GPR19 Polyclonal Antibody, 50ul Supplements This gene encodes a heavily

This gene encodes a heavily glycosylated protein which is a ligand for the NKG2D type II receptor

disease:Defects in CDKN2A are a cause of Li-Fraumeni syndrome (LFS)

which is essential for G1/S and G2/M phase transitions of eukaryotic cell cycle

Ras homolog

Low expression of the antigen results in impaired immune response

GPR19 Polyclonal Antibody, 50ul Supplements This gene encodes a heavilyGPR19 is a gene on chromosome 12p13. 1 that encodes an orphan G protein coupled receptor. G Protein Coupled Receptor 19 is a orphan receptor. Among its related pathways are Peptide ligand binding receptors. Gene Ontology (GO) annotations related to this gene include G protein coupled receptor activity. An important paralog of this gene is AVPR1B.