SCUBA

APOBEC3G — Apolipoprotein B mRNA editing enzyme catalytic subunit 3G

APOBEC3G belongs to a gene co-expression module in 6 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

APOBEC3G's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsInterferon-stimulated genes
Anti-viral
ARPC4, ARPC5L, BAK1, BST2, DCTN3, ECH1, ETFB, FAM104A +14 moreView in SCUBA
Gamma-delta T cellsEffector Cell Migration
migration & adhesion
ADAM15, ADAM8, ANXA2, CD52, CTSC, DSTN, FUT11, GLIPR2 +17 more
Innate lymphoid cellsNK Homing Circulating
Homing & TEM
ADD3, ANXA1, C16orf54, C1orf162, CAPG, CASP4, CAST, CDKN2D +37 moreView in SCUBA
MonocytesInflammasome Activation
Innate immunity
AIM2, ARID5B, BATF3, BST2, CASP5, CD47, CNDP2, CYSTM1 +4 moreView in SCUBA
Mucosal-associated invariant T cellMature Effector MAIT
T cell maturation
ADD3, ANTKMT, CCL5, CXXC5, FHL3, GZMK, ITGA6, ITGB2 +7 more
Natural Killer cellsNK Cytotoxic Signaling
Cytotoxicity
B2M, CALM1, CD48, GLIPR2, HCST, MYL12A, TMSB10, TRGC1 +1 moreView in SCUBA

About the gene

SynonymsbK150C2.7, CEM15, dJ494G10.1, FLJ12740, MDS019
Chromosome22: 39077067-39087743
Predicted locationIntracellular
Essential geneNo
Protein classEnzymes, Predicted intracellular proteins
Molecular functionHydrolase
Biological processAntiviral defense, Host-virus interaction, Immunity, Innate immunity

Function

DNA deaminase (cytidine deaminase) which acts as an inhibitor of retrovirus replication and retrotransposon mobility via deaminase- dependent and -independent mechanisms. Exhibits potent antiviral activity against Vif-deficient HIV-1. After the penetration of retroviral nucleocapsids into target cells of infection and the initiation of reverse transcription, it can induce the conversion of cytosine to uracil in the minus-sense single-strand viral DNA, leading to G-to-A hypermutations in the subsequent plus-strand viral DNA. The resultant detrimental levels of mutations in the proviral genome, along with a deamination-independent mechanism that works prior to the proviral integration, together exert efficient antiretroviral effects in infected target cells. Selectively targets single-stranded DNA and does not deaminate double-stranded DNA or single- or double-stranded RNA. Exhibits antiviral activity also against simian immunodeficiency viruses (SIVs), hepatitis B virus (HBV), equine infectious anemia virus (EIAV), xenotropic MuLV-related virus (XMRV) and simian foamy virus (SFV). May inhibit the mobility of LTR and non-LTR retrotransposons.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.