# Calcium voltage-gated channel subunit alpha1 F

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21102124](https://www.wikidata.org/wiki/Q21102124)  
**Source**: https://4ort.xyz/entity/calcium-voltage-gated-channel-subunit-alpha1-f-q21102124


## References

1. UniProt
2. IUPHAR/BPS Guide to PHARMACOLOGY
3. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/O60840)
4. Q20641742
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60840)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=O60840&geneProductId=UniProtKB:O60840)
7. [Characterization of C-terminal Splice Variants of Cav1.4 Ca2+ Channels in Human Retina](http://www.ebi.ac.uk/QuickGO/annotations?protein=O60840&geneProductId=UniProtKB:O60840)
8. [A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.](http://www.ebi.ac.uk/QuickGO/annotations?protein=O60840&geneProductId=UniProtKB:O60840)
9. [Characterization of C-terminal Splice Variants of Cav1.4 Ca2+ Channels in Human Retina](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60840)
10. [A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60840)
11. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60840)
12. [The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60840)
13. [Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60840)
14. [X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60840)
15. [An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O60840)
16. Ensembl Release 99
17. Transporter Classification database