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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + ATM  RefSeq IDs +
Approved Name + ataxia telangiectasia mutated NM_000051 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:795 Accession Numbers +
Status + Approved AB209133 GenBank  EMBL DDBJ UCSC
Chromosome + 11q22-q23 Mouse Genome Database ID (mapped data supplied by MGI) +
Previous Symbols + ATA, ATDC, ATC, ATD MGI:107202 MGD ID 
Previous Names + "ataxia telangiectasia mutated (includes complementation groups A, C and D)" Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + TEL1, TELO1 RGD:1593265 RGD ID 
Name Aliases + "TEL1, telomere maintenance 1, homolog (S. cerevisiae)" Entrez Gene ID +
Locus Type + gene with protein product 472 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS31669.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Ensembl ID (mapped data supplied by Ensembl) +
ENSG00000149311 Ensembl GeneView  UCSC 
OMIM ID (mapped data supplied by NCBI) +
607585 OMIM 
Specialist Database Links UCSC ID (mapped data supplied by UCSC) +
COSMIC Orphanet:15962
 
uc001pkb.1 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
Locus Specific Database Links Q13315 UniProt  UCSC 
Ataxia Telangiectasia Mutated (ATM),
LOVD - Leiden Open Variation Database
 
 

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.