ADAMTS9

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ADAMTS9
Identifiers
AliasesADAMTS9, ADAM metallopeptidase with thrombospondin type 1 motif 9
External IDsOMIM: 605421 MGI: 1916320 HomoloGene: 18821 GeneCards: ADAMTS9
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_182920
NM_001318781
NM_020249
NM_182921

NM_175314

RefSeq (protein)

NP_001305710
NP_891550

n/a

Location (UCSC)Chr 3: 64.52 – 64.69 MbChr 6: 92.75 – 92.92 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

A disintegrin and metalloproteinase with thrombospondin motifs 9 is an enzyme that in humans is encoded by the ADAMTS9 gene.[5][6]

This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family 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. Members of the ADAMTS family have been implicated in the cleavage of proteoglycans, the control of organ shape during development, and the inhibition of angiogenesis. This gene is localized to chromosome 3p14.3-p14.2, an area known to be lost in hereditary renal tumors.[6]

References[]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000163638 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030022 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Clark ME, Kelner GS, Turbeville LA, Boyer A, Arden KC, Maki RA (Sep 2000). "ADAMTS9, a novel member of the ADAM-TS/ metallospondin gene family". Genomics. 67 (3): 343–50. doi:10.1006/geno.2000.6246. PMID 10936055.
  6. ^ a b "Entrez Gene: ADAMTS9 ADAM metallopeptidase with thrombospondin type 1 motif, 9".

Further reading[]

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