Entity Details

Primary name ATS17_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8TE56
EntryNameATS17_HUMAN
FullNameA disintegrin and metalloproteinase with thrombospondin motifs 17
TaxID9606
Evidenceevidence at transcript level
Length1095
SequenceStatuscomplete
DateCreated2003-02-28
DateModified2021-06-02

Ontological Relatives

GenesADAMTS17

GO terms

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GOName
GO:0004222 metalloendopeptidase activity
GO:0005576 extracellular region
GO:0030198 extracellular matrix organization
GO:0031012 extracellular matrix
GO:0046872 metal ion binding

Subcellular Location

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Subcellular Location
Secreted

Domains

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DomainNameCategoryType
IPR000884 Thrombospondin type-1 (TSP1) repeatRepeatRepeat
IPR001590 Peptidase M12B, ADAM/reprolysinDomainDomain
IPR002870 Peptidase M12B, propeptideDomainDomain
IPR006586 ADAM, cysteine-rich domainDomainDomain
IPR010294 ADAM-TS Spacer 1DomainDomain
IPR010909 PLACDomainDomain
IPR013087 Zinc finger C2H2-typeDomainDomain
IPR013273 ADAMTS/ADAMTS-likeFamilyFamily
IPR024079 Metallopeptidase, catalytic domain superfamilyFamilyHomologous superfamily
IPR036383 Thrombospondin type-1 (TSP1) repeat superfamilyFamilyHomologous superfamily
IPR041645 ADAM cysteine-rich domain 2DomainDomain

Diseases

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Disease IDSourceNameDescription
613195 OMIMWeill-Marchesani syndrome 4 (WMS4)An autosomal recessive syndrome characterized by lenticular myopia, ectopia lentis, glaucoma, spherophakia and short stature. Brachydactyly and decreased joint flexibility are present in some patients. The disease is caused by variants affecting the gene represented in this entry.

Interactions

0 interactions

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