Septin 2 Polyclonal Antibody, 100ul Serum Defects in this gene may

Defects in this gene may be a cause of partial epilepsy with pericentral spikes (PEPS)| but that has not been proven definitively

MIM 603616) that is required for endocytic membrane fusion| and it serves as a specific guanine nucleotide exchange factor (GEF) for RAB5 (RAB5A

The encoded protein may play a role in the control of craniofacial patterning and the differentiation and survival of inhibitory neurons in the forebrain

This family member is a retinal cone/brain exchanger that can mediate a light-induced decrease in free Ca2+ concentration

Septin 2 Polyclonal Antibody, 100ul Serum Defects in this gene maySEPT2 (Septin 2) is a Protein Coding gene. Diseases associated with SEPT2 include gastrointestinal anthrax and acute orbital inflammation. Among its related pathways are Bacterial invasion of epithelial cells and ERK Signaling. GO annotations related to this gene include GTP binding and enzyme regulator activity. An important paralog of this gene is SEPT6.