EP15R Polyclonal Antibody, 100ul Miscellaneous Defects in this gene are

Defects in this gene are a cause of premature ovarian failure 9 (POF9)

Members of this family are zinc-containing type II integral-membrane proteins that are important regulators of neuropeptide and peptide hormone activity

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This gene encodes an enzyme that oxidizes methionine residues on actin| thereby promoting depolymerization of actin filaments

EP15R Polyclonal Antibody, 100ul Miscellaneous Defects in this gene areSeems to be a constitutive component of clathrin coated pits that is required for receptor mediated endocytosis.,PTM: Phosphorylated on tyrosine residues by EGFR.,Contains 1 EF hand domain.,Contains 3 EH domains.,subcellular location: Localized to plasma membrane coated pits.,subunit: Interacts with EPS15, AGFG1 HRB and AGFG2 HRBL. Associates with the clathrin associated adapter protein complex 2 (AP 2).,