Both X chromosomes must carry the recessive trait. Since males only have one X chromosome, it is much easier for males to have the recessive phenotype. Put another way, a female would have to receive an X chromosome with the recessive gene from both parents, which would mean the father already displays the recessive disorder.
color blindness is one
a male with one recessive allele
males have only one X chromosomes
Recessive gene of X chromosome. more common in men as they have only one x chromosome but in female there are 2 X chromosome. If one of X chromosome in female has this recessive gene, they become a carrier. If both the X chromosome in female has this gene, they show baldness
It is very much recessive with only one exception, which is that there is a large portion of women who simply carry the trait but dont actually have it. If you are to procreate with a female carrier than your chances of having a hemophiliac child are still not very high. You can find all the info you need by using a Punnett Square method to figure out the chances of hemophiliac children with 2 parents.
Usually female.
Haemophilia is a sex-linked recessive disorder - which means it can skip a generation, but only if it is carried in the female line.A female can be a carrier of haemophilia, but a male cannot. This is because males only have one X chromosome, so if they have a defective X they will have the disorder. If a father has haemophilia, all of his daughters will also have haemophilia.
The mother has a 50% chance of passing the defective recessive gene to her daughters who will be carries of the disorder (like their mother).
Hemophilia is a recessive allele condition. Men can get hemophilia alot easier than women as the allele is found on the XY Chomosome pair. With men. they do not have the extra "tail" on the Y chromosome compared to the XX with a female. If the person has the recessive allele on the X chromosome and this person is male, they will be a hemophiliac as they do not have a 'pair' allele which could be dominant to stop the condition expressing itself. On a female, if there is a recessive (hemophilia) allele on one of the X chromosomes but on the other is a Dominant (normal) allele then she will be a carrier of the faulty gene but will not suffer from the condition herself. If the female have a recessive (faulty) gene on each of the XX chromosomes, then she will be a sufferer of the disease.
Anyone can be a carrier of a recessive genetic disorder (as long as it is not associated with the sex chromosomes) no matter what their gender since "carrier" refers to an individual that is heterozygous for the recessive allele and therefore phenotypically normal. Specifically, sexlinked genetic disorders can be "carried" by a heterozygous female but males (having only one X chromosome) cannot. Males will either be free of the defective gene or be affected.
color blindness is one
If the female is recessive for both traits, she would carry two copies of the recessive gene for each trait. Therefore, the eggs from this female would all carry two copies of the recessive gene for each trait.
wheat disorder female
The female would have to have the blood genotype of AO. The recessive O is masked by the female with the domaint A allele. Their offsprings genotype would be BO the B would be from the father and the recessive O from the mother.
While the condition affects the males, it is CARRIED by the females, who do not suffer the effects of hemophilia, and can pass the disorder to THEIR female offspring.
a male with one recessive allele
The population of the United States of America are mostly affected by Binge Eating Disorder.