| 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.