SCUBA

AKT3 — AKT serine/threonine kinase 3

AKT3 belongs to a gene co-expression module in 4 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.

AKT3's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsGIMAP survival
Immune regulation
ABLIM1, ANKRD13D, ARL4C, C16orf54, CA5B, COPA, CRBN, DYNLT1 +16 moreView in SCUBA
Gamma-delta T cellsInnate Stress Signaling
Inflammation
B4GALT4, BCR, BLOC1S4, COL6A2, CREBRF, DGKQ, ELF2, FAM53B +23 more
Mucosal-associated invariant T cellCalcineurin-NFAT Signaling
TCR Signaling
CDC14A, IQGAP2, NCALD, NEK7, PLCB1, PLCL2, PPP2R2B, PPP3CA +3 more
Natural Killer cellsNK Cell Activation
activation
AHNAK, ANXA1, C16orf54, C1orf162, CD226, CD300A, ITGAX, PLAC8 +2 moreView in SCUBA

About the gene

SynonymsPKBG, PRKBG, RAC-gamma
Chromosome1: 243488233-243851079
Predicted locationIntracellular
Essential geneNo
Protein classCancer-related genes, Disease related genes, Enzymes, Human disease related genes, Plasma proteins, Potential drug targets, Predicted intracellular proteins, RAS pathway related proteins
Molecular functionKinase, Serine/threonine-protein kinase, Transferase

Function

AKT3 is one of 3 closely related serine/threonine-protein kinases (AKT1, AKT2 and AKT3) called the AKT kinase, and which regulate many processes including metabolism, proliferation, cell survival, growth and angiogenesis. This is mediated through serine and/or threonine phosphorylation of a range of downstream substrates. Over 100 substrate candidates have been reported so far, but for most of them, no isoform specificity has been reported. AKT3 is the least studied AKT isoform. It plays an important role in brain development and is crucial for the viability of malignant glioma cells. AKT3 isoform may also be the key molecule in up-regulation and down-regulation of MMP13 via IL13. Required for the coordination of mitochondrial biogenesis with growth factor-induced increases in cellular energy demands. Down- regulation by RNA interference reduces the expression of the phosphorylated form of BAD, resulting in the induction of caspase- dependent apoptosis.

Human Protein Atlas · Open Targets · UniProt

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