albinism, oculocutaneous Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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Genes

6 genes associated with the disease albinism, oculocutaneous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
OCA2 oculocutaneous albinism II
SLC24A5 solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
SLC45A2 solute carrier family 45, member 2
TYR tyrosinase
TYRP1 tyrosinase-related protein 1