CMTA1 Polyclonal Antibody, 100ul Drying & Desiccation Defects in this gene likely

Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss

The SOCS box may act as a bridge between specific substrate-binding domains and E3 ubiquitin protein ligases

Members of the connecdenn family| such as DENND1A| function as guanine nucleotide exchange factors (GEFs) for the early endosomal small GTPase RAB35 (MIM 604199) and bind to clathrin and clathrin adaptor protein-2 (AP2

It also serves as an entry for certain mutant strains of herpes simplex virus and pseudorabies virus

CMTA1 Polyclonal Antibody, 100ul Drying & Desiccation Defects in this gene likelydisease: Defects in CAMTA1 are detected in patients with oligodendroglioma and astrocytoma.,Transcriptional activator. May act as a tumor suppressor.,induction: Detected at low levels at interphase and in resting cells. Up regulated during S phase and mitosis. Levels decrease at the end of mitosis.,Belongs to the CAMTA family.,Contains 1 CG 1 DNA binding domain.,Contains 1 IPT TIG domain.,Contains 3 ANK repeats.,Contains 3 IQ domains.,subunit: May