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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + ABCA12  RefSeq IDs +
Approved Name + ATP-binding cassette, sub-family A (ABC1), member 12 NM_173076 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:14637 Accession Numbers +
Status + Approved AF418105 GenBank  EMBL DDBJ UCSC
Chromosome + 2q34 Mouse Genome Database ID +
Previous Symbols +   MGI:2676312 MGD ID 
Previous Names +   Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + DKFZP434G232, LI2, ICR2B RGD:1304586 RGD ID 
Name Aliases + "ichthyosis congenita II, lamellar ichthyosis B" Entrez Gene ID +
Locus Type + gene with protein product 26154 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS33372.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Ensembl Gene ID +
ENSG00000144452 Ensembl GeneView  UCSC 
Pubmed IDs +
11435397, 12915478 PMID  CiteXplore 
Specialist Database Links VEGA IDs +
COSMIC Orphanet:15049
 
OTTHUMG00000154801 VEGA GeneView 
OMIM ID (mapped data supplied by NCBI) +
Locus Specific Database Links 607800 OMIM 
  UCSC ID (mapped data supplied by UCSC) +
uc002vew.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
  Q86UK0 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.