SCUBA

ABHD12 — Abhydrolase domain containing 12, lysophospholipase

ABHD12 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.

ABHD12's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsGlycosylation & trafficking
Protein processing & ER
AASDHPPT, ACTR1A, ANKRD35, AP1S1, ARRDC1, ATF6B, ATG5, CDK19 +25 moreView in SCUBA
EnterocytesBrush border lipid handling
Absorption
ABCG1, ARL14, CDHR2, ENTPD8, IDS, PNPLA2, RAI14, SEMA3G +2 moreView in SCUBA
Gamma-delta T cellsTGF-beta Signaling
Immune regulation
ABCF1, ACAP2, ADIPOR2, CBX6, ENPP4, FBXO9, GSAP, INPP4A +18 more
MacrophagesEfferocytosis Anti-inflammatory
Lysosomal & pahgocytosis
ADGRG5, AIG1, AXL, CCS, CD101, CD1D, CD300A, EVA1B +18 moreView in SCUBA

About the gene

SynonymsABHD12A, BEM46L2, C20orf22, dJ965G21.2, DKFZP434P106
Chromosome20: 25294742-25390835
Predicted locationIntracellular, Membrane
Essential geneNo
Protein classDisease related genes, Enzymes, Human disease related genes, Metabolic proteins, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins
Molecular functionHydrolase
Biological processLipid metabolism

Function

Lysophosphatidylserine (LPS) lipase that mediates the hydrolysis of lysophosphatidylserine, a class of signaling lipids that regulates immunological and neurological processes. Represents a major lysophosphatidylserine lipase in the brain, thereby playing a key role in the central nervous system (By similarity). Also able to hydrolyze oxidized phosphatidylserine; oxidized phosphatidylserine is produced in response to severe inflammatory stress and constitutes a proapoptotic 'eat me' signal. Also has monoacylglycerol (MAG) lipase activity: hydrolyzes 2-arachidonoylglycerol (2-AG), thereby acting as a regulator of endocannabinoid signaling pathways. Has a strong preference for very-long-chain lipid substrates; substrate specificity is likely due to improved catalysis and not improved substrate binding.

Human Protein Atlas · Open Targets · UniProt

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