There are several depending on the type. Congenital hypertrichosis lanuginosa may be caused by an inverse mutation on the 8q chromosome. Congenital generalized hypertrichosis has a dominant pattern of inheritance and has been linked to chromosome xq24-q27. Congenital generalized hypertrichosis terminalis is thought to be caused by genetic changes on chromosome 17. The gene MAP2K6 may be a factor contributing to this condition.
Hypertrichosis can have various underlying genetic causes. Specific genes that have been associated with hypertrichosis include the SOX3 gene on the X chromosome and the FOXC2 gene on chromosome 16. However, hypertrichosis can also be a symptom of other genetic or chromosomal abnormalities.
Male genetics are found in the Y chromosome.
The unit of heredity found on a chromosome is called a gene.
nucleus → chromosome → gene
Someone whose parent is a carrier of the gene; because the gene is on the X chromosome which is inherited by your mother it would most likely be from her.
yes it can
Obviously.
Chromosome 2
Chromosome 7
if you mean chromosome its the 15th......
The gene associated with narcolepsy is found on chromosome 12 in humans. This gene is called HLA-DQB1*06:02 and is a key genetic factor contributing to susceptibility to narcolepsy.
Chromosome numbers: 1, 14, 19, and 21 are affected by Alzheimer's disease.
Chromosome 21 is tripled in Down syndrome.
Chromosome number 8. (Gene: RECQL4 gene.)
A gene found on a sex chromosome is known as a sex-linked gene. Alleles are the different forms of a gene.
No - the colour blindness gene is only found on the X chromosome.
Male genetics are found in the Y chromosome.
The unit of heredity found on a chromosome is called a gene.