×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
GeneticVariation
group
CLINVAR
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
G alpha(o) is necessary for muscarinic regulation of Ca2+ channels in mouse heart.
9050846
1997
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
Augmented glucose-induced insulin release in mice lacking G(o2), but not G(o1) or G(i) proteins.
21220323
2011
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
De Novo mutations in GNAO1, encoding a Gαo subunit of heterotrimeric G proteins, cause epileptic encephalopathy.
23993195
2013
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.
25590979
2015
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay.
25966631
2016
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
Biomarker
group
CLINGEN
Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay.
25966631
2016
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
Biomarker
group
CLINGEN
The authors report 2 cases of brothers with a severe movement disorder and hypotonia without epilepsy who have been confirmed by whole exome sequencing to have a novel mutation in GNAO1 .
26060304
2016
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
The authors report 2 cases of brothers with a severe movement disorder and hypotonia without epilepsy who have been confirmed by whole exome sequencing to have a novel mutation in GNAO1 .
26060304
2016
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
GeneticVariation
group
BEFREE
The authors report 2 cases of brothers with a severe movement disorder and hypotonia without epilepsy who have been confirmed by whole exome sequencing to have a novel mutation in GNAO1 .
26060304
2016
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy.
26485252
2015
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
Biomarker
group
CLINGEN
Patients with GNAO1 mutations can present with a severe, progressive movement disorder in the absence of epilepsy.
27068059
2016
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
Patients with GNAO1 mutations can present with a severe, progressive movement disorder in the absence of epilepsy.
27068059
2016
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
GeneticVariation
group
BEFREE
Patients with GNAO1 mutations can present with a severe, progressive movement disorder in the absence of epilepsy.
27068059
2016
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
GeneticVariation
group
BEFREE
Recurrent GNAO1 Mutations Associated With Developmental Delay and a Movement Disorder .
27625011
2016
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
Biomarker
group
CLINGEN
Recurrent GNAO1 Mutations Associated With Developmental Delay and a Movement Disorder .
27625011
2016
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
GeneticVariation
group
BEFREE
A case of severe movement disorder with GNAO1 mutation responsive to topiramate.
27916449
2017
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
GeneticVariation
group
BEFREE
GNAO1 -associated epileptic encephalopathy and movement disorders : c.607G>A variant represents a probable mutation hotspot with a distinct phenotype.
28202424
2017
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome.
28357411
2017
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
Biomarker
group
CLINGEN
GNAO1 encephalopathy: Broadening the phenotype and evaluating treatment and outcome.
28357411
2017
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
Clinical Phenotype of De Novo GNAO1 Mutation: Case Report and Review of Literature.
28503590
2019
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
CausalMutation
group
CLINVAR
Movement disorder in GNAO1 encephalopathy associated with gain-of-function mutations.
28747448
2017
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
GeneticVariation
group
BEFREE
Here we review a mechanistic model in which loss-of-function (LOF) GNAO1 alleles cause epilepsy and gain-of-function (GOF) alleles are primarily associated with movement disorders .
29758257
2018
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
Biomarker
group
CLINGEN
A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features.
29935962
2018
×
Entrez Id:
2775
Gene Symbol:
GNAO1
GNAO1
0.500
Biomarker
group
BEFREE
GNAO1 has been recently identified to be involved in the pathogenesis of early infantile epileptic encephalopathy and movement disorders .
30103967
2018