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- Table of Contents
Facts about A disintegrin and metalloproteinase with thrombospondin motifs 17.
Human | |
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Gene Name: | ADAMTS17 |
Uniprot: | Q8TE56 |
Entrez: | 170691 |
Belongs to: |
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No superfamily |
A disintegrin and metalloproteinase with thrombospondin motifs 17; a disintegrin-like and metalloprotease (reprolysin type) with thrombospondintype 1 motif, 17; ADAM metallopeptidase with thrombospondin type 1 motif, 17; ADAM-TS 17; ADAM-TS17; ADAMTS-17; EC 3.4.24; EC 3.4.24.-; EC 3.4.24.80; EC 3.4.24.82; FLJ16363; FLJ32769
Mass (kDA):
121.127 kDA
Human | |
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Location: | 15q26.3 |
Sequence: | 15; NC_000015.10 (99971437..100342924, complement) |
Isoform 1 and isoform 2 are expressed at high levels in the lung, brain, whole eye and retina. Isoform 1 shows a weaker expression in the heart, kidney and skeletal muscle. Isoform 2 shows a weaker expression in the kidney, bone marrow and skeletal muscle. Isoform 1 and isoform 2 are expressed at high levels in the fetal heart, kidney, and whole eye, whereas a weak expression is seen in the fetal liver.
Secreted, extracellular space, extracellular matrix.
PMID: 11867212 by Cal S., et al. Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains.
PMID: 19836009 by Morales J., et al. Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature.