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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + TP53  RefSeq IDs +
Approved Name + tumor protein p53 NM_000546 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:11998 Accession Numbers +
Status + Approved AF307851 GenBank  EMBL DDBJ UCSC
Chromosome + 17p13.1 Mouse Genome Database ID +
Previous Symbols +   MGI:98834 MGD ID 
Previous Names +   Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + p53, LFS1 RGD:3889 RGD ID 
Name Aliases + "Li-Fraumeni syndrome" Entrez Gene ID +
Locus Type + gene with protein product 7157 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS11118.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Ensembl Gene ID +
ENSG00000141510 Ensembl GeneView  UCSC 
Pubmed IDs +
6396087, 3456488, 2047879 PMID  CiteXplore 
Specialist Database Links VEGA IDs +
COSMIC Orphanet:120204
 
OTTHUMG00000142618 VEGA GeneView 
OMIM ID (mapped data supplied by NCBI) +
Locus Specific Database Links 191170 OMIM 
IARC TP53 Mutation Database,
p53 Mutation in Human Cancer,
Database of Germline p53 Mutations,
UMD Locus Specific Databases
 
UCSC ID (mapped data supplied by UCSC) +
uc002gij.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
  Q9NP68 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.