessive disorder. Albinism is an autosomal recessive characterized by a lack of pigment in the skin, eyes and hair. HINT: THE GENES INO INVOLVED ARE ON TWO DIFFERENT CHROMOSOMES! Kyra is a carrier for Fragile X disorder and is unaffected by albinism. Kyra's mother has unpigmented skin, eyes and hair. Kyra marries Randy who has albinism, and does not ha Fragile X disorder. a. What is Kyra's genotype? b....

  • 6. The allele for curly hair is codominant to the allele for straight hair, the heterozygote...

    6. The allele for curly hair is codominant to the allele for straight hair, the heterozygote has wavy hair. if two people with wavy hair marry, what hair types would you expect among their offspring 7. Two children in a family have blood type. The mother has type B, and the father has type A a. What are the genotypes of all of the individuals? b. What is the probability that their next child will have blood type O? 8....

  • 6 A human trait that is caused by an autosomal dominant mutant allele has a penetrance...

    6 A human trait that is caused by an autosomal dominant mutant allele has a penetrance of 50%. A man who is heterozygous for this mutant allele marries a woman who is homozygous recessive for the normal allele. If they have two children then what is the probability that both children will show the normal phenotype? O 1/4 o 1/2 03/16 0 7/8 09/16

  • 9. In humans, normal pigmentation is due to a dominant gene (C), albinism to it's recessive...

    9. In humans, normal pigmentation is due to a dominant gene (C), albinism to it's recessive allele (c). A normal pigmented man has children with an albino woman. Their first child is an albino. What are the genotypes of each of these three people? IF THEY HAD MORE CHILDREN, WHAT WOULD BE THE GENOTYPIC AND PHENOTYPIC RATIO PROBABILITIES? EXPLAIN YOU REASONING!! SHOW YOUR WORK USING A PUNNETT SQUARE!! Wor m mentation(c)

  • Albinism (lack of skin pigmentation) is caused by a recessive mutation on one of the autosomal...

    Albinism (lack of skin pigmentation) is caused by a recessive mutation on one of the autosomal chromosomes. A man and woman, both with normally pigmented skin, have an albino child together. The couple decide to have a second child. What is the probability that this second child will also be albino? zero O twenty-five % O fifty % seventy five % o one hundred %

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT