GPR26 Polyclonal Antibody, 20ul Pathway and Network Analysis Mutations in this gene cause

Mutations in this gene cause ovarian dysgenesis type 1

A pseudogene of this gene is found on chromosome X

It is thought to modulate bone morphogenetic protein (BMP) receptor function by serving as an accessory or coreceptor

and thus regulated by

It is located at the 3' of the NOC4 (neighbor of COX4) gene in a head-to-head orientation

GPR26 Polyclonal Antibody, 20ul Pathway and Network Analysis Mutations in this gene causeThis gene encodes a G protein couple receptor protein. G protein coupled receptors are a large family of membrane proteins that are involved in cellular responses to environmental stimuli, neurotransmitters, and hormones. The encoded protein may play a role in neurodegenerative diseases. Epigenetic silencing of this gene has been observed in gliomas.