Col9a3 Gene Summary [Rat]
Predicted to enable protein homodimerization activity. Predicted to be an extracellular matrix structural constituent conferring tensile strength. Predicted to be involved in extracellular matrix organization. Predicted to be part of collagen type IX trimer. Predicted to be active in basement membrane and extracellular space. Human ortholog(s) of this gene implicated in Stickler syndrome; multiple epiphyseal dysplasia 3; and osteochondrodysplasia. Orthologous to human COL9A3 (collagen type IX alpha 3 chain). [provided by Alliance of Genome Resources, Apr 2025]
Details
| Type | Protein Coding |
| Official Symbol | Col9a3 |
| Official Name | collagen type IX alpha 3 chain [Source:RGD Symbol;Acc:1310255] |
| Ensembl ID | ENSRNOG00000009531 |
| Bio databases IDs | |
| Aliases | collagen type IX alpha 3 chain |
| Synonyms | collagen, type IX, alpha 3, collagen type IX alpha 3 chain, collagen, type IX, α 3, collagen type IX α 3 chain, DJ885L7.4.1, EDM3, IDD, MED, STL6 |
| Species | Rat, Rattus norvegicus |
| Orthologies |
Protein Domains
A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in rat Col9a3 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- protein homodimerization
- Collagen triple helix repeat (20 copies)
Pathways
Biological processes and signaling networks where the Col9a3 gene in rat plays a role, providing insight into its function and relevance in health or disease.
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- Dupuytren contracture
- stickler syndrome type vi
- metastasis
- hereditary arthro-ophthalmopathy
- multiple epiphyseal dysplasia 3
- Peyronie disease
- hereditary disorder
- burn
- susceptibility to intervertebral disc disease
- Ullrich congenital muscular dystrophy
role in cell
- migration
- invasion by
- epithelial-mesenchymal transition
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Extracellular Space
- endoplasmic reticulum lumen
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the rat Col9a3 gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- extracellular matrix organization
Cellular Component
Where in the cell the gene product is active
- endoplasmic reticulum lumen
- extracellular space
- collagen type IX
- extracellular region
Molecular Function
What the gene product does at the molecular level
- protein homodimerization activity
- extracellular matrix structural constituent conferring tensile strength