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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + AICDA  RefSeq IDs +
Approved Name + activation-induced cytidine deaminase NM_020661 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:13203 Accession Numbers +
Status + Approved AB040430 GenBank  EMBL DDBJ UCSC
Chromosome + 12p13 Mouse Genome Database ID +
Previous Symbols +   MGI:1342279 MGD ID 
Previous Names +   Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + HIGM2, CDA2, ARP2, AID RGD:1303222 RGD ID 
Name Aliases +   Entrez Gene ID +
Locus Type + gene with protein product 57379 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS41747.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Ensembl ID (mapped data supplied by Ensembl) +
ENSG00000111732 Ensembl GeneView  UCSC 
OMIM ID (mapped data supplied by NCBI) +
605257 OMIM 
Specialist Database Links UCSC ID (mapped data supplied by UCSC) +
COSMIC Orphanet:15479
 
uc001qur.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
Locus Specific Database Links Q9GZX7 UniProt  UCSC 
AICDA base: Mutation registry for Aid deficiency   

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.