ANXA8 Rabbit Polyclonal Antibody, 50ul Organelle Studies Pseudogenes of this gene are

Pseudogenes of this gene are located on chromosomes 9

Defects in PRF1 cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2)

The encoded protein contains a zinc finger and is a helicase that appears to be part of the peroxisome proliferator activated receptor alpha interacting complex

The protein encoded by VCP (valosin containing protein) is a member of a family that includes putative ATP-binding proteins involved in vesicle transport and fusion

MRGPRG (MAS Related GPR Family Member G) is a Protein Coding gene

ANXA8 Rabbit Polyclonal Antibody, 50ul Organelle Studies Pseudogenes of this gene areThis gene encodes a member of the annexin family of evolutionarily conserved Ca2+ and phospholipid binding proteins. The encoded protein may function as an an anticoagulant that indirectly inhibits the thromboplastin specific complex. Overexpression of this gene has been associated with acute myelocytic leukemia. A highly similar duplicated copy of this gene is found in close proximity on the long arm of chromosome 10.