It's the X-chromosome, so whichever number corresponds to it.
recessive
X' = color blindnessX'X'-- X --X'Yis a cross that could lead to a color blind female as the mother is homozygous recessive and the father's X chromosome is the recessive color blind trait.
A male with red-green color blindness has the genotype X^cY, where X^c represents the X chromosome carrying the recessive allele for color blindness. He inherited the recessive allele from his mother, who must have at least one X chromosome with the color blindness allele (either X^cX or X^cY). Since males inherit their X chromosome from their mothers and their Y chromosome from their fathers, the mother's genotype determines whether the son will express the condition.
Overall, colorblindness is much more common in males than females due to the fact that it is a sex-linked trait. The gene for colorblindness is carried on the X chromosome. Since this is a recessive condition, males will be more likely to express it due to the fact they only have one X chromosome while the females have two.
Yes, red-green color blindness is typically an X-linked recessive disorder. This means that the gene responsible for red-green color blindness is located on the X chromosome, and individuals who inherit an abnormal gene on their X chromosome are more likely to express the trait if they are male, as they have only one X chromosome.
No - the colour blindness gene is only found on the X chromosome.
recessive
(Apex Learning) She has at least one recessive color blindness allele.
WHAT
X' = color blindnessX'X'-- X --X'Yis a cross that could lead to a color blind female as the mother is homozygous recessive and the father's X chromosome is the recessive color blind trait.
It is found on the non homologous part of the X chromosome.
A male with red-green color blindness has the genotype X^cY, where X^c represents the X chromosome carrying the recessive allele for color blindness. He inherited the recessive allele from his mother, who must have at least one X chromosome with the color blindness allele (either X^cX or X^cY). Since males inherit their X chromosome from their mothers and their Y chromosome from their fathers, the mother's genotype determines whether the son will express the condition.
Plato Users: A and B.
The majority of affected individuals are males. Females are carriers, but are not normally affected. This indicates that the X chromosome is one of the locations for color blindness.
Overall, colorblindness is much more common in males than females due to the fact that it is a sex-linked trait. The gene for colorblindness is carried on the X chromosome. Since this is a recessive condition, males will be more likely to express it due to the fact they only have one X chromosome while the females have two.
Yes, red-green color blindness is typically an X-linked recessive disorder. This means that the gene responsible for red-green color blindness is located on the X chromosome, and individuals who inherit an abnormal gene on their X chromosome are more likely to express the trait if they are male, as they have only one X chromosome.
Color blindness is primarily an inherited genetic condition, passed down through specific genes on the X chromosome. It is more common in males because they have only one X chromosome, meaning if the gene is present on that chromosome, they will exhibit color blindness. Females are less likely to be color blind because they have two X chromosomes, so they would need to inherit the gene from both parents to be affected.