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MIRAGE
calcium voltage-gated channel subunit alpha1 S

Summary
Gene Symbol
  • CACNA1S
Organism
Homo sapiens (human)
NCBI Gene
779
KEGG Gene ID
PubChem
779
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Calcium channel
  • Calmodulin-binding
  • Cell membrane
  • Disease variant
  • Disulfide bond
  • Glycoprotein
  • Metal-binding
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Transmembrane helix
  • Voltage-gated channel
Proteins
Displaying all 2 entries
UniProt Protein Name
Q13698
  • Calcium channel, L type, alpha-1 polypeptide, isoform 3, skeletal muscle
  • Voltage-gated calcium channel subunit alpha Cav1.1
B1ALM3
Annotation information from UniProt.
Gene Ontology (GO)
Displaying entries 1 - 5 of 20 in total
GO Term Evidence Code PMID
skeletal system development
extraocular skeletal muscle development
monoatomic ion transport
ion transport
calcium ion transport
GO Hierarchy
Displaying entries 1 - 5 of 12 in total
GO Term Evidence Code PMID
ion channel activity
monoatomic ion channel activity
voltage-gated calcium channel activity
voltage-gated calcium channel activity
voltage-gated calcium channel activity
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
OrthoDB (Group)
Group level
Eukaryota
Group Name
voltage-dependent calcium channel
Functional Category
  • E: Amino acid transport and metabolism
  • P: Inorganic ion transport and metabolism
  • T: Signal transduction mechanisms
Displaying all 7 entries
Gene Ontology
calcium channel activity
calcium ion transmembrane transport
calcium ion transport
high voltage-gated calcium channel activity
metal ion binding
monoatomic ion channel activity
monoatomic ion transport
Displaying all 6 entries
InterPro
Ion transport domain
Voltage-dependent L-type calcium channel, IQ-associated domain
Voltage-dependent calcium channel, L-type, alpha-1 subunit
Voltage-dependent calcium channel, alpha-1 subunit, IQ domain
Voltage-dependent calcium channel, alpha-1 subunit
Voltage-dependent channel domain superfamily
Disease
Disease Ontology
Displaying all 3 entries
DO ID Disease Name Source
DOID:14452 hypokalemic periodic paralysis
DOID:0081350 congenital myopathy 18
DOID:8545 malignant hyperthermia
Ortholog
Displaying all 6 entries
Species Gene ID Alliance of Genome Resources
12292 MGI:88294
682930 RGD:70983
34950 FB:FBgn0001991
570683 ZFIN:ZDB-GENE-090514-1
405791 ZFIN:ZDB-GENE-051227-1
100381134 Xenbase:XB-GENE-5823879
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 6, 2026