anti-ADAMTS2 Antikörper
ADAMTS2 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family.
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anti-ADAMTS2 Antikörper (A Disintegrin-Like and Metallopeptidase (Reprolysin Type) with Thrombospondin Type 1 Motif, 2) Primary Antibody
ADAMTS2 Antigen-Profil
Protein Überblick
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. The enzyme encoded by this gene excises the N-propeptide of type I, type II and type V procollagens. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in multiple transcript variants.
Genbezeichner und Symbole assoziert mit ADAMTS2
- ADAM metallopeptidase with thrombospondin type 1 motif 2 (ADAMTS2) Antikörper
- ADAM-TS2 Antikörper
- ADAMTS-2 Antikörper
- ADAMTS-3 Antikörper
- NPI Antikörper
- PC I-NP Antikörper
- PCI-NP Antikörper
- PCINP Antikörper
- PCPNI Antikörper
- PNPI Antikörper
Bezeichner auf Proteinebene für ADAMTS2
A disintegrin and metalloproteinase with thrombospondin motifs 2 , a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 2 , procollagen I N-proteinase , procollagen I/II amino propeptide-processing enzyme , procollagen N-endopeptidase
| GENE ID | SPEZIES |
|---|---|
| 9509 | Homo sapiens |
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