Chromosome 9.
Chromosome 9.
*affected
yes it is. It affects chromosome 11.
Ocular albinism (OA1) is caused by a genetic defect on chromosome 11 of the GPR143 gene. Oculocutaneous albinism type 2 (OCA2 or P gene albinism) results from a genetic defect on chromosome 15 in the P protein that helps the tyrosinase enzyme to function. Oculocutaneous albinism type 3 (OCA3) is rarely described and results from a genetic defect on chromosome 9 in TYRP1, a protein related to tyrosinase. Oculocutaneous albinism type 4 (OCA4) results from a genetic defect in chromosome 5 at position 13.3, in the SLC45A2 protein that helps the tyrosinase enzyme to function.
An Autosomal recessive pattern is one in which certain genes of the X sex chromosome are turned off, autosomal is in reference to the X chromosome and the fact that the genes are turned off is indicated by the recessive. So in the case of Albinism the pigmentation genes in the X chromosome are turned off causing the various side effects.
no albinism is a genetic disorders that changes an offsprings physical appearance from its original parents. it may also bring out the offsprings recessive traits. its also a cause of mental retardation
When a gene is linked to a chromosome, it means that the gene is physically located on that chromosome. This means that the gene is inherited along with the chromosome it is located on, and may be inherited together with other nearby genes on the same chromosome.
No, not all sex-linked traits are located on the X chromosome. Some sex-linked traits can also be located on the Y chromosome.
It's located on the X chromosome.
Yes, linked genes are genes located on the same chromosome.
The gene that causes cystic fibrosis is located on chromosome 7, which is an autosome, not a sex chromosome.
chromosome 7 according to the internet