6 genes annotated in human
An autosomal recessive disease characterized by abnormal pigmentation of the skin, hair and eyes.
In addition to gene-name show these genes:
Click on a gene's description to view its network relationships with genes known to be involved in "oculocutaneous albinism"
|Name||Description||Probability||Func Analog Organism|
|TYRP1||tyrosinase-related protein 1||0.001|
|OCA2||oculocutaneous albinism II||0.001|
|MC1R||melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)||0.001|
|ABCC6||ATP-binding cassette, sub-family C (CFTR/MRP), member 6||0.001|
|SLC45A2||solute carrier family 45, member 2||0.000|
|TYR||tyrosinase (oculocutaneous albinism IA)||0.000|