SCUBA

ACAA2 — Acetyl-CoA acyltransferase 2

ACAA2 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.

ACAA2's module in each cell type

Cell typeModuleShares the module with
EnterocytesCore energy metabolism
Mitochondrial & OxPhos
CFL1, CYCS, GAPDH, ME2, P4HB, PPA1, PSME2, SOD1View in SCUBA
Gamma-delta T cellsGlycolysis & Proteasome
Housekeeping
ANAPC15, APEH, C1QBP, CCDC167, CHMP2A, CLNS1A, ENO1, HINT1 +11 more
Goblet cellsColonocyte Metabolic Defense
Mitochondrial & OxPhos
CAT, CRYBG1, GLIPR2, MLXIP, PKDCC, SAMD5, SEMA6A, ZFHX3View in SCUBA
Innate lymphoid cellsNK Cytotoxic Effector
Cytotoxicity
APIP, B4GALNT1, CAMK4, CCL5, CCNG2, CD247, CD3E, DCXR +17 moreView in SCUBA
Mucosal-associated invariant T cellType I Interferon
Inflammation
ABCF2, ANXA2R, BST2, CHST12, IRF9, LY6E, LYSMD2, NDUFC2 +6 more
Smooth muscle cellsSMC Contractile Signaling
Contractility
BOC, CELF2, PLEKHO1, PRUNE2, RGS2, SCARA3, SDC3View in SCUBA

About the gene

SynonymsDSAEC
Chromosome18: 49782164-49813953
Predicted locationIntracellular
Essential geneNo
Protein classEnzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
Molecular functionAcyltransferase, Hydrolase, Transferase
Biological processFatty acid metabolism, Lipid metabolism

Function

In the production of energy from fats, this is one of the enzymes that catalyzes the last step of the mitochondrial beta- oxidation pathway, an aerobic process breaking down fatty acids into acetyl-CoA (Probable). Using free coenzyme A/CoA, catalyzes the thiolytic cleavage of medium- to long-chain unbranched 3-oxoacyl-CoAs into acetyl-CoA and a fatty acyl-CoA shortened by two carbon atoms (Probable). Also catalyzes the condensation of two acetyl-CoA molecules into acetoacetyl-CoA and could be involved in the production of ketone bodies (Probable). Also displays hydrolase activity on various fatty acyl-CoAs. Thereby, could be responsible for the production of acetate in a side reaction to beta-oxidation (Probable). Abolishes BNIP3-mediated apoptosis and mitochondrial damage.

Human Protein Atlas · Open Targets · UniProt

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