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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + SCN5A  RefSeq IDs +
Approved Name + sodium channel, voltage-gated, type V, alpha subunit NM_198056 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:10593 Accession Numbers +
Status + Approved AJ310893 GenBank  EMBL DDBJ UCSC
Chromosome + 3p21 Mouse Genome Database ID +
Previous Symbols + CMD1E MGI:98251 MGD ID 
Previous Names + "sodium channel, voltage-gated, type V, alpha (long QT syndrome 3)" Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + Nav1.5, LQT3, HB1, HBBD, PFHB1, IVF, HB2, HH1, SSS1, CDCD2, CMPD2, ICCD RGD:3637 RGD ID 
Name Aliases + "long QT syndrome 3" Entrez Gene ID +
Locus Type + gene with protein product 6331 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS46796.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Pubmed IDs +
7842012, 15466643, 16382098 PMID  CiteXplore 
VEGA IDs +
OTTHUMG00000156166 VEGA GeneView 
Specialist Database Links Ensembl ID (mapped data supplied by Ensembl) +
IUPHAR:Nav1.5 Orphanet:15254
 
ENSG00000183873 Ensembl GeneView  UCSC 
OMIM ID (mapped data supplied by NCBI) +
Locus Specific Database Links 600163 OMIM 
Long QT Syndrome mutation database,
Gene Connection for the Heart,
Zhejiang University Center for Genetic and Genomic Medicine
 
UCSC ID (mapped data supplied by UCSC) +
uc011ayr.1 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
  Q8IZC9 UniProt  UCSC 

See Column definitions for descriptions of the various data fields. Also see our custom downloads page for bulk access to our data

 


The work of the HGNC is supported by NHGRI grant P41 HG003345, the UK Medical Research Council and the Wellcome Trust.