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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + ACTG1  RefSeq IDs +
Approved Name + actin, gamma 1 NM_001614 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:144 Mouse Genome Database ID (mapped data supplied by MGI) +
Status + Approved MGI:87906 MGD ID 
Chromosome + 17q25 Rat Genome Database ID (mapped data supplied by RGD) +
Previous Symbols + ACTG, DFNA20, DFNA26 RGD:1304556 RGD ID 
Previous Names + "deafness, autosomal dominant 20; deafness, autosomal dominant 26" Entrez Gene ID +
Aliases +   71 Gene  Map Viewer 
Name Aliases +   CCDS IDs +
Locus Type + gene with protein product CCDS11782.1 CCDS ID 
  Ensembl Gene ID +
Gene Symbol Links ENSG00000184009 Ensembl GeneView  UCSC 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Pubmed IDs +
14684684 PMID  CiteXplore 
OMIM ID (mapped data supplied by NCBI) +
102560 OMIM 
Specialist Database Links UCSC ID (mapped data supplied by UCSC) +
COSMIC Orphanet:166815
 
uc002kal.1 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
Locus Specific Database Links P63261 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.