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Gene : AICDA Homo sapiens

Name  ? activation induced cytidine deaminase Cytological Location  12p13.31
Brief Description  activation induced cytidine deaminase
description  This gene encodes a RNA-editing deaminase that is a member of the cytidine deaminase family. The protein is involved in somatic hypermutation, gene conversion, and class-switch recombination of immunoglobulin genes. Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). [provided by RefSeq, Feb 2009]
  • synonyms:
  • HIGM2,
  • AB040430,
  • OTTHUMG00000168676,
  • HIGM2,
  • AID,
  • CDA2,
  • HEL-S-284,
  • HGNC:13203,
  • CDA2,
  • AICDA,
  • uc001qur.3,
  • NM_020661,
  • ARP2,
  • AID,
  • activation-induced cytidine deaminase,
  • ARP2
  • identifiers:
  • 57379,
  • ENSG00000111732,
  • AICDA

Genome feature

Region: gene ? Length: 10805  
Location: 12:8602166-8612970 reverse strand Cyto location: 12p13.31


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

0 SN Ps

5 Cross References

18 Data Sets

12 Homologues

0 Located Features

90 Rna Seq Results