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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 |
|---|---|---|---|
| 115581357 | SPAAU13082 | ||
| 115592539 | SPAAU33566 | ||
| 115619778 | STRHB08333 | ||
| 116437947 | CORMO27208 | ||
| 117031517 | RHIFE20967 | ||
| 118313409 | SCOMX32084 | ||
| 118896499 | BALMU13361 | ||
| 122205132 | PANLE26013 | ||
| 123776546 | URSAM07372 |
