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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
syndecan 2
Summary
- Gene Symbol
-
- SDC2
- Aliases
-
- CD362
- SYND2
- fibroglycan
- syndecan proteoglycan 2
- Organism
- Homo sapiens (human)
Annotation
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cell migration | ||
| biological_process | ||
| regulation of dendrite morphogenesis | ||
| dendrite morphogenesis |
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum lumen |
|
|
| Golgi lumen |
|
|
| cell surface | ||
| plasma membrane | ||
| collagen-containing extracellular matrix |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| PDZ domain binding | ||
| protein binding | ||
| identical protein binding |
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:0060190 | ileocolitis | |
| DOID:0060255 | rippling muscle disease 2 | |
| DOID:0060270 | pontocerebellar hypoplasia type 2D | |
| DOID:0060276 | pontocerebellar hypoplasia type 7 | |
| DOID:0060277 | pontocerebellar hypoplasia type 8 | |
| DOID:0060278 | pontocerebellar hypoplasia type 9 | |
| DOID:0060469 | Miller-Dieker lissencephaly syndrome | |
| DOID:0060807 | syndromic X-linked intellectual disability Najm type | |
| DOID:0070027 | CST3-related cerebral amyloid angiopathy | |
| DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 181259 | WB:WBGene00004749 | ||
| 37447 | FB:FBgn0010415 | ||
| 103175123 | CALMI06968 | ||
| 102346562 | LATCH07172 | ||
| 282667 | ZFIN:ZDB-GENE-021206-3 | ||
| 379912 | Xenbase:XB-GENE-6254482 | ||
| 394283 | Xenbase:XB-GENE-6254666 | ||
| 101950596 | CHRPI06138 | ||
| 113439888 | PSETE11644 | ||
| 100073947 | ORNAN20670 |
