Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
collagen type IX alpha 2 chain
Summary
- Gene Symbol
-
- COL9A2
- Aliases
-
- MED
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Collagen
- Deafness
- Disease variant
- Disulfide bond
- Dwarfism
- Extracellular matrix
- Hydroxylation
- Proteoglycan
- Reference proteome
- Repeat
- Signal
- Stickler syndrome
- Proteins
| UniProt | Protein Name |
|---|---|
| Q14055 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| skeletal system development |
|
|
| extracellular matrix organization |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum lumen |
|
|
| extracellular region |
|
|
| collagen-containing extracellular matrix | ||
| extracellular space | ||
| collagen type IX trimer |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein homodimerization activity | ||
| protein binding | ||
| extracellular matrix structural constituent conferring tensile strength |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0014667 | disease of metabolism | |
| DOID:0050452 | mevalonic aciduria | |
| DOID:0050635 | alternating hemiplegia of childhood | |
| DOID:0050657 | Bannayan-Riley-Ruvalcaba syndrome | |
| DOID:0050902 | medulloblastoma | |
| DOID:0060224 | atrial fibrillation | |
| DOID:0060256 | Dowling-Degos disease | |
| DOID:0060258 | reticulate acropigmentation of Kitamura | |
| DOID:0070298 | multiple epiphyseal dysplasia 2 | |
| DOID:0080001 | bone disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000175 | Cleft palate |
| HP:0000201 | Pierre-Robin sequence |
| HP:0000272 | Malar flattening |
| HP:0000331 | Short chin |
| HP:0000347 | Micrognathia |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000483 | Astigmatism |
| HP:0000518 | Cataract |
| Disease ID | Disease Name |
|---|---|
| OMIM:600204 |
|
| ORPHA:250984 |
|
| ORPHA:166002 |
|
| OMIM:614284 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 181308 | WB:WBGene00000752 | ||
| 3565413 | WB:WBGene00000708 | ||
| 102360658 | LATCH12723 | ||
| 321212 | ZFIN:ZDB-GENE-030131-9786 | DANRE15812 | |
| 108272917 | ICTPU03946 | ||
| 106588834 | SALSA96822 | ||
| 115536171 | GADMO34395 | ||
| 734362 | Xenbase:XB-GENE-1006529 | ||
| 108709589 | Xenbase:XB-GENE-17336038 | ||
| 100036633 | Xenbase:XB-GENE-1006524 |
