Contents

ADAMTS10

Protein-coding gene in the species Homo sapiens

ADAMTS10
Identifiers
Aliases	ADAMTS10, ADAM-TS10, ADAMTS-10, WMS, WMS1, ADAM metallopeptidase with thrombospondin type 1 motif 10
External IDs	OMIM: 608990; MGI: 2449112; HomoloGene: 81940; GeneCards: ADAMTS10; OMA:ADAMTS10 - orthologs
Gene location (Human) Chr. Chromosome 19 (human)[1] Band 19p13.2 Start 8,580,240 bp[1] End 8,610,735 bp[1]
Gene location (Mouse) Chr. Chromosome 17 (mouse)[2] Band 17|17 B1 Start 33,743,178 bp[2] End 33,772,756 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in Descending thoracic aorta right coronary artery skin of arm ascending aorta nasal epithelium myocardium of left ventricle granulocyte cardiac muscle tissue of right atrium cerebellar vermis vena cava Top expressed in ascending aorta aortic valve granulocyte left lung left lung lobe tail of embryo external carotid artery internal carotid artery genital tubercle cerebellar cortex More reference expression data BioGPS More reference expression data
Gene ontology Molecular function peptidase activity metalloendopeptidase activity protein binding hydrolase activity metallopeptidase activity metal ion binding molecular function Cellular component microfibril extracellular region extracellular matrix collagen-containing extracellular matrix Biological process proteolysis biological process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 81794 224697 Ensembl ENSG00000142303 ENSMUSG00000024299 UniProt Q9H324 P58459 RefSeq (mRNA) NM_001282352 NM_030957 NM_172619 NM_001329143 NM_001329147 NM_001329151 NM_001329152 NM_001329153 NM_001329154 NM_001329202 NM_001329203 RefSeq (protein) NP_001269281 NP_112219 NP_001316072 NP_001316076 NP_001316080 NP_001316081 NP_001316082 NP_001316083 NP_001316131 NP_001316132 NP_766207 Location (UCSC) Chr 19: 8.58 – 8.61 Mb Chr 17: 33.74 – 33.77 Mb PubMed search [3] [4]
Wikidata
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A disintegrin and metalloproteinase with thrombospondin motifs 10 is an enzyme that in humans is encoded by the ADAMTS10 gene.^[5]

This gene belongs to the ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin type-1 motifs) family of zinc-dependent proteases. ADAMTS proteases are complex secreted enzymes containing a prometalloprotease domain of the reprolysin type attached to an ancillary domain with a highly conserved structure that includes at least one thrombospondin type 1 repeat. They have been demonstrated to have important roles in connective tissue organization, coagulation, inflammation, arthritis, angiogenesis and cell migration. The product of this gene plays a major role in growth and in skin, lens, and heart development. It is also a candidate gene for autosomal recessive Weill-Marchesani syndrome.^[5]

References[edit]

Further reading[edit]

External links[edit]

• GeneReviews/NIH/NCBI/UW entry on Weill-Marchesani Syndrome
• The MEROPS online database for peptidases and their inhibitors: M12.235
• Human ADAMTS10 genome location and ADAMTS10 gene details page in the UCSC Genome Browser.

This article on a gene on human chromosome 19 is a stub. You can help Wikipedia by expanding it.