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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Dystroglycan
Summary
- Gene Symbol
-
- Dg
- Organism
- Drosophila melanogaster (fruit fly)
Annotation
- Keyword
-
- Cytoskeleton
- Nucleus
- Phosphoprotein
- Postsynaptic cell membrane
- Proteomics identification
- Reference proteome
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A0C4DHF6 |
|
| Q8WR08 |
|
| A1ZA89 |
|
| Q8STB9 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| oocyte axis specification | ||
| oocyte anterior/posterior axis specification | ||
| establishment or maintenance of apical/basal cell polarity | ||
| establishment of cell polarity | ||
| establishment or maintenance of polarity of follicular epithelium |
GO Hierarchy
biological process
cellular process [inference]
biological regulation [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| laminin receptor activity | ||
| calcium ion binding | ||
| laminin binding | ||
| structural constituent of muscle |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- uncharacterized protein
- Functional Category
-
- E: Amino acid transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| calcium ion binding |
| morphogenesis of an epithelium |
| muscle attachment |
| nerve development |
Alliance of Genome Resources
- Expression
| Location | References |
|---|---|
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050453 | lissencephaly | |
| DOID:0050559 | Fukuyama congenital muscular dystrophy | |
| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
| DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | |
| DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P | |
| DOID:0111232 | congenital muscular dystrophy-dystroglycanopathy type A9 | |
| DOID:0112374 | muscular dystrophy-dystroglycanopathy | |
| DOID:11650 | bronchopulmonary dysplasia | |
| DOID:11723 | Duchenne muscular dystrophy | |
| DOID:12236 | primary biliary cholangitis |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 1605 | HGNC:2666 | |||
| 13138 | MGI:101864 | |||
| 114489 | RGD:621890 | |||
| 186365 | WB:WBGene00018943 | |||
| 286829 | ZFIN:ZDB-GENE-021223-1 | |||
| 549272 | Xenbase:XB-GENE-1015769 | |||
| 4805356 | 7237_1:000eba | |||
| 6496411 | 7217_1:0023a9 | |||
| 6531484 | 7245_1:0018fc | |||
| 6548771 | 7220_1:002429 |
