GPR62 Polyclonal Antibody, 50ul Custom DNA Oligos Mutations in this gene result

Mutations in this gene result in Crigler-Najjar syndromes types I and II and in Gilbert syndrome

and is a subunit of mitochondrial ribonuclease P

G-protein coupled receptor for 5-hydroxytryptamine (serotonin)

|disease:Defects in CHEK2 are associated with Li-Fraumeni syndrome 2 (LFS2)

This protein was detected in the insoluble fraction of the affected brain region from Huntington disease patients but not in those from normal controls| which implicated the role in neurodegenerative diseases

GPR62 Polyclonal Antibody, 50ul Custom DNA Oligos Mutations in this gene resultGPR62 is a gene on chromosome 3p21. 2 that encodes Probable G protein coupled receptor 62. G proteincoupled receptors (GPCRs, or GPRs) contain 7 transmembrane domains and transduce extracellular signals through heterotrimeric G proteins. Among its related pathways are GPCRs. Gene Ontology (GO) annotations related to this gene include G protein coupled receptor activity. An important paralog of this gene is GPR61.