| GNAO1 |
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| Identifiers |
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| Aliases | GNAO1, EIEE17, G-ALPHA-o, GNAO, G protein subunit alpha o1, HLA-DQB1, NEDIM, DEE17, HG1G |
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| External IDs | OMIM: 139311; MGI: 95775; HomoloGene: 39203; GeneCards: GNAO1; OMA:GNAO1 - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 8 (mouse) |
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| | Band | 8 C5|8 45.94 cM | Start | 94,536,594 bp |
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| End | 94,696,016 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - superficial temporal artery
- entorhinal cortex
- superior frontal gyrus
- prefrontal cortex
- right frontal lobe
- putamen
- postcentral gyrus
- buccal mucosa cell
- caudate nucleus
- primary visual cortex
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| | Top expressed in | - perirhinal cortex
- entorhinal cortex
- CA3 field
- superior frontal gyrus
- primary visual cortex
- dentate gyrus of hippocampal formation granule cell
- habenula
- cerebellar cortex
- neural layer of retina
- subiculum
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| | More reference expression data |
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| BioGPS | |
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| Wikidata |
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Guanine nucleotide-binding protein G(o) subunit alpha is a protein that in humans is encoded by the GNAO1 gene.
Mutations in this gene have been shown to cause epileptic encephalopathy.