GPR173 Polyclonal Antibody, 20ul[BT-AP03719] Biomatrix Mutations in this gene cause

Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma

ITIH1 encodes a member of the inter-alpha-trypsin inhibitor family of proteins

CCDC102B may play a role in the pathogenesis of diaphragmatic hernia

Cathepsin Crequires chloride ions for activity and can degrade glucagon

GO annotations related to this gene include metallocarboxypeptidase activity

GPR173 Polyclonal Antibody, 20ul[BT-AP03719] Biomatrix Mutations in this gene causeGPR173 (G protein coupled receptor 173) encodes a member of the G protein coupled receptor 1 family. This protein contains 7 transmembrane domains and conserved cysteine residues.