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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
versican
Summary
- Gene Symbol
-
- VCAN
- Aliases
-
- PG-M
- versican proteoglycan
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Calcium
- Cataract
- Cell projection
- Direct protein sequencing
- Disulfide bond
- EGF-like domain
- Extracellular matrix
- Glycoprotein
- Hyaluronic acid
- Immunoglobulin domain
- Lectin
- Phosphoprotein
- Proteoglycan
- Proteomics identification
- Reference proteome
- Repeat
- Signal
- Sushi
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| skeletal system development | ||
| osteoblast differentiation | ||
| glial cell differentiation | ||
| cell recognition |
|
|
| central nervous system development |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular matrix |
|
|
| endoplasmic reticulum lumen |
|
|
| extracellular region | ||
| photoreceptor outer segment | ||
| Golgi lumen |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular matrix structural constituent conferring compression resistance | ||
| hyaluronic acid binding | ||
| calcium ion binding | ||
| carbohydrate binding | ||
| protein binding |
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:0050156 | idiopathic pulmonary fibrosis | |
| DOID:0050387 | nonpapillary renal cell carcinoma | |
| DOID:0050469 | Costello syndrome | |
| DOID:0050589 | inflammatory bowel disease | |
| DOID:0050801 | androgenic alopecia | |
| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | |
| DOID:0050819 | obsolete Matthew-Wood syndrome | |
| DOID:0050902 | medulloblastoma | |
| DOID:0060247 | Smith-McCort dysplasia | |
| DOID:0080199 | colorectal carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000501 | Glaucoma |
| HP:0000518 | Cataract |
| HP:0000533 | Chorioretinal atrophy |
| HP:0000545 | Myopia |
| HP:0000572 | Visual loss |
| HP:0000648 | Optic atrophy |
| HP:0001123 | Visual field defect |
| HP:0007643 | Peripheral tractional retinal detachment |
| HP:0007722 | Retinal pigment epithelial atrophy |
| Disease ID | Disease Name |
|---|---|
| OMIM:143200 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 116993 | ZFIN:ZDB-GENE-011023-1 | ||
| 323465 | ZFIN:ZDB-GENE-030131-2185 | ||
| 100037127 | Xenbase:XB-GENE-922310 | ||
| 100101672 | Xenbase:XB-GENE-922302 | ||
| 101952386 | CHRPI03317 | ||
| 109308080 | CROPO12015 | ||
| 103823054 | SERCA19959 | ||
| 103109705 | ERIEU13954 | ||
| 100402664 | CALJA27407 | ||
| 105599122 | CERAT06984 |
