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Activation-induced (cytidine) deaminase

AICDA
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases AICDA, AID, ARP2, CDA2, HEL-S-284, HIGM2, activation-induced cytidine deaminase, activation induced cytidine deaminase
External IDs MGI: 1342279 HomoloGene: 7623 GeneCards: AICDA
Gene location (Human)
Chromosome 12 (human)
Chr. Chromosome 12 (human)
Chromosome 12 (human)
Genomic location for AICDA
Genomic location for AICDA
Band 12p13.31 Start 8,602,166 bp
End 8,612,871 bp
RNA expression pattern
PBB GE AICDA 219841 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_020661
NM_001330343

NM_009645

RefSeq (protein)

NP_001317272
NP_065712

NP_033775

Location (UCSC) Chr 12: 8.6 – 8.61 Mb Chr 12: 122.55 – 122.56 Mb
PubMed search

5JJ4

NM_020661
NM_001330343

NM_009645

NP_001317272
NP_065712

NP_033775

Activation-induced cytidine deaminase, also known as AICDA and AID, is a 24 kDa enzyme which in humans is encoded by the AICDA gene. It creates mutations in DNA by deamination of cytosine base, which turns it into uracil (which is recognized as a thymine). In other words, it changes a C:G base pair into a U:G mismatch. The cell's DNA replication machinery recognizes the U as a T, and hence C:G is converted to a T:A base pair. During germinal center development of B lymphocytes, AID also generates other types of mutations, such as C:G to A:T. The mechanism by which these other mutations are created is not well understood.


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