Identity
HGNC
LOCATION
16q13
LOCUSID
ALIAS
DEE17,EIEE17,G-ALPHA-o,GNAO,HLA-DQB1,NEDIM
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 2775
MIM: 139311
HGNC: 4389
Ensembl: ENSG00000087258
Variants:
dbSNP: 2775
ClinVar: 2775
TCGA: ENSG00000087258
COSMIC: GNAO1
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36980817 | 2023 | Visual Function in Children with GNAO1-Related Encephalopathy. | 1 |
| 37034444 | 2023 | Dystonic Cerebral Palsy Phenotype Due to GNAO1 Variant Responsive to Levodopa. | 1 |
| 37225406 | 2023 | Genotype-phenotype correlation and treatment effects in young patients with GNAO1-associated disorders. | 4 |
| 37887313 | 2023 | Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing GNAO1 Mutation P170R. | 0 |
| 36980817 | 2023 | Visual Function in Children with GNAO1-Related Encephalopathy. | 1 |
| 37034444 | 2023 | Dystonic Cerebral Palsy Phenotype Due to GNAO1 Variant Responsive to Levodopa. | 1 |
| 37225406 | 2023 | Genotype-phenotype correlation and treatment effects in young patients with GNAO1-associated disorders. | 4 |
| 37887313 | 2023 | Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing GNAO1 Mutation P170R. | 0 |
| 35292727 | 2022 | G0S2 regulates innate immunity in Kawasaki disease via lncRNA HSD11B1-AS1. | 4 |
| 35722775 | 2022 | Highlighting the Dystonic Phenotype Related to GNAO1. | 9 |
| 35292727 | 2022 | G0S2 regulates innate immunity in Kawasaki disease via lncRNA HSD11B1-AS1. | 4 |
| 35722775 | 2022 | Highlighting the Dystonic Phenotype Related to GNAO1. | 9 |
| 32898863 | 2021 | Identification of functional cooperative mutations of GNAO1 in human acute lymphoblastic leukemia. | 10 |
| 33408414 | 2021 | Structures of the glucocorticoid-bound adhesion receptor GPR97-G(o) complex. | 51 |
| 33442900 | 2021 | Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype. | 3 |
Citation
Dessen P
GNAO1 (G protein subunit alpha o1)
Atlas Genet Cytogenet Oncol Haematol. 2006-10-01
Online version: http://atlasgeneticsoncology.org/gene/43279/gnao1-(g-protein-subunit-alpha-o1)
