SVOP Polyclonal Antibody, 50ul Dialysis An inactivating nonsense mutation localized

An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9

which suggests its role in PI(3) kinase-mediated signaling events

Experiments with knockout mice indicate that this gene attenuates

Alternative splicing results in four transcript variants encoding the same protein

APEX1 encodes the major AP endonuclease in human cells

SVOP Polyclonal Antibody, 50ul Dialysis An inactivating nonsense mutation localizedSVOP (SV2 Related Protein) is a Protein Coding gene. GO annotations related to this gene include transmembrane transporter activity and ion transmembrane transporter activity. An important paralog of this gene is SV2C.