PREDICTED: Homo sapiens ADAM metallopeptidase with thrombospondin type - Nucleotide

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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.
The role of ADAMTS6 and ADAMTS17 polymorphisms in susceptibility to lumbar disc herniation in Chinese Han population. [Eur Spine J. 2023]
The role of ADAMTS6 and ADAMTS17 polymorphisms in susceptibility to lumbar disc herniation in Chinese Han population.
Han P, Jiang F, Zhang L. Eur Spine J. 2023 Apr; 32(4):1106-1114. Epub 2023 Feb 21.

RefSeq alternative splicing
See 35 reference mRNA sequence splice variants for the ADAMTS17 gene.
RefSeq protein product
See the reference protein sequence for A disintegrin and metalloproteinase with thrombospondin motifs 17 isoform X2 (XP_016877463.1).

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Protein sequence from Nucleotide coding region
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Ensembl [Ensembl]
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Order ADAMTS17 cDNA clone/Protein/Antibody/RNAi [OriGene]
Order ADAMTS17 cDNA clone/Protein/Antibody/RNAi
OriGene

PREDICTED: Homo sapiens ADAM metallopeptidase with thrombospondin type 1 motif 1...
PREDICTED: Homo sapiens ADAM metallopeptidase with thrombospondin type 1 motif 17 (ADAMTS17), transcript variant X2, mRNA
gi|2217300310|ref|XM_017021974.2|

Nucleotide

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Nucleotide