ADAMTS5 — ADAM metallopeptidase with thrombospondin type 1 motif 5
ADAMTS5 belongs to a gene co-expression module in 2 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.
ADAMTS5's module in each cell type
| Cell type | Module | Shares the module with | |
|---|---|---|---|
| Endothelial | VEGF Tip Cell Signaling Endothelial cell development | BDKRB2, CA2, CBLB, CCND1, DGKD, ESM1, GABRD, GNAI1 +7 more | View in SCUBA |
| Pericytes | Pericyte Identity Differentiation Developmental | ARHGAP15, EPB41L2, GUCY1A1, INPP4B, LGI4, LMOD1, MAP1LC3A, NFASC +11 more | View in SCUBA |
About the gene
| Synonyms | ADAMTS11, ADMP-2 |
|---|---|
| Chromosome | 21: 26917922-26967088 |
| Predicted location | Secreted |
| Essential gene | No |
| Protein class | Cancer-related genes, Predicted secreted proteins |
| Molecular function | Hydrolase, Metalloprotease, Protease |
Function
Metalloproteinase that plays an important role in connective tissue organization, development, inflammation and cell migration. Extracellular matrix (ECM) degrading enzyme that show proteolytic activity toward the hyalectan group of chondroitin sulfate proteoglycans (CSPGs) including ACAN, VCAN, BCAN and NCAN. Cleavage within the hyalectans occurs at Glu-Xaa recognition motifs. Plays a role in embryonic development, including limb and cardiac morphogenesis, and skeletal muscle development through its VCAN remodeling properties. Cleaves VCAN in the pericellular matrix surrounding myoblasts, facilitating myoblast contact and fusion which is required for skeletal muscle development and regeneration (By similarity). Participates in development of brown adipose tissue and browning of white adipose tissue (By similarity). Plays an important role for T-lymphocyte migration from draining lymph nodes following viral infection.
Human Protein Atlas · Open Targets · UniProt
Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.