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CACNA1F

DescriptionVoltage-dependent L-type calcium channel subunit alpha-1F

Gene and Protein Information

Gene ID778
Uniprot Accession IDs A6NI29 F5CIQ9 O43901 O95226 Q9UHB1
Ensembl ID ENSP00000365441
Symbol CACNAF1 JM8 OA2 AIED COD3 COD4 JMC8 CORDX CSNB2 CORDX3 CSNB2A CSNBX2 Cav1.4 Cav1.4alpha1
FamilyBelongs to the calcium channel alpha-1 subunit (TC 1.A.1.11) family. CACNA1F subfamily.
Sequence
MSESEGGKDTTPEPSPANGAGPGPEWGLCPGPPAVEGESSGASGLGTPKRRNQHSKHKTVAVASAQRSPRALFCLTLANPLRRSCISIVEWKPFDILILLTIFANCVALGVYIPFPEDDSNTANHNLEQVEYVFLVIFTVETVLKIVAYGLVLHPSAYIRNGWNLLDFIIVVVGLFSVLLEQGPGRPGDAPHTGGKPGGFDVKALRAFRVLRPLRLVSGVPSLHIVLNSIMKALVPLLHIALLVLFVIIIYAIIGLELFLGRMHKTCYFLGSDMEAEEDPSPCASSGSGRACTLNQTECRGRWPGPNGGITNFDNFFFAMLTVFQCVTMEGWTDVLYWMQDAMGYELPWVYFVSLVIFGSFFVLNLVLGVLSGEFSKEREKAKARGDFQKQREKQQMEEDLRGYLDWITQAEELDMEDPSADDNLGSMAEEGRAGHRPQLAELTNRRRGRLRWFSHSTRSTHSTSSHASLPASDTGSMTETQGDEDEEEGALASCTRCLNKIMKTRVCRRLRRANRVLRARCRRAVKSNACYWAVLLLVFLNTLTIASEHHGQPVWLTQIQEYANKVLLCLFTVEMLLKLYGLGPSAYVSSFFNRFDCFVVCGGILETTLVEVGAMQPLGISVLRCVRLLRIFKVTRHWASLSNLVASLLNSMKSIASLLLLLFLFIIIFSLLGMQLFGGKFNFDQTHTKRSTFDTFPQALLTVFQILTGEDWNVVMYDGIMAYGGPFFPGMLVCIYFIILFICGNYILLNVFLAIAVDNLASGDAGTAKDKGGEKSNEKDLPQENEGLVPGVEKEEEEGARREGADMEEEEEEEEEEEEEEEEEGAGGVELLQEVVPKEKVVPIPEGSAFFCLSQTNPLRKGCHTLIHHHVFTNLILVFIILSSVSLAAEDPIRAHSFRNHILGYFDYAFTSIFTVEILLKMTVFGAFLHRGSFCRSWFNMLDLLVVSVSLISFGIHSSAISVVKILRVLRVLRPLRAINRAKGLKHVVQCVFVAIRTIGNIMIVTTLLQFMFACIGVQLFKGKFYTCTDEAKHTPQECKGSFLVYPDGDVSRPLVRERLWVNSDFNFDNVLSAMMALFTVSTFEGWPALLYKAIDAYAEDHGPIYNYRVEISVFFIVYIIIIAFFMMNIFVGFVIITFRAQGEQEYQNCELDKNQRQCVEYALKAQPLRRYIPKNPHQYRVWATVNSAAFEYLMFLLILLNTVALAMQHYEQTAPFNYAMDILNMVFTGLFTIEMVLKIIAFKPKHYFTDAWNTFDALIVVGSIVDIAVTEVNNGGHLGESSEDSSRISITFFRLFRVMRLVKLLSKGEGIRTLLWTFIKSFQALPYVALLIAMIFFIYAVIGMQMFGKVALQDGTQINRNNNFQTFPQAVLLLFRCATGEAWQEIMLASLPGNRCDPESDFGPGEEFTCGSNFAIAYFISFFMLCAFLIINLFVAVIMDNFDYLTRDWSILGPHHLDEFKRIWSEYDPGAKGRIKHLDVVALLRRIQPPLGFGKLCPHRVACKRLVAMNMPLNSDGTVTFNATLFALVRTSLKIKTEGNLEQANQELRIVIKKIWKRMKQKLLDEVIPPPDEEEVTVGKFYATFLIQDYFRKFRRRKEKGLLGNDAAPSTSSALQAGLRSLQDLGPEMRQALTCDTEEEEEEGQEGVEEEDEKDLETNKATMVSQPSARRGSGISVSLPVGDRLPDSLSFGPSDDDRGTPTSSQPSVPQAGSNTHRRGSGALIFTIPEEGNSQPKGTKGQNKQDEDEEVPDRLSYLDEQAGTPPCSVLLPPHRAQRYMDGHLVPRRRLLPPTPAGRKPSFTIQCLQRQGSCEDLPIPGTYHRGRNSGPNRAQGSWATPPQRGRLLYAPLLLVEEGAAGEGYLGRSSGPLRTFTCLHVPGTHSDPSHGKRGSADSLVEAVLISEGLGLFARDPRFVALAKQEIADACRLTLDEMDNAASDLLAQGTSSLYSDEESILSRFDEEDLGDEMACVHAL
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Homologous gene and protein info.
SpeciesGene IDGene SymbolNameTax IDOther Gene IDSources
Mouse54652Cacna1fcalcium channel, voltage-dependent, alpha 1F subunit10090MGI:1859639Inparanoid, OMA
Rat114493Cacna1fcalcium voltage-gated channel subunit alpha1 F10116RGD:621535Inparanoid, OMA
Dog480915CACNA1Fcalcium voltage-gated channel subunit alpha1 F9615VGNC:38636Inparanoid, OMA
Horse100062861CACNA1Fcalcium voltage-gated channel subunit alpha1 F9796VGNC:15985Inparanoid, OMA
Cow509779CACNA1Fcalcium voltage-gated channel subunit alpha1 F9913VGNC:26676Inparanoid, OMA

