A disintegrin and metalloproteinase with thrombospondin motifs 17 isof - Protein

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Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

Characteristics and genotype-phenotype correlations in ADAMTS17 mutation-related Weill-Marchesani syndrome. [Exp Eye Res. 2023]
Characteristics and genotype-phenotype correlations in ADAMTS17 mutation-related Weill-Marchesani syndrome.
Guo D, Liu L, Yang F, Young CA, Zheng D, Jin G. Exp Eye Res. 2023 Sep; 234:109606. Epub 2023 Jul 26.
A common variant rs2054564 in ADAMST17 is associated with susceptibility to lumbar spondylosis. [Sci Rep. 2023]
A common variant rs2054564 in ADAMST17 is associated with susceptibility to lumbar spondylosis.
Taniguchi Y, Akune T, Nishida N, Omori G, Ha K, Ueno K, Saito T, Oichi T, Koike A, Mabuchi A, et al. Sci Rep. 2023 Mar 25; 13(1):4900. Epub 2023 Mar 25.
A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features. [Sci Rep. 2020]
A novel pathogenic missense ADAMTS17 variant that impairs secretion causes Weill-Marchesani Syndrome with variably dysmorphic hand features.
Evans DR, Green JS, Fahiminiya S, Majewski J, Fernandez BA, Deardorff MA, Johnson GJ, Whelan JH, Hubmacher D, Apte SS, et al. Sci Rep. 2020 Jul 2; 10(1):10827. Epub 2020 Jul 2.

RefSeq genomic sequence
See the genomic reference sequence for the ADAMTS17 gene (NG_016287.2).
RefSeq mRNA
See reference mRNA sequence for the ADAMTS17 gene (XM_054377430.1).
RefSeq protein isoforms
See 35 reference sequence protein isoforms for the ADAMTS17 gene.