SCUBA

ADAM10 — ADAM metallopeptidase domain 10

ADAM10 belongs to a gene co-expression module in 6 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.

ADAM10's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsChromatin transcription regulation
DNA/chromatin regulation
CIRBP, CLIP1, CUL9, GRPEL2, HBP1, KDM2A, NCOA3, NSD3 +10 moreView in SCUBA
EndothelialTGF-beta ECM Remodeling
ECM remodeling
APLP2, CCNDBP1, CYB5R3, DHRS3, EFEMP2, GNAS, HIPK2, MGST2 +10 moreView in SCUBA
Gamma-delta T cellsT Cell Identity Program
T cell maturation
ADA2, ARHGAP12, ATM, LPP, NLRC5, PIKFYVE, PJA2, PRKCQ +5 more
Lymphatic endothelialEndosomal Vesicle Trafficking
Housekeeping
APC, APP, ATP9A, GLG1, MTR, NCOA3, PCNX4, PDCD6IP +5 moreView in SCUBA
MacrophagesHypoxia-driven Activation
Inflammatory
ACVR1B, ADAM9, ALCAM, ANO6, B3GNT2, BTG1, C5AR1, CAB39 +33 moreView in SCUBA
Mucosal-associated invariant T cellIL-18 Innate Activation
Inflammation
COLQ, IL18RAP, KIF5C, ME1, MYBL1, NEO1, P2RY14, PARP8 +3 more

About the gene

SynonymsCD156C, HsT18717, kuz, MADM
Chromosome15: 58588809-58749791
Predicted locationIntracellular, Membrane
Essential geneNo
Protein classCancer-related genes, CD markers, Disease related genes, Enzymes, Human disease related genes, Plasma proteins, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins, Transporters
Molecular functionHydrolase, Metalloprotease, Protease
Biological processNotch signaling pathway

Function

Transmembrane metalloprotease which mediates the ectodomain shedding of a myriad of transmembrane proteins, including adhesion proteins, growth factor precursors and cytokines being essential for development and tissue homeostasis. Associates with six members of the tetraspanin superfamily TspanC8 which regulate its exit from the endoplasmic reticulum and its substrate selectivity. Cleaves the membrane-bound precursor of TNF-alpha at '76-Ala-|-Val-77' to its mature soluble form. Responsible for the proteolytical release of soluble JAM3 from endothelial cells surface. Responsible for the proteolytic release of several other cell-surface proteins, including heparin-binding epidermal growth-like factor, ephrin-A2, CD44, CDH2 and for constitutive and regulated alpha- secretase cleavage of amyloid precursor protein (APP). Contributes to the normal cleavage of the cellular prion protein. Involved in the cleavage of the adhesion molecule L1 at the cell surface and in released membrane vesicles, suggesting a vesicle-based protease activity. Also controls the proteolytic processing of Notch and mediates lateral inhibition during neurogenesis (By similarity). Required for the development of type 1 transitional B cells into marginal zone B cells, probably by cleaving Notch (By similarity). Responsible for the FasL ectodomain shedding and for the generation of the remnant ADAM10-processed FasL (FasL APL) transmembrane form. Also cleaves the ectodomain of the integral membrane proteins CORIN and ITM2B. Mediates the proteolytic cleavage of LAG3, leading to release the secreted form of LAG3 (By similarity). Mediates the proteolytic cleavage of IL6R and IL11RA, leading to the release of secreted forms of IL6R and IL11RA. Enhances the cleavage of CHL1 by BACE1 (By similarity). Cleaves NRCAM (By similarity). Cleaves TREM2, resulting in shedding of the TREM2 ectodomain. Involved in the development and maturation of glomerular and coronary vasculature (By similarity). During development of the cochlear organ of Corti, promotes pillar cell separation by forming a ternary complex with CADH1 and EPHA4 and cleaving CADH1 at adherens junctions (By similarity). May regulate the EFNA5-EPHA3 signaling. Regulates leukocyte transmigration as a sheddase for the adherens junction protein VE- cadherin/CDH5 in endothelial cells. (Microbial infection) Promotes the cytotoxic activity of S.aureus hly by binding to the toxin at zonula adherens and promoting formation of toxin pores.

Human Protein Atlas · Open Targets · UniProt

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