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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + ABCA1  RefSeq IDs +
Approved Name + ATP-binding cassette, sub-family A (ABC1), member 1 NM_005502 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:29 Accession Numbers +
Status + Approved AJ012376 GenBank  EMBL DDBJ UCSC
Chromosome + 9q31 Mouse Genome Database ID +
Previous Symbols + ABC1, HDLDT1 MGI:99607 MGD ID 
Previous Names +   Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + TGD RGD:631344 RGD ID 
Name Aliases + "Tangier disease" Entrez Gene ID +
Locus Type + gene with protein product 19 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS6762.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Pubmed IDs +
8088782 PMID  CiteXplore 
VEGA IDs +
OTTHUMG00000020417 VEGA GeneView 
Specialist Database Links Ensembl ID (mapped data supplied by Ensembl) +
COSMIC Orphanet:17351
 
ENSG00000165029 Ensembl GeneView  UCSC 
OMIM ID (mapped data supplied by NCBI) +
Locus Specific Database Links 600046 OMIM 
  UCSC ID (mapped data supplied by UCSC) +
uc004bcl.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
  Q9UN09 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.