Mouse Basigin, BSG ELISA Kit , 96T Polyclonal Antibodies Defects in this protein or

Defects in this protein or in its signalling pathway are a cause of holoprosencephaly (HPE)| a d

Hereditary hemorrhagic telangiectasia

It has been shown to interact with TRAF family members

The NRGN gene contains four exons and three introns

GPR42 appears to have arisen by tandem duplication of FFAR3 and have lost the ability to activate G-protein family in respose to carboxylate ligands primarily due to an amino acid change at position 174

Mouse Basigin, BSG ELISA Kit , 96T Polyclonal Antibodies Defects in this protein or[Isoform 1]: Essential for normal retinal maturation and development (PubMed: 10967074, PubMed: 11273674, PubMed: 11853760). Acts as a retinal cell surface receptor for NXNL1 and plays an important role in NXNL1 mediated survival of retinal cone photoreceptors (PubMed: 25957687). In association with glucose transporter SLC16A1 GLUT1 and NXNL1, promotes retinal cone survival by enhancing aerobic glycolysis and accelerating the entry of glucose into