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MIRAGE
potassium voltage-gated channel subfamily C member 1
Summary
- Gene Symbol
-
- KCNC1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Cell membrane
- Cell projection
- Disease variant
- Epilepsy
- Glycoprotein
- Neurodegeneration
- Phosphoprotein
- Potassium channel
- Reference proteome
- Synapse
- Transmembrane helix
- Voltage-gated channel
- Proteins
| UniProt | Protein Name |
|---|---|
| P48547 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| action potential | ||
| potassium ion transport | ||
| response to toxic substance | ||
| response to light intensity | ||
| response to auditory stimulus |
GO Hierarchy
biological process
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane | ||
| voltage-gated potassium channel complex | ||
| voltage-gated potassium channel complex | ||
| voltage-gated potassium channel complex | ||
| cell surface |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| voltage-gated potassium channel activity | ||
| delayed rectifier potassium channel activity | ||
| delayed rectifier potassium channel activity | ||
| protein binding | ||
| kinesin binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- 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:0111447 | progressive myoclonus epilepsy 7 |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 3746 | Xenbase:XB-GENE-996920 | ||
| 3747 | FB:FBgn0003386 | ||
| 3748 | FB:FBgn0003386 | ||
| 3749 | FB:FBgn0003386 | ||
| 16502 | Xenbase:XB-GENE-996920 | MOUSE55737 | |
| 16504 | FB:FBgn0003386 | ||
| 25327 | Xenbase:XB-GENE-996920 | RATNO18543 | |
| 33599 | Xenbase:XB-GENE-996920 | ||
| 99738 | FB:FBgn0003386 | ||
| 246153 | FB:FBgn0003386 |
