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MIRAGE
ADAM metallopeptidase with thrombospondin type 1 motif 17
Summary
- Gene Symbol
-
- ADAMTS17
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Calcium
- Cleavage on pair of basic residues
- Deafness
- Disulfide bond
- Dwarfism
- Extracellular matrix
- Glycoprotein
- Metal-binding
- Metalloprotease
- Proteomics identification
- Reference proteome
- Repeat
- Signal
- Zinc
- Zymogen
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| proteolysis | ||
| extracellular matrix organization |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular region | ||
| extracellular matrix |
| GO Term | Evidence Code | PMID |
|---|---|---|
| metalloendopeptidase activity | ||
| metal ion binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- thrombospondin
- Functional Category
-
- T: Signal transduction mechanisms
- X: Mobilome: prophages, transposons
| Gene Ontology |
|---|
| extracellular matrix organization |
| metal ion binding |
| metalloendopeptidase activity |
| metallopeptidase activity |
| proteolysis |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050475 | Weill-Marchesani syndrome |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 11173 | FB:FBgn0029791 | ||
| 81792 | FB:FBgn0029791 | ||
| 108153 | FB:FBgn0029791 | ||
| 170691 | Xenbase:XB-GENE-6460749 | ||
| 170692 | FB:FBgn0029791 | ||
| 171019 | FB:FBgn0029791 | ||
| 181022 | RGD:1308783 | ||
| 208936 | FB:FBgn0029791 | ||
| 233332 | MOUSE52304 | ||
| 239337 | FB:FBgn0029791 |
