SCUBA

MBOAT7 — Membrane bound O-acyltransferase domain containing 7

MBOAT7 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.

MBOAT7's module in each cell type

Cell typeModuleShares the module with
Hematopoietic progenitor cellsCytoskeletal Remodeling
Cytoskeletal
AHNAK, ANXA1, ATP2B1, DPYSL3, FHL1, IDS, MTURN, PBXIP1 +5 more
Innate lymphoid cellsLymphocyte Apoptosis Regulation
Immune regulation
ANP32B, ARMCX3, CCDC69, CHD2, DHRS7, ELF1, FXYD5, GLIPR1 +14 moreView in SCUBA
MacrophagesER Protein Translocation
Vesicular traficking
ACADVL, ARRB2, BCL7B, BORCS7, DDRGK1, DEF8, DNAJB12, DVL3 +22 moreView in SCUBA
NeutrophilsTLR Lipid Signaling
Innate immunity
DGAT2, IFNAR1, LILRB3, NOTCH1, PPP1R3B, STEAP4, TLR1, TLR4 +1 more

About the gene

SynonymsBB1, hMBOA-7, LENG4, LPIAT1, LPLAT, LPLAT11
Chromosome19: 54173412-54189882
Predicted locationMembrane
Essential geneNo
Protein classDisease related genes, Human disease related genes, Metabolic proteins, Potential drug targets, Predicted membrane proteins, Transporters
Molecular functionAcyltransferase, Transferase
Biological processLipid biosynthesis, Lipid metabolism, Phospholipid biosynthesis, Phospholipid metabolism

Function

Acyltransferase which catalyzes the transfer of an acyl group from an acyl-CoA to a lysophosphatidylinositol (1- acylglycerophosphatidylinositol or LPI) leading to the production of a phosphatidylinositol (1,2-diacyl-sn-glycero-3-phosphoinositol or PI) and participates in the reacylation step of the phospholipid remodeling pathway also known as the Lands cycle. Prefers arachidonoyl-CoA as the acyl donor, thus contributing to the regulation of free levels arachidonic acid in cell. In liver, participates in the regulation of triglyceride metabolism through the phosphatidylinositol acyl-chain remodeling regulation.

Human Protein Atlas · Open Targets · UniProt

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