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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + ABCD1  RefSeq IDs +
Approved Name + ATP-binding cassette, sub-family D (ALD), member 1 NM_000033 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:61 Accession Numbers +
Status + Approved Z21876 GenBank  EMBL DDBJ UCSC
Chromosome + Xq28 Mouse Genome Database ID +
Previous Symbols + ALD MGI:1349215 MGD ID 
Previous Names +   Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + AMN, ALDP, adrenoleukodystrophy RGD:1562128 RGD ID 
Name Aliases +   Entrez Gene ID +
Locus Type + gene with protein product 215 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS14728.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Pubmed IDs +
8441467, 6795626 PMID  CiteXplore 
VEGA IDs +
OTTHUMG00000024215 VEGA GeneView 
Specialist Database Links Ensembl ID (mapped data supplied by Ensembl) +
COSMIC Orphanet:15058
 
ENSG00000101986 Ensembl GeneView  UCSC 
OMIM ID (mapped data supplied by NCBI) +
Locus Specific Database Links 300371 OMIM 
X-linked Adrenoleukodystrophy Database,
Mental Retardation database
 
UCSC ID (mapped data supplied by UCSC) +
uc004fif.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
  P33897 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.