SH3G3 Polyclonal Antibody, 20ul PCR Series Defects in this gene are

Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome

RPL14 contains a trinucleotide (GCT) repeat tract whose length is highly polymorphic

The subunit encoded by this gene is subject to RNA editing at multiple sites within the first and second transmembrane domains

mediating the recruitment of RNA polymerase I to rDNA promoter regions

Expression of this gene is induced by the tumor suppressor p53 and in response to DNA damage

SH3G3 Polyclonal Antibody, 20ul PCR Series Defects in this gene areAn N terminal amphipathic helix, the BAR domain and a second amphipathic helix inserted into helix 1 of the BAR domain (N BAR domain) induce membrane curvature and bind curved membranes.,Implicated in endocytosis. May recruit other proteins to membranes with high curvature.,Belongs to the endophilin family.,Contains 1 BAR domain.,Contains 1 SH3 domain.,subcellular location: Associated with postsynaptic endosomes in hippocampal neurons. Associated with