SCUBA

LDLRAP1 — Low density lipoprotein receptor adaptor protein 1

LDLRAP1 belongs to a gene co-expression module in 3 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.

LDLRAP1's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsNaive T cell
T cell development
AIF1, AK5, APBA2, BEND5, BEX2, C1orf162, CBR3, CYSLTR1 +21 moreView in SCUBA
CD8⁺ T cellsNaive/Central Memory
T cell maturation
AIF1, ATM, CCR7, FCMR, FOXP1, KLF2, KLF3, LEF1 +7 moreView in SCUBA
Gamma-delta T cellsDeath Receptor Apoptosis
Stress
CXCR3, FHL3, GABARAPL2, LY6E, PDGFB, PLSCR3, SGSM3, SHISAL2A +4 more

About the gene

SynonymsARH, ARH2, DKFZp586D0624, FHCB1, FHCB2, MGC34705
Chromosome1: 25543606-25568886
Predicted locationIntracellular
Essential geneNo
Protein classDisease related genes, Human disease related genes, Predicted intracellular proteins
Biological processCholesterol metabolism, Endocytosis, Lipid metabolism, Steroid metabolism, Sterol metabolism

Function

Adapter protein (clathrin-associated sorting protein (CLASP)) required for efficient endocytosis of the LDL receptor (LDLR) in polarized cells such as hepatocytes and lymphocytes, but not in non- polarized cells (fibroblasts). May be required for LDL binding and internalization but not for receptor clustering in coated pits. May facilitate the endocytosis of LDLR and LDLR-LDL complexes from coated pits by stabilizing the interaction between the receptor and the structural components of the pits. May also be involved in the internalization of other LDLR family members. Binds to phosphoinositides, which regulate clathrin bud assembly at the cell surface. Required for trafficking of LRP2 to the endocytic recycling compartment which is necessary for LRP2 proteolysis, releasing a tail fragment which translocates to the nucleus and mediates transcriptional repression (By similarity).

Human Protein Atlas · Open Targets · UniProt

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