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

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

Parkinson's disease

an autosomic dominant congenital malformation

PTM:Ubiquitinated when tyrosine phosphorylated and in a complex with GRB2

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

EMR3 Polyclonal Antibody, 100ul Hybridoma Antibody Sequencing Mutations in this gene mayADGRE3 (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