GPR143

G Protein-Coupled Receptor 143

This gene encodes a protein that binds to heterotrimeric G proteins and is targeted to melanosomes in pigment cells. This protein is thought to be involved in intracellular signal transduction mechanisms. Mutations in this gene cause ocular albinism type 1, also referred to as Nettleship-Falls type ocular albinism, a severe visual disorder. A related pseudogene has been identified on chromosome Y. [provided by RefSeq, Dec 2009]

CHROMOSOME X GPR143 Xp22.2 genetics.jdge.cc

SNPs0

These are a select few set of SNPs chosen to research within GPR143 to do with the area Dopamine.

No variant data entered yet.