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MIRAGE
potassium voltage-gated channel modifier subfamily V member 2
Summary
- Gene Symbol
-
- KCNV2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Cell membrane
- Cone-rod dystrophy
- Disease variant
- Glycoprotein
- Potassium channel
- Reference proteome
- Transmembrane helix
- Voltage-gated channel
- Proteins
| UniProt | Protein Name |
|---|---|
| Q8TDN2 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| action potential | ||
| protein homooligomerization | ||
| potassium ion transmembrane transport |
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane | ||
| voltage-gated potassium channel complex | ||
| membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| voltage-gated potassium channel activity | ||
| protein binding | ||
| potassium channel regulator activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Voltage-gated potassium channel
- Functional Category
-
- E: Amino acid transport and metabolism
- J: Translation, ribosomal structure and biogenesis
- K: Transcription
- T: Signal transduction mechanisms
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0081022 | retinal cone dystrophy 3B |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 102134987 | MACFA12093 | ||
| 102177237 | CAPHI28976 | ||
| 102443330 | MYOLU08476 | ||
| 103043553 | ASTMX10028 | ||
| 103156853 | POEFO21033 | ||
| 103178094 | CALMI14624 | ||
| 103219521 | CHLSB03394 | ||
| 103251103 | CARSF23272 | ||
| 103740991 | NANGA08336 | ||
| 104682218 | RHIRO39105 |
