| GENE NAME | CACNA1F |
| CHROMOSOME | X |
| ENSEMBL ID | None |
| ENTREZ ID | ENSG00000102001 |
| UNIPROT ACCESSION NUMBER | O60840 |
| GO MOLECULAR FUNCTION | ['voltage-gated calcium channel activity', 'high voltage-gated calcium channel activity', 'metal ion binding'] |
| ESSENTIAL IN MOUSE | Non-essential |
| PATHWAYS | hsa04010; hsa04020; hsa04022; hsa04024; hsa04260; hsa04261; hsa04270; hsa04723; hsa04725; hsa04726; hsa04727; hsa04911; hsa04912; hsa04921; hsa04924; hsa04925; hsa04927; hsa04929; hsa04934; hsa04935; hsa05010; hsa05020; hsa05022; hsa05410; hsa05412; hsa05414; hsa04010; hsa04020; hsa04022; hsa04024; hsa04260; hsa04261; hsa04270; hsa04723; hsa04725; hsa04726; hsa04727; hsa04911; hsa04912; hsa04921; hsa04924; hsa04925; hsa04927; hsa04929; hsa04934; hsa04935; hsa05010; hsa05020; hsa05022; hsa05410; hsa05412; hsa05414 |
| 1 combination linked to CACNA1F | OLI1566 |
| 1 variant linked to CACNA1F | CACNA1F:c.4360C>G, p.Leu1454Val |
| 1 disease linked to CACNA1F | Syndrome with 46,XY disorder of sex development |