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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + GAA  Enzyme IDs +
Approved Name + glucosidase, alpha; acid 3.2.1.20 3.2.1.20 
HGNC ID + HGNC:4065 Mouse Genome Database ID (mapped data supplied by MGI) +
Status + Approved MGI:95609 MGD ID 
Chromosome + 17q25.2-q25.3 Rat Genome Database ID (mapped data supplied by RGD) +
Previous Symbols +   RGD:735227 RGD ID 
Previous Names +   Entrez Gene ID +
Aliases +   2548 Gene  Map Viewer 
Name Aliases + "Pompe disease", "glycogen storage disease type II" CCDS IDs +
Locus Type + gene with protein product CCDS32760.1 CCDS ID 
  Ensembl ID (mapped data supplied by Ensembl) +
Gene Symbol Links ENSG00000171298 Ensembl GeneView  UCSC 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
RefSeq (mapped data supplied by NCBI) +
NM_000152 GenBank EMBL DDBJ UCSC
OMIM ID (mapped data supplied by NCBI) +
606800 OMIM 
Specialist Database Links UCSC ID (mapped data supplied by UCSC) +
COSMIC Orphanet:16088
 
uc002jxq.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
Locus Specific Database Links P10253 UniProt  UCSC 
GAA - Pompe disease (glycogen storage disease type II),
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.