EMR3 Polyclonal Antibody, 100ul Hybridoma Antibody Sequencing Mutations in this gene are

Mutations in this gene are associated with Wolfram syndrome

GO annotations related to this gene include calcium ion binding and thiol-dependent ubiquitin-specific protease activity

This gene encodes a large abundant protein of striated muscle

Mutations in this gene may contribute to the congenital central hypoventilation syndrome (CCHS) phenotype in rare cases

EMR3 Polyclonal Antibody, 100ul Hybridoma Antibody Sequencing Mutations in this gene areADGRE3 (adhesion G protein coupled receptor E3) encodes a member of the class B seven span transmembrane (TM7) receptor family expressed predominantly by cells of the immune system. Family members are characterized by an extended extracellular region with a variable number of N terminal epidermal growth factor (EGF) like domains coupled to a TM7 domain via a mucin like spacer domain. ADGRE3 is closely linked to the gene encoding egf like molecule