Homo sapiens Protein: SCN7A
Summary
InnateDB Protein IDBP-293775.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SCN7A
Protein Name sodium channel, voltage-gated, type VII, alpha
Synonyms NaG; Nav2.1; Nav2.2; SCN6A;
Species Homo sapiens
Ensembl Protein ENSP00000386796
InnateDB Gene IDBG-74239 (SCN7A)
Protein Structure
UniProt Annotation
Function Mediates the voltage-dependent sodium ion permeability of excitable membranes. Assuming opened or closed conformations in response to the voltage difference across the membrane, the protein forms a sodium-selective channel through which Na(+) ions may pass in accordance with their electrochemical gradient.
Subcellular Localization Membrane; Multi-pass membrane protein.
Disease Associations
Tissue Specificity Heart and uterus.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005216 ion channel activity
GO:0005248 voltage-gated sodium channel activity
GO:0005272 sodium channel activity
GO:0005515 protein binding
Biological Process
GO:0006811 ion transport
GO:0006814 sodium ion transport
GO:0006936 muscle contraction
GO:0019228 neuronal action potential
GO:0034765 regulation of ion transmembrane transport
GO:0035725 sodium ion transmembrane transport
GO:0055078 sodium ion homeostasis
GO:0055085 transmembrane transport
GO:0086010 membrane depolarization during action potential
Cellular Component
GO:0001518 voltage-gated sodium channel complex
GO:0005886 plasma membrane
GO:0016020 membrane
GO:0097386 glial cell projection
Protein Structure and Domains
PDB ID
InterPro IPR001696 Voltage gated sodium channel, alpha subunit
IPR005821 Ion transport domain
IPR010526 Sodium ion transport-associated
PFAM PF00520
PF06512
PRINTS PR00170
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q01118
PhosphoSite PhosphoSite-Q01118
TrEMBL Q16278
UniProt Splice Variant
Entrez Gene 6332
UniGene Hs.635368
RefSeq NP_002967
HUGO HGNC:10594
OMIM 182392
CCDS CCDS46442
HPRD 08355
IMGT
EMBL AC074101 AC092583 M91556 S75992
GenPept AAA59899 AAD14203