Gene
GNAO1
G protein subunit alpha o1
- HGNC 4389↗(opens in a new tab)
- Ensembl gene ENSG00000087258↗(opens in a new tab)
- NCBI Gene 2775↗(opens in a new tab)
Summary
- Cytogenetic location
- 16q13
- Coordinates
- Chromosome 16: 56,191,489–56,357,444 (GRCh38)
- Exons
- 9 exons across 166 kb
- Protein
- 354 amino acids
- Also known as
- G-ALPHA-o
- MANE Select transcript
- ENST00000262493.12NM_020988.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read GNAO1, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated report relevant to this gene
Epilepsy (Full Panel)
- Epilepsy
One of 171 genes linked to it
A brain disorder characterized by episodes of abnormally increased neuronal discharge resulting in transient episodes of sensory or motor neurological dysfunction, or psychic dysfunction. These episodes may or may not be associated with loss of consciousness or convulsions.
- ClinGen rates the link definitive
- 5 GenCC submitters rate it definitive or strong
How GNAO1 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 3.2 kb of the gene's 166 kb; 1,065 of those bases code for the protein.
How a genome test reads GNAO1
41
positions in GNAO1 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 166 kb of GNAO1, introns included, not only the 3.2 kb of exons.
Genes linked to the same conditions
- AARS1alanyl-tRNA synthetase 1Shares 1 condition
- ABAT4-aminobutyrate aminotransferaseShares 1 condition
- ACTL6Bactin like 6BShares 1 condition
- ADAM22ADAM metallopeptidase domain 22Shares 1 condition
- ALDH7A1aldehyde dehydrogenase 7 family member A1Shares 1 condition
- ALG13ALG13 UDP-N-acetylglucosaminyltransferase subunitShares 1 condition
- AP3B2adaptor related protein complex 3 subunit beta 2Shares 1 condition
- ARHGEF9Cdc42 guanine nucleotide exchange factor 9Shares 1 condition
- ARV1ARV1 fatty acid homeostasis modulatorShares 1 condition
- ARXaristaless related homeoboxShares 1 condition
- ATP1A2ATPase Na+/K+ transporting subunit alpha 2Shares 1 condition
- ATP1A3ATPase Na+/K+ transporting subunit alpha 3Shares 1 condition
Traits linked to GNAO1
The Human Phenotype Ontology lists these as features of the rare conditions GNAO1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Absent speech development
- Epilepsy
- Epileptic encephalopathy
- Generalized tonic seizure
- Global developmental delay
- Inability to walk
- Intellectual disability, severe
- Focal motor seizure
Show 45 more traits
- Generalized myoclonic seizure
- Intellectual disability
- Chorea
- Degeneration of cerebrum
- Delayed CNS myelination
- Difficulty sleeping
- EEG abnormality
- EEG with burst suppression
- Focal impaired awareness seizure
- Focal tonic seizure
- Hypsarrhythmia
- Increased reflexes
- Lethargy
- Multifocal epileptiform discharges
- Underdevelopment of part of brain called corpus callosum
- Atrophy/Degeneration affecting the brainstem
- Autism spectrum disorder
- Brief seizures with staring spells
- Choreoathetosis
- Degeneration of cerebellum
- Delayed myelination
- Diffuse cerebral atrophy
- Diffuse white matter abnormalities
- Disorder of involuntary muscle movements
- Dystonia
- EEG with spike-wave complexes
- Episodic ataxia
- Febrile seizure (within the age range of 3 months to 6 years)
- Fewer and broader ridges in brain
- Generalized clonic seizure
- Grand mal seizures
- Infantile spasms
- Involuntary writhing movements in fingers, hands, toes, and feet
- Jerking
- Loss of developmental milestones
- More active than typical
- Seizure affecting one half of brain
- Self-injurious behavior
- Sudden loss of muscle tone
- Tremor
- Uni- and bilateral multifocal epileptiform discharges
- Hyperactive movements
- Involuntary movements
- Orofacial dyskinesia
- Ventriculomegaly
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). GNAO1 gene: G protein subunit alpha o1. Retrieved 17 October 2026, from https://dantelabs.com/genes/gnao1
Dante Labs. GNAO1 gene: G protein subunit alpha o1 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/gnao1
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks