Name

CACNA1F Gene

calcium channel, voltage-dependent, L type, alpha 1F subunit

This 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 disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Aug 2013]

cacna1f Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cacna1f in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

CACNA1F Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for CACNA1F from the Pathway Commons Protein-Protein Interactions dataset.