No, my wife is dumb as a post but my kid can do math like you wouldn't believe.
Yes. It is found as a mutation on the X chromosome (a sex chromosome) so it is sex linked. The gene for Fragile X is carried on the X chromosome. Because both males (XY) and females (XX) have at least one X chromosome, both can pass on the mutated gene to their children.
X-linked refers to a gene carried on the X chromosome, one of the two sex chromosomes.
Traits like colorblindness, hemophilia, and Duchenne muscular dystrophy are carried on the X chromosome. These traits are caused by mutations in specific genes located on the X chromosome, such as the OPN1LW and OPN1MW genes for colorblindness and the F8 and F9 genes for hemophilia.
A Y-linked gene is a gene that is carried on the Y chromosome, a sex chromosome found only in male cells. In humans, the most commonly mentioned Y-linked gene encodes a protein called testis-determining factor (TDF). As the name suggests, TDF prompts the development of the testes. Since only genetic males have a Y chromosome, only males express TDF and go on to develop testes. In general, genes carried on the sex chromosomes (X and Y) are considered to be "linked" to that chromosome. Genes carried on the X chromosome are considered X-linked in the same way that TDF is considered Y-linked.
Because hemophilia is a disease linked to a recessive gene on the X-chromosome, females have another X-chromosome to block out the diseased one. However, males have only one X-chromosome, so they are more often subject to hemophilia.
Because the gene that causes hemophilia is located on the X chromosome, so it will occur in males more frequently than in females.
Some genes carried on the X chromosome include those responsible for traits such as color blindness, hemophilia, and Duchenne muscular dystrophy. Inheritance of these genes follows specific patterns due to the X-linked nature of these traits.
It is a gene located on either sex chromosome (X or Y chromosome).
It is a gene located on either sex chromosome (X or Y chromosome).
It is a gene located on either sex chromosome (X or Y chromosome).
Females have two X chromosomes, so if one carries a gene for a sex-linked disorder, the other X chromosome can often compensate for it. This means that females are less likely to express the disorder compared to males who have only one X chromosome.
The Factor X gene is said to be located on the X chromosome. Females have two X chromosomes, whereas males only have one. The other chromosome they have is a Y chromosome.