Protein Classes

DTO Classes
protein    /    Ion channel    /    Calcium channel alpha-1 subunit family    /    CACNA1F subfamily    /    Voltage-dependent L-type calcium channel subunit alpha-1F

Associated Approved Drugs

    Associated Active Ligands

      Bibliography

      1.Naylor, M J MJ, Rancourt, D E DE and Bech-Hansen, N T NT. 2000-06-15 Isolation and characterization of a calcium channel gene, Cacna1f, the murine orthologue of the gene for incomplete X-linked congenital stationary night blindness. [PMID:10873387]
      2.Boycott, K M KM, Pearce, W G WG and Bech-Hansen, N T NT. 2000-06 Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F. [PMID:10900517]
      3.Boycott, K M KM and 9 more authors. 2001-02 A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants. [PMID:11281458]
      4.Nakamura, M M, Ito, S S, Terasaki, H H and Miyake, Y Y. 2001-06 Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness. [PMID:11381068]
      5.Wutz, Krisztina K and 11 more authors. 2002-08 Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina. [PMID:12111638]
      6. and Weleber, Richard G RG. 2002-06 Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture). [PMID:12187427]
      7.Zito, Ilaria I and 13 more authors. 2003-02 Mutations in the CACNA1F and NYX genes in British CSNBX families. [PMID:12552565]
      8.Jacobi, Felix Karl FK and 7 more authors. 2003-05 A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness. [PMID:12719097]
      9.Jalkanen, R R and 8 more authors. 2003-06 A new genetic locus for X linked progressive cone-rod dystrophy. [PMID:12807962]
      10.Koschak, Alexandra A and 6 more authors. 2003-07-09 Cav1.4alpha1 subunits can form slowly inactivating dihydropyridine-sensitive L-type Ca2+ channels lacking Ca2+-dependent inactivation. [PMID:12853422]