The gene for colour blindness is located on

  • A
    Homologous part of $X$-chromosome
  • B
    Non-homologous part of $X$-chromosome
  • C
    Homologous part of $Y$-chromosome
  • D
    Non-homologous part of $Y$-chromosome

Explore More

Similar Questions

$A$ woman is a carrier for hemophilia (having one gene on each $X$ chromosome) and also carries one gene for color blindness on one $X$ chromosome. She marries a normal man. What will be the phenotype of their offspring?

Write a short note on Haemophilia.

The 'Thala test' is performed for the confirmation of:

The amino acid substituted in sickle cell anaemia is

Give scientific reasons: The product of phenylalanine catabolism excreted in the urine in phenylketonuria.

Vedclass Products

For Students

Vedclass Test Series

Mock tests in real JEE/NEET style with performance analysis. 5-day free trial.

Start Free Trial
For Teachers

Exam Paper Generator

Generate Set A/B/C/D exam papers from 7.5L+ questions in 2 minutes. 3 chapters free.

Try Free
For Institutes

Online Exam Module

Live online exams with unlimited students, 360° analytics & white-label branding.

See Demo