Question

The inheritance of color blindness in humans is due to a recessive gene located on the...

  1. The inheritance of color blindness in humans is due to a recessive gene located on the X chromosome (X linked). X+ (normal) > Xc (color blind)

a. If a color-blind boy is born to parents both of whom have normal vision, what are the genotypes of the three individuals?

b. What is the probability that the second child born to that couple will be a color-blind daughter?

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

Colorblindness is a condition which is inherited by the X-linked recessive gene present on X-chromosome. Here X+ is normal, dominant and Xc is colorblind, recessive.

Females have two X-linked alleles because females are XX, and male have one X-linked allele that is male are XY. So a male to be colorblind requires only a single Xc gene whereas a female to be colorblind requires two Xc genes, because for the expression of recessive character presence of two recessive alleles are necessary.

Qa) In the question it is given that both the parents are normal and a colorblind boy is born to them.

Answer-The genotype of father XY, mother XcX, boy XcY.

Explanation:-

Here the boy to be colorblind requires a single Xc gene from his mother, because it is a male the presence of a single recessive Xc gene is sufficient to express the recessive character.

Usually boys get the defective Xc gene from their mother, so here the genotype of mother will be XcX (she is a carrier of colorblindness), and genotype of father will be XY (as he is normal), because both the parents are normal, the genotype of the colorblind boy will be XcY.

Qb) Here it is asked the probability of the second child who is a girl born to that couple will be a colorblind.

Answer-

The chance of a girl being colorblind is 0%.

Explanation:-

There is no chance of the second child who is a daughter being colorblind, because a girl to become colorblind got to inherit two defective Xc genes one from father and one from mother, because the gene responsible for colorblndness is a recessive gene and for its expression, in females it requires two recessive genes. But here the father is normal, so daughters cannot be colorblind.

From the below punnette square it can be well studied.

When a women who is a carrier of color-blindness crossed with a male who is normal than the offspring will be

The genotypes of both the parents are female (XcX), male (XY)

When XcX crossed with XY

X

Y

Xc

XcX

(carrier female)

XcY

(colorblind male)

X

XX(normal female)

XY(normal male)

So there is no chance of the second child being born to the couple is a colorblind daughter, because here their sons have 50% chance of being colorblind (XcY) and 50% chance of being normal male (XY) and their daughter have 50% chance of being a carrier (XcX) and 50% chance of being completely normal (XX).

Add a comment
Know the answer?
Add Answer to:
The inheritance of color blindness in humans is due to a recessive gene located on the...
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
  • Red-green color blindness is due to an X-linked recessive allele in humans. A widow�s peak (a...

    Red-green color blindness is due to an X-linked recessive allele in humans. A widow�s peak (a hairline that comes to a peak in the middle of the forehead) is due to an autosomal dominant allele. Consider the following family history: A man with a widow�s peak and normal color vision marries a color-blind woman with a straight hairline. The man�s father had a straight hairline, as did both of the woman�s parents. Use the family history to make predictions about...

  • The following was gathered on color blindness in one family. Color blindness in humans is an...

    The following was gathered on color blindness in one family. Color blindness in humans is an X-linked recessive trait. Indicate the genotypes for individuals 1 and 2 in generation I. Would it ever be possible for individuals 2 and 4 in generation II to have a child with normal vision? Explain why or why not. If individual 8 had a child, what would be the probability of the child having normal vision?                                   Graded Assignment-2 Compatibility Mode] - Word (Product...

  • In this set of questions, you will need to be able to apply inheritance patterns of...

    In this set of questions, you will need to be able to apply inheritance patterns of two different characters/genes. One gene is inherited in a sex-linked pattern, while the other gene is inherited through an autosomal gene. (Answer choices include 0, 0.25, 0.5, 0.75, and 1.) In this set of questions, you will need to be able to apply inheritance patterns of two different characters/genes. One gene is inherited in a sex-linked pattern, while the other gene is inherited through...

  • Suppose color blindness is a X linked trait in humans. It is also recessive. A phenotypically...

    Suppose color blindness is a X linked trait in humans. It is also recessive. A phenotypically normal woman has a father with color blindness. This woman marries a man with normal vision. What is the chance of their children being color blind? What is the chance of their daughters being color blind?

  • 13. Color blindness is a condition in which a person cannot distinguish specific colors from one...

    13. Color blindness is a condition in which a person cannot distinguish specific colors from one another. For example, the person may not be able to distinguish red from green or blue from yellow. However, the person is able to distinguish some colors. Because color blind people are not blind and they can see some colors, many people prefer to use the term color-deficient. In humans, the condition for normal vision dominates color blindness. Both alleles are linked to the...

  • po 1 pour Part 3 - Pedigree Analysis (3 points) In humans, normal color vision vs....

    po 1 pour Part 3 - Pedigree Analysis (3 points) In humans, normal color vision vs. red-green color blindness is conditioned by alleles C (dominant normal) and c (recessive red-green color blind) at a sex-linked locus. A color-blind father and normal vision mother have three children. One daughter has normal vision; another daughter and son have red-green color-blindness. Draw the pedigree chart for this family, using the generally accepted symbols and including a legend, and indicate the genotypes of all...

  • Red-green color blindness is due to an X-linked recessive allele in humans. A widow's peak (a...

    Red-green color blindness is due to an X-linked recessive allele in humans. A widow's peak (a hairline that comes to a peak in the middle of the forehead) is due to an autosomal dominant allele. Consider the following family history: A man with a widow's peak and normal color vision marries a color-blind woman with a straight hairline. The man's father had a straight hairline, as did both of the woman's parents. Use the family history to make predictions about...

  • A healthy woman with a color blind father married an unaffected man, and their first child,...

    A healthy woman with a color blind father married an unaffected man, and their first child, a boy, had hemophilia. Both color blindness and hemophilia are due to x-linked recessive mutations and the relevant genes are separated by 20 cM. This couple plans to have a second child. What is the probability of having: a) a boy with hemophilia (regardless of his vision) b) a color blind girl without hemophilia? c) a child with both hemophilia and color blindness? d)...

  • Red-green color blindness is X-linked recessive. A woman with normal color vision has a father who...

    Red-green color blindness is X-linked recessive. A woman with normal color vision has a father who is colorblind. The woman has a child with a man with normal color vision. What is the probability their child is a boy and is colorblind? A. 1/8 B. 1/4 C. 1/2 D. 3/4 E. 0

  • PROCEDURE: Analysis of a pedigree The most common type of color blindness is red-green Coreessive color...

    PROCEDURE: Analysis of a pedigree The most common type of color blindness is red-green Coreessive color perception defeet. It's due to a blind allele). X-linked red-green have normal vision, but mutation on the X chromosome (i.e. a red-green color color blindness is a recessive trait. Females heterozygous are carriers of the trait. The color perception defect man inherited from both parents (homozygous recessive). Byor blind if the inenedigree c chromosome from their mothers and become red-green color chromosome has the...

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