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Home»NEET Question Answers»Genetic Cross: Color Blind Male and Carrier Female (NEET Biology)
NEET Question Answers

Genetic Cross: Color Blind Male and Carrier Female (NEET Biology)

By November 5, 2024Updated:November 5, 2024No Comments2 Mins Read
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A colour blind male (XcY) marries a carrier female (XCXc). Possible genotype of daughters will be______?

a. XcXc only

b. XCXC only

c. XCXC and XcXc

d. XCXc and XcXc

Hint: Color blindness is defined as the inability to perceive colors correctly. It is an X-linked or sex-linked recessive disorder, meaning that the disease manifests when both alleles are recessive (homozygous recessive alleles) on the X chromosome in the same cell. This condition is commonly referred to as a congenital color vision deficiency.

Complete answer: According to Mendel’s laws of inheritance, specifically the law of segregation and the law of independent assortment, allele combinations occur as follows: if a color-blind male (XcY) mates with a heterozygous female carrier (XCXc), then the possible alleles of the offspring will be: Xc, Y, XC, Xc

The potential combinations are: XcXC, XcXc, YXC, YXc

From these combinations, the daughter genotypes can be: XcXC and XcXc

Therefore, there is a 50% chance that the daughter will be color blind, as the genotype required for color blindness is XcXc. An XCXc daughter will be a carrier of the condition; she can pass on the trait but will not be affected by it herself. The probability ratio for the daughter to inherit the disease is 2:1.

Thus, the correct answer is option (D).

Note:

Color blindness is a condition where a person’s ability to distinguish between colors is reduced. Complete color blindness is known as achromatopsia. The Ishihara color test is a common diagnostic tool for detecting color vision deficiency, which affects about 1 in 12 men and 1 in 200 women.

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