Gene entry
GNAO1
G protein subunit alpha o1
- Chromosome
- 16
- Cytoband
- 16q13
- Variants (rsID)
- 49
GNAO1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q13). Its official name is “G protein subunit alpha o1”. The reference table lists 49 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs200127285Likely benignsingle nucleotide variantEarly infantile epileptic encephalopathy with suppression bursts
- rs886039494Pathogenicsingle nucleotide variantNeurodevelopmental disorder with involuntary movements|Early infantile epileptic encephalopathy with suppression bursts|Inborn genetic diseases|Movement disorder|Developmental and epileptic encephalopathy, 17
- rs886041715Pathogenicsingle nucleotide variantEarly infantile epileptic encephalopathy with suppression bursts
Other listed variants
- rs899228
- rs899239
- rs922445
- rs1190762
- rs1993886
- rs2126986
- rs2241952
- rs2587885
- rs2587891
- rs3790096
- rs3811360
- rs4783937
- rs4784651
- rs7185805
- rs7206796
- rs9927506
- rs11640074
- rs12600108
- rs12920828
- rs12930151
- rs13337678
- rs17282194
- rs62036910
- rs62038122
- rs72814453
- rs72814456
- rs74246242
- rs75755709
- rs76402914
- rs77123123
- rs78005998
- rs79244912
- rs80322217
- rs112686726
- rs113140045
- rs117182053
- rs117501040
- rs117531690
- rs117864941
- rs118114500
- rs118189490
- rs138086751
- rs141980827
- rs142606472
- rs375704187
- rs587777057
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.