AICDA

Description		activation induced cytidine deaminase
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GO Annotations	Cellular Component	P-body Nucleus Cytoplasm Protein-containing Complex
	Molecular Function	RNA Binding Cytidine Deaminase Activity Protein Binding Zinc Ion Binding Ubiquitin Protein Ligase Binding Identical Protein Binding Deoxycytidine Deaminase Activity
	Biological Process	MRNA Processing Cytidine Deamination Negative Regulation Of Transposition Somatic Diversification Of Immunoglobulins Somatic Hypermutation Of Immunoglobulin Genes Cytidine To Uridine Editing B Cell Differentiation Regulation Of Nuclear Cell Cycle DNA Replication Defense Response To Bacterium Isotype Switching Negative Regulation Of Single Stranded Viral RNA Replication Via Double Stranded DNA Intermediate Defense Response To Virus DNA Cytosine Deamination Cellular Response To Lipopolysaccharide DNA Demethylation Negative Regulation Of Methylation-dependent Chromatin Silencing
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Drugs
Diseases		Hyper IgM syndromes, autosomal recessive type, including the following three diseases: Activation-induced cytidine deaminase (AICD) defect; Uracil nucleotide glycoside glycosylase (UNG) defect; Immunodeficiency with hyper-IgM type 3
GWAS		Takayasu arteritis ( 25604533)
Interacting Genes		6 interacting genes: APP NEDD4L PRKDC PSME3 RNF126 RPA1
Entrez ID		57379
HPRD ID		05585
Ensembl ID		ENSG00000111732
Uniprot IDs		Q546Y9 Q6QJ80 Q7Z599 Q9GZX7
PDB IDs		5JJ4 5W0R 5W0U 5W0Z 5W1C
Enriched GO Terms of Interacting Partners?
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