about
P527
P688
A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F geneThe electroretinographic diagnosis of the incomplete form of congenital stationary night blindnessAn L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindnessLoss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindnessCharacterization of C-terminal Splice Variants of Cav1.4 Ca2+ Channels in Human Retina
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Calcium voltage-gated channel subunit alpha1 F
@nl
protèin
@ace
بروتين في الإنسان العاقل
@ar
name
Calcium voltage-gated channel subunit alpha1 F
@en
type
label
Calcium voltage-gated channel subunit alpha1 F
@en
altLabel
CACNA1F
@en
calcium channel, voltage-dependent, L type, alpha 1F subunit
@en
voltage-dependent L-type calcium channel subunit alpha-1F
@en
voltage-gated calcium channel subunit alpha Cav1.4
@en
prefLabel
Calcium voltage-gated channel subunit alpha1 F
@en
P129
P361
P527
P637
P680
P681
P682
P705
P352
P31
P352
P361
P527
P637
NP_001243718
NP_001243719
XP_011542285
XP_016885325
P680
P681
P682
P702
P703
P705
ENSP00000321618
ENSP00000365427
ENSP00000365441
ENSP00000418961
P7260
1.A.1.11.11