Entrez gene ID | | 114493 |
Official gene symbol | | Cacna1f |
Full name | | calcium channel, voltage-dependent, L type, alpha 1F subunit |
Aliases | | - |
Gene summary | | mutation of the human homolog causes incomplete X-linked congentital stationary night blindness (CSNB2) [RGD] |
Location | | Chromosome: 0 Locus: Xq13 |
Gene position | | 26908849 - 26937164 Map Viewer |
Gene orientation | | minus |
Gene size | | 28316 bp |
Gene sequence |
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