VCP(Phospho Ser352) Polyclonal Antibody, 100ul Reagent Reservoirs Defects in this gene are

Defects in this gene are the cause of tritan color blindness (tritanopia)

Mutations in this gene have also been associated with various cancers

GO annotations related to this gene include ligand-dependent nuclear receptor transcription coactivator activity and nuclear hormone receptor binding

This gene is a member of the receptors of complement activation (RCA) family and is located in the 'cluster RCA' region of chromosome 1

VCP(Phospho Ser352) Polyclonal Antibody, 100ul Reagent Reservoirs Defects in this gene areThe protein encoded by this gene is a member of a family that includes putative ATP binding proteins involved in vesicle transport and fusion, 26S proteasome function, and assembly of peroxisomes. This protein, as a structural protein, is associated with clathrin, and heat shock protein Hsc70, to form a complex. It has been implicated in a number of cellular events that are regulated during mitosis, including homotypic membrane fusion, spindle pole