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MIRAGE
calcium voltage-gated channel auxiliary subunit gamma 2
Summary
- Gene Symbol
-
- CACNG2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Calcium channel
- Disease variant
- Glycoprotein
- Intellectual disability
- Phosphoprotein
- Reference proteome
- Synaptosome
- Transmembrane helix
- Voltage-gated channel
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9Y698 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein targeting to membrane | ||
| neuromuscular junction development | ||
| transmission of nerve impulse | ||
| response to calcium ion | ||
| membrane depolarization |
GO Hierarchy
biological process
cellular process [inference]
localization [inference]
biological regulation [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane | ||
| voltage-gated calcium channel complex | ||
| cell surface | ||
| endocytic vesicle membrane | ||
| AMPA glutamate receptor complex |
| GO Term | Evidence Code | PMID |
|---|---|---|
| voltage-gated calcium channel activity | ||
| protein binding | ||
| channel regulator activity | ||
| ionotropic glutamate receptor binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- voltage-dependent calcium channel
- Functional Category
-
- E: Amino acid transport and metabolism
- Q: Secondary metabolites biosynthesis, transport and catabolism
- T: Signal transduction mechanisms
| InterPro |
|---|
| PMP-22/EMP/MP20/Claudin |
| Voltage-dependent calcium channel, gamma subunit |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070040 | autosomal dominant intellectual developmental disorder 10 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 10369 | Xenbase:XB-GENE-965516 | ||
| 12300 | Xenbase:XB-GENE-965516 | MOUSE16703 | |
| 27092 | WB:WBGene00007670 | ||
| 54376 | WB:WBGene00007670 | ||
| 54377 | WB:WBGene00007670 | ||
| 59283 | WB:WBGene00007670 | ||
| 84347 | Xenbase:XB-GENE-965516 | RATNO37172 | |
| 140725 | WB:WBGene00007670 | ||
| 286800 | BOVIN29950 | ||
| 458799 | PANTR26471 |
