ADAMTS15 (ADAM metallopeptidase with thrombospondin type 1 motif 15)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 170689 |
| Gene name | ADAM metallopeptidase with thrombospondin type 1 motif 15 |
| Gene symbol | ADAMTS15 |
| Synonyms (NCBI Gene) |
DA12
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| Chromosome | 11 |
| Chromosome location | 11q24.3 |
| Summary | This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. ADAMTS family members share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegri |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q8TE58 | ||||||||||||||||||||||||||||||||||||||||
| Protein name | A disintegrin and metalloproteinase with thrombospondin motifs 15 (ADAM-TS 15) (ADAM-TS15) (ADAMTS-15) (EC 3.4.24.-) | ||||||||||||||||||||||||||||||||||||||||
| Protein function | Metalloprotease which has proteolytic activity against the proteoglycan VCAN, cleaving it at the 'Glu-1428-|-1429-Ala' site. Cleaves VCAN in the pericellular matrix surrounding myoblasts, facilitating myoblast contact and fusion which is require | ||||||||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in fetal liver and kidney, but not in any of the adult tissues examined. {ECO:0000269|PubMed:11867212}. | ||||||||||||||||||||||||||||||||||||||||
| Sequence |
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| Sequence length | 950 | ||||||||||||||||||||||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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