Lentiviral human RAB3GAP2 sgRNA gene knockout kit

Human RAB3GAP2

Gene symbol: RAB3GAP2
Synonyms: p150 RAB3-GAP150 RAB3GAP150 SPG69 WARBM2
Species: HUMAN
Gene ID: 25782
Summary: The protein encoded by this gene belongs to the RAB3 protein family, members of which are involved in regulated exocytosis of neurotransmitters and hormones. This protein forms the Rab3 GTPase-activating complex with RAB3GAP1, where it constitutes the regulatory subunit, whereas the latter functions as the catalytic subunit. This gene has the highest level of expression in the brain, consistent with it having a key role in neurodevelopment. Mutations in this gene are associated with Martsolf syndrome.[provided by RefSeq, Oct 2009].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_012414:14:14