Not to be confused with
KV-1.
| KCNA1 |
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| Identifiers |
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| Aliases | KCNA1, AEMK, EA1, HBK1, HUK1, KV1.1, MBK1, MK1, RBK1, potassium voltage-gated channel subfamily A member 1 |
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| External IDs | OMIM: 176260; MGI: 96654; HomoloGene: 183; GeneCards: KCNA1; OMA:KCNA1 - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 6 (mouse) |
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| | Band | 6 F3|6 61.57 cM | Start | 126,617,360 bp |
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| End | 126,623,347 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - endothelial cell
- Brodmann area 23
- middle temporal gyrus
- cerebellar hemisphere
- primary visual cortex
- right hemisphere of cerebellum
- lateral nuclear group of thalamus
- postcentral gyrus
- putamen
- caudate nucleus
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| | Top expressed in | - sciatic nerve
- pontine nuclei
- deep cerebellar nuclei
- lateral geniculate nucleus
- medulla oblongata
- medial vestibular nucleus
- lobe of cerebellum
- cerebellar vermis
- olfactory tubercle
- inferior colliculi
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| | More reference expression data |
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| BioGPS | |
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| Wikidata |
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Potassium voltage-gated channel subfamily A member 1 also known as Kv1.1 is a shaker related voltage-gated potassium channel that in humans is encoded by the KCNA1 gene. Isaacs syndrome is a result of an autoimmune reaction against the Kv1.1 ion channel.