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Gene : ADAMTS17 Homo sapiens

Name  ? ADAM metallopeptidase with thrombospondin type 1 motif 17 Cytological Location  15q26.3
Brief Description  ADAM metallopeptidase with thrombospondin type 1 motif 17
description  This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The encoded preproprotein is proteolytically processed to generate the mature protein, which may promote breast cancer cell growth and survival. Mutations in this gene are associated with a Weill-Marchesani-like syndrome, which is characterized by lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature. [provided by RefSeq, May 2016]
  • synonyms:
  • OTTHUMG00000149867,
  • NM_139057,
  • uc002bvv.2,
  • FLJ16363,
  • AJ315735,
  • a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 17,
  • ADAMTS17,
  • WMS4,
  • FLJ32769,
  • HGNC:17109
  • identifiers:
  • 170691,
  • ENSG00000140470,
  • ADAMTS17

Genome feature

Region: gene ? Length: 371487  
Location: 15:99971438-100342924 reverse strand Cyto location: 15q26.3


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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

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Proteins

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SNPs

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Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

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Other

2011 SN Ps

5 Cross References

17 Data Sets

29 Homologues

0 Located Features

90 Rna Seq Results