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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:3669 | intermittent claudication | |
| DOID:3683 | lung benign neoplasm | |
| DOID:3770 | pulmonary fibrosis | |
| DOID:3772 | intraventricular meningioma | |
| DOID:381 | arthropathy | |
| DOID:3829 | pituitary adenoma | |
| DOID:3861 | medullomyoblastoma | |
| DOID:3868 | melanotic medulloblastoma | |
| DOID:3869 | childhood medulloblastoma | |
| DOID:3896 | hidradenoma |
- 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 |
|---|---|---|---|
| 397328 | PIGXX19385 | ||
| 100514895 | PIGXX19385 | ||
| 282662 | BOVIN33927 | ||
| 102168630 | CAPHI27010 | ||
| 100294605 | SHEEP17029 | ||
| 100008666 | RABIT01778 | ||
| 100766891 | CRIGR12399 | ||
| 13003 | MGI:102889 | MOUSE11620 | |
| 114122 | RGD:619940 | RATNO23452 | |
| 103677141 | URSMA29559 |
