KLOT Polyclonal Antibody, 20ul Metabolic enzymes Mutations in this gene are

Mutations in this gene are associated with the autosomal recessive disorder congenital disorder of glycosylation| type IIk

This action is an important step in detoxification of these compounds

It is active on peptide linkages involving the carboxyl group of lysine or arginine

GLP1R encodes a 7-transmembrane protein that functions as a receptor for glucagon-like peptide 1 (GLP-1) hormone

also named as TEM3 and TEM7

KLOT Polyclonal Antibody, 20ul Metabolic enzymes Mutations in this gene areThis gene encodes a type I membrane protein that is related to beta glucosidases. Reduced production of this protein has been observed in patients with chronic renal failure (CRF), and this may be one of the factors underlying the degenerative processes (e. g., arteriosclerosis, osteoporosis, and skin atrophy) seen in CRF. Also, mutations within this protein have been associated with ageing and bone loss.