FOH1B Polyclonal Antibody, 20ul Cryopreservation Mutations in this gene have

Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP)

there are multiple processed pseudogenes of RPS20 dispersed through the genome

These proteins are secreted ligands of leucine-rich repeat containing G protein-coupled receptors that enhance Wnt signaling through the inhibition of ubiquitin E3 ligases

The gene encoding FAM84B maps to human chromosome 8

Members of this family encode 7-transmembrane domain proteins that are receptors for the Wingless type MMTV integration site family of signaling proteins

FOH1B Polyclonal Antibody, 20ul Cryopreservation Mutations in this gene haveFOLH1B (Folate Hydrolase 1B) is a Protein Coding gene. Among its related pathways are Metabolism and Amino acid synthesis and interconversion (transamination). Has both folate hydrolase and N acetylated alpha linked acidic dipeptidase (NAALADase) activity. Exhibits a dipeptidyl peptidase IV type activity.