LPAR4 Polyclonal Antibody, 50ul Hepatocytes Synthesis of the encoded protein

Synthesis of the encoded protein is inhibited by transforming growth factor beta-1

Mutations in this gene are associated with the X-linked lysosomal storage disease mucopolysaccharidosis type II| also known as Hunter syndrome

The protein encoded by this gene| in combination with autophagy protein 12| functions as an E1-like activating enzyme in a ubiquitin-like conjugating system

This gene is a homolog of the Drosophila glial cells missing gene

This gene lies in close proximity to

LPAR4 Polyclonal Antibody, 50ul Hepatocytes Synthesis of the encoded proteinThis gene encodes a member of the lysophosphatidic acid receptor family. It may also be related to the P2Y receptors, a family of receptors that bind purine and pyrimidine nucleotides and are coupled to G proteins. The encoded protein may play a role in monocytic differentiation.