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Gene for colour blindness is located on​
  • a)
    13th chromosome
  • b)
    Y chromosome
  • c)
    21st chromosome
  • d)
    X chromosome
Correct answer is option 'D'. Can you explain this answer?
Most Upvoted Answer
Gene for colour blindness is located on​a)13thchromosomeb)Y chro...
The faulty ‘gene’ for colour blindness is found only on the X chromosome. So, for a male to be colour blind the faulty colour blindness ‘gene’ only has to appear on his X chromosome. For a female to be colour blind it must be present on both of her X chromosomes.
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Gene for colour blindness is located on​a)13thchromosomeb)Y chro...
Introduction:
Color blindness is a genetic disorder that impairs a person's ability to perceive certain colors, usually red and green. It is caused by a genetic mutation that affects the cones in the retina of the eye, which are responsible for color vision. This mutation is located on the X chromosome.

Explanation:
1. Genetic Basis of Color Blindness:
Color blindness is an X-linked recessive genetic disorder. This means that the gene responsible for color blindness is located on the X chromosome. The X chromosome is one of the two sex chromosomes, with females having two X chromosomes (XX) and males having one X and one Y chromosome (XY). Since the gene for color blindness is located on the X chromosome, it primarily affects males.

2. X Chromosome and Inheritance:
The X chromosome carries many genes that are responsible for various traits and characteristics. In males, the Y chromosome does not have a corresponding allele for the genes on the X chromosome. Therefore, if a male inherits a mutated gene on the X chromosome, he will express the trait associated with that gene, as there is no second copy of the gene to mask its effects.

3. Inheritance Pattern of Color Blindness:
When a female carries a mutated gene on one of her X chromosomes, she is considered a carrier. As carriers have a normal copy of the gene on their other X chromosome, they do not exhibit color blindness themselves but can pass the mutated gene to their offspring. If a carrier female has a son, there is a 50% chance that he will inherit the mutated gene and be color blind.

4. Higher Prevalence in Males:
Since males have only one X chromosome, they are more susceptible to color blindness. If a male inherits the mutated gene on his X chromosome, he will be color blind. On the other hand, females need to inherit the mutated gene on both of their X chromosomes to be color blind. This is why color blindness is more commonly seen in males.

Conclusion:
The gene for color blindness is located on the X chromosome. This genetic disorder primarily affects males due to the inheritance pattern of the X chromosome. Understanding the genetic basis of color blindness helps in diagnosing and managing the condition effectively.
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