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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + GLRA1  Mouse Genome Database ID (mapped data supplied by MGI) +
Approved Name + glycine receptor, alpha 1 MGI:95747 MGD ID 
HGNC ID + HGNC:4326 Rat Genome Database ID (mapped data supplied by RGD) +
Status + Approved RGD:2704 RGD ID 
Chromosome + 5q31-q33 CCDS IDs +
Previous Symbols + STHE CCDS4320.1 CCDS ID 
Previous Names + "glycine receptor, alpha 1 (startle disease/hyperekplexia)" Pubmed IDs +
Aliases +   1355335, 8298642 PMID  CiteXplore 
Name Aliases + "startle disease/hyperekplexia", "stiff person syndrome" VEGA IDs +
Locus Type + gene with protein product OTTHUMG00000130121 VEGA GeneView 
  Ensembl ID (mapped data supplied by Ensembl) +
Gene Symbol Links ENSG00000145888 Ensembl GeneView  UCSC 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Entrez Gene ID (mapped data supplied by NCBI) +
2741 Gene  Map Viewer 
RefSeq (mapped data supplied by NCBI) +
NM_000171 GenBank EMBL DDBJ UCSC
Specialist Database Links OMIM ID (mapped data supplied by NCBI) +
IUPHAR:α1 COSMIC Orphanet:16141
 
138491 OMIM 
UCSC ID (mapped data supplied by UCSC) +
Locus Specific Database Links uc003lut.2 UCSC Index 
LOVD - Leiden Open Variation Database  UniProt ID (mapped data supplied by UniProt) +
P23415 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.