SCUBA

PLTP — Phospholipid transfer protein

PLTP 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.

PLTP's module in each cell type

Cell typeModuleShares the module with
FibroblastsElastic Fiber ECM
ECM production
ADD3, ASPA, FBLN5, FRMD3, SLC29A1, SLIT2, SVEP1, TNXBView in SCUBA
MacrophagesResident Mac Identity
Tissue homeostasis
ACVRL1, CCND1, CD200R1, CFD, CR1, CTSF, EMB, EPHX1 +16 moreView in SCUBA
MonocytesTissue-Resident Macrophage
Tissue adaptation
DAB2, ETV5, FOLR2, FRMD4A, GPNMB, ITGB5, LGMN, LILRB5 +7 moreView in SCUBA
Smooth muscle cellsFibroblast Matrisome
ECM remodeling
ADAMDEC1, EMP1, FBLN1, LTBP4, NR2F1, PROCR, RGS10, S100A10 +1 moreView in SCUBA

About the gene

SynonymsBPIFE
Chromosome20: 45898621-45912155
Predicted locationIntracellular, Secreted
Essential geneNo
Protein classPlasma proteins, Predicted intracellular proteins, Predicted secreted proteins, Transporters
Biological processLipid transport, Transport

Function

Mediates the transfer of phospholipids and free cholesterol from triglyceride-rich lipoproteins (low density lipoproteins or LDL and very low density lipoproteins or VLDL) into high-density lipoproteins (HDL) as well as the exchange of phospholipids between triglyceride-rich lipoproteins themselves. Facilitates the transfer of a spectrum of different lipid molecules, including diacylglycerol, phosphatidic acid, sphingomyelin, phosphatidylcholine, phosphatidylinositol, phosphatidylglycerol, cerebroside and phosphatidyl ethanolamine. Plays an important role in HDL remodeling which involves modulating the size and composition of HDL. Also plays a key role in the uptake of cholesterol from peripheral cells and tissues that is subsequently transported to the liver for degradation and excretion. Two distinct forms of PLTP exist in plasma: an active form that can transfer phosphatidylcholine from phospholipid vesicles to HDL, and an inactive form that lacks this capability.

Human Protein Atlas · Open Targets · UniProt

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