CAC1F Polyclonal Antibody, 50ul sgRNA Oligos Multiple alternative transcript variants have

Multiple alternative transcript variants have been described for this gene

CD2AP and ARHGEF7

Arg-19 and Arg-25 are dimethylated

serine and threonine metabolism and Lysine degradation

Mutations in Nkx2-6 are associated with persistent truncus arteriosus

CAC1F Polyclonal Antibody, 50ul sgRNA Oligos Multiple alternative transcript variants haveThis gene encodes a multipass transmembrane protein that functions as an alpha 1 subunit of the voltage dependent calcium channel, which mediates the influx of calcium ions into the cell. The encoded protein forms a complex of alpha 1, alpha 2 delta, beta, and gamma subunits in a 1: 1: 1: 1 ratio. Mutations in this gene can cause X linked eye disorders, including congenital stationary night blindness type 2A, cone rod dystropy, and Aland Island eye