SCUBA

THBS1 — Thrombospondin 1

THBS1 belongs to a gene co-expression module in 9 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.

THBS1's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsEffector activation NFkB
TCR/AP1/NFKb pathway
ADAM19, AHR, ARFGAP3, ATF5, BHLHE40, CGAS, DUSP5, ETF1 +23 moreView in SCUBA
EndothelialProcoagulant TGF-β Response
Inflammation
CITED4, CSF3, EHD1, F3, LAMC1, LIPG, MED24, PLEKHO1 +7 moreView in SCUBA
FibroblastsCytokine Inflammatory Response
Inflammatory
CXCL2, DNAJB4, GFPT2, HES4, MAP3K8, MMP19, RASL11A, RGCC +4 moreView in SCUBA
Glial cellsRNA Splicing Processing
RNA processing & translation
DDX3X, DDX5, HNRNPA2B1, HNRNPAB, HNRNPDL, HNRNPH1, MAFB, NES +2 moreView in SCUBA
Goblet cellsNotch Secretory Specification
Epithelial development
EDN1, EREG, FKBP1A, GPRC5C, HES4, HES5, MYC, NOTCH2 +4 moreView in SCUBA
MacrophagesLipid-Sensing Transcriptional
Lipid metabolism
ANKLE2, BAIAP2, C19orf25, C1orf52, COX19, CWC25, DEDD2, DNTTIP2 +29 moreView in SCUBA
MonocytesIgA-Monocyte Activation
Innate immunity
AATK, AREG, ASPH, ATP2A3, CD82, FCAR, NIBAN2, SERPINB2 +3 moreView in SCUBA
PericytesCytokine Inflammatory Response
Inflammatory
ADAMTS4, C11orf96, CEBPB, CEBPD, GEM, ID4, KCNE4, PHLDA1 +4 moreView in SCUBA
Smooth muscle cellsNF-kB Stress Response
Stress
BHLHE40, CCNL1, FADS3, HSP90AB1, IER3, MIDN, NFKBIZ, PPP1R15A +1 moreView in SCUBA

About the gene

SynonymsTHBS, THBS-1, TSP, TSP-1, TSP1
Chromosome15: 39581079-39599466
Predicted locationSecreted
Essential geneNo
Protein classCancer-related genes, Candidate cardiovascular disease genes, Plasma proteins, Predicted secreted proteins
Molecular functionHeparin-binding
Biological processAngiogenesis, Apoptosis, Cell adhesion, Inflammatory response, Unfolded protein response

Function

Adhesive glycoprotein that mediates cell-to-cell and cell-to- matrix interactions. Multifunctional, involved in inflammation, angiogenesis, wound healing, reactive oxygen species (ROS) signaling, nitrous oxide (NO) signaling, apoptosis, senescence, aging, cellular self-renewal, stemness, and cardiovascular and metabolic homeostasis. Negatively modulates dendritic cell activation and cytokine release, as part of an autocrine feedback loop, contributing to the resolution of inflammation and immune homeostasis. Ligand for receptor CD47. Modulates nitrous oxide (NO) signaling via CD47, hence playing a role as a pressor agent, supporting blood pressure (By similarity). Plays a role in endothelial cell senescence, acting via CD47, by increasing the abundance and activation of NADPH oxidase NOX1, and so generating excess ROS. Inhibits stem cell self-renewal, acting via CD47 signaling, probably by regulation of the stem cell transcription factors POU5F1/OCT4, SOX2, MYC/c-Myc and KLF4 (By similarity). Negatively modulates wound healing, acting via CD47 (By similarity). Ligand for receptor CD36. Involved in inducing apoptosis in podocytes in response to elevated free fatty acids, acting via CD36 (By similarity). Plays a role in suppressing angiogenesis, acting, depending on context, via CD36 or CD47. Promotes cellular senescence in a TP53-CDKN1A-RB1 signaling-dependent manner. Ligand for immunoglobulin-like cell surface receptor SIRPA. Involved in ROS signaling in non- phagocytic cells, stimulating NADPH oxidase-derived ROS production, acting via interaction with SIRPA. Plays a role in metabolic dysfunction in diet-induced obesity, perhaps acting by exacerbating adipose inflammatory activity; its effects may be mediated, at least in part, through enhanced adipocyte proliferation (By similarity). Plays a role in ER stress response, via its interaction with the activating transcription factor 6 alpha (ATF6) which produces adaptive ER stress response factors (By similarity). May be involved in age-related conditions, including metabolic dysregulation, during normal aging.

Human Protein Atlas · Open Targets · UniProt

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