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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + ABCB7  RefSeq IDs +
Approved Name + ATP-binding cassette, sub-family B (MDR/TAP), member 7 NM_004299 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:48 Accession Numbers +
Status + Approved AF038950 GenBank  EMBL DDBJ UCSC
Chromosome + Xq13.3 Mouse Genome Database ID +
Previous Symbols + ABC7 MGI:109533 MGD ID 
Previous Names +   Entrez Gene ID +
Aliases + EST140535, Atm1p, ASAT 22 Gene  Map Viewer 
Name Aliases +   CCDS IDs +
Locus Type + gene with protein product CCDS14428.1 CCDS ID 
  Pubmed IDs +
Gene Symbol Links 9143506 PMID  CiteXplore 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
VEGA IDs +
OTTHUMG00000021862 VEGA GeneView 
Ensembl ID (mapped data supplied by Ensembl) +
ENSG00000131269 Ensembl GeneView  UCSC 
Specialist Database Links OMIM ID (mapped data supplied by NCBI) +
COSMIC Orphanet:15053
 
300135 OMIM 
UCSC ID (mapped data supplied by UCSC) +
Locus Specific Database Links uc004ebz.2 UCSC Index 
Mental Retardation database  UniProt ID (mapped data supplied by UniProt) +
O75027 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.