GPR39 Polyclonal Antibody, 20ul Centrifugal Filter Mutations in RAB3GAP2 are associated

Mutations in RAB3GAP2 are associated with Martsolf syndrome

macrocephaly

suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls

NFKB1/p50 and RELA

USP36 (ubiquitin specific peptidase 36) encodes a member of the peptidase C19 or ubiquitin-specific protease family of cysteine proteases

GPR39 Polyclonal Antibody, 20ul Centrifugal Filter Mutations in RAB3GAP2 are associatedThis gene is a member of the ghrelin receptor family and encodes a rhodopsin type G protein coupled receptor (GPCR). The encoded protein is involved in zinc dependent signaling in epithelial tissue in intestines, prostate and salivary glands. The protein may also be involved in the pathophysiology of depression.