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Proteins/UNIPROT:Q8TE56

ADAMTS17

Protein·UNIPROT:Q8TE56

Open in the graph

Extracellular metalloprotease that regulates skeletal development by modulating BMP-SMAD signaling and extracellular matrix microfibril organization, which controls chondrocyte differentiation and bone growth..

Function from UniProtKB (Q8TE56), read 2026-09-23. CC BY 4.0.

Curated compounds routed: 0

What the reference databases state

Inferred

Inferred — not reported by a source. Evidence key

GenCC submitters' classifications

1 row

Weill-Marchesani 4 syndrome, recessive has a germline basis in ADAMTS17DiseaseGenCC HGNC:17109|MONDO:0013176Inferred only

Statements

11 statements

11 statements · 2 reference databases · Subject: ADAMTS17 · Sources: Hetionet, Reactome

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NCKAP5L covaries with ADAMTS17ProteinHetionet hetionet:covaries:170691-57701Inferred only
CUL1 interacts with ADAMTS17ProteinHetionet hetionet:interacts:170691-8454Inferred only
ADAMTS17 participates in Defective B3GALTL causes PpSPathwayReactome R-HSA-5083635Inferred only
ADAMTS17 participates in DiseasePathwayReactome R-HSA-1643685Inferred only
ADAMTS17 participates in Diseases associated with O-glycosylation of proteinsPathwayReactome R-HSA-3906995Inferred only
ADAMTS17 participates in Diseases of glycosylationPathwayReactome R-HSA-3781865Inferred only
ADAMTS17 participates in Diseases of metabolismPathwayReactome R-HSA-5668914Inferred only
ADAMTS17 participates in Metabolism of proteinsPathwayReactome R-HSA-392499Inferred only
ADAMTS17 participates in O-glycosylation of TSR domain-containing proteinsPathwayReactome R-HSA-5173214Inferred only
ADAMTS17 participates in O-linked glycosylationPathwayReactome R-HSA-5173105Inferred only
ADAMTS17 participates in Post-translational protein modificationPathwayReactome R-HSA-597592Inferred only

Other names

3 names

Resolves to: ADAMTS17

Also called: ADAM-TS 17ADAM-TS17ADAMTS-17

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