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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + ERCC1  RefSeq IDs +
Approved Name + excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence) NM_001983 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:3433 Mouse Genome Database ID +
Status + Approved MGI:95412 MGD ID 
Chromosome + 19q13.32 Rat Genome Database ID (mapped data supplied by RGD) +
Previous Symbols +   RGD:1306992 RGD ID 
Previous Names +   Entrez Gene ID +
Aliases +   2067 Gene  Map Viewer 
Name Aliases +   CCDS IDs +
Locus Type + gene with protein product CCDS12662.1 CCDS ID 
  Pubmed IDs +
Gene Symbol Links 6462228 PMID  CiteXplore 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Ensembl ID (mapped data supplied by Ensembl) +
ENSG00000012061 Ensembl GeneView  UCSC 
OMIM ID (mapped data supplied by NCBI) +
126380 OMIM 
Specialist Database Links UCSC ID (mapped data supplied by UCSC) +
COSMIC Orphanet:139163
 
uc002pbv.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
Locus Specific Database Links P07992 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.