OLR1 Polyclonal Antibody, 100ul Immune Cell Analysis Mutations in this gene cause

Mutations in this gene cause the rare autosomal-recessive systemic autoimmune disease termed autoimmune polyendocrinopathy with candidiasis and ectodermal dystrophy (APECED)

This protein comprises an extracellular domain| an hydrophobic stretch corresponding to a single pass transmembrane region| and an intracellular kinase domain

this protein is essential for the regulation of precursor cell proliferation and the control of neuronal differentiation and migration during hippocampal development

Dematin actin binding protein encoded by DMTN is an actin binding and bundling protein that plays a structural role in erythrocytes

C2orf40 (Chromosome 2 Open Reading Frame 40) is a Protein Coding gene

OLR1 Polyclonal Antibody, 100ul Immune Cell Analysis Mutations in this gene causeThis gene encodes a low density lipoprotein receptor that belongs to the C type lectin superfamily. This gene is regulated through the cyclic AMP signaling pathway. The encoded protein binds, internalizes and degrades oxidized low density lipoprotein. This protein may be involved in the regulation of Fas induced apoptosis. This protein may play a role as a scavenger receptor. Mutations of this gene have been associated with atherosclerosis, risk of