Entity Details

Primary name ADAMTS17
Entity type gene
Source Source Link

Details

PrimaryID170691
RefseqGeneNG_016287
SymbolADAMTS17
NameADAM metallopeptidase with thrombospondin type 1 motif 17
Chromosome15
Location15q26.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-02-13
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsATS17_HUMAN

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

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

2 interactions

InteractorPartnerSourcesPublicationsLink
ADAMTS17CUL1BioGRID, IntAct21145461 details
ADAMTS17ATL3BioGRID, IntAct30021884 details