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.
The unit of heredity found on a chromosome is called a gene.
nucleus → chromosome → gene
An allele is an alternative form of a gene that is found at the same location on a chromosome.
Thalassemia is carried on chromosome 11 and chromosome 16, depending on the type. The alpha-thalassemia gene is located on chromosome 16, while the beta-thalassemia gene is found on chromosome 11. Mutations in these genes affect the production of hemoglobin, leading to the various forms of thalassemia.
The gene that determines male biological traits is called the SRY gene, which is located on the Y chromosome. This gene plays a crucial role in the development of male sex characteristics during embryonic development.
Obviously.
Chromosome 2
Chromosome 7
if you mean chromosome its the 15th......
Chromosome numbers: 1, 14, 19, and 21 are affected by Alzheimer's disease.
Chromosome 21 is tripled in Down syndrome.
A gene found on a sex chromosome is known as a sex-linked gene. Alleles are the different forms of a gene.
Chromosome number 8. (Gene: RECQL4 gene.)
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.
No - the colour blindness gene is only found on the X chromosome.
The unit of heredity found on a chromosome is called a gene.
yes each gene has 100 chromosome on it