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: 2779
MIM: 139330
HGNC: 4393
Ensembl: ENSG00000114349
Variants:
dbSNP: 2779
ClinVar: 2779
TCGA: ENSG00000114349
COSMIC: GNAT1
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 31583501 | 2020 | Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy. | 4 |
| 31583501 | 2020 | Coexistence of GNAT1 and ABCA4 variants associated with Nougaret-type congenital stationary night blindness and childhood-onset cone-rod dystrophy. | 4 |
| 31696758 | 2019 | Novel homozygous in-frame deletion of GNAT1 gene causes golden appearance of fundus and reduced scotopic ERGs similar to that in Oguchi disease in Japanese family. | 0 |
| 31696758 | 2019 | Novel homozygous in-frame deletion of GNAT1 gene causes golden appearance of fundus and reduced scotopic ERGs similar to that in Oguchi disease in Japanese family. | 0 |
| 30051303 | 2018 | Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association. | 6 |
| 30051303 | 2018 | Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association. | 6 |
| 26472407 | 2016 | A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration. | 21 |
| 26472407 | 2016 | A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration. | 21 |
| 23292452 | 2013 | Screening of candidate tumor-suppressor genes in 3p21.3 and investigation of the methylation of gene promoters in oral squamous cell carcinoma. | 12 |
| 23292452 | 2013 | Screening of candidate tumor-suppressor genes in 3p21.3 and investigation of the methylation of gene promoters in oral squamous cell carcinoma. | 12 |
| 22190596 | 2012 | GNAT1 associated with autosomal recessive congenital stationary night blindness. | 33 |
| 22190596 | 2012 | GNAT1 associated with autosomal recessive congenital stationary night blindness. | 33 |
| 20801516 | 2011 | Simultaneous mutation detection in 90 retinal disease genes in multiple patients using a custom-designed 300-kb retinal resequencing chip. | 12 |
| 20801516 | 2011 | Simultaneous mutation detection in 90 retinal disease genes in multiple patients using a custom-designed 300-kb retinal resequencing chip. | 12 |
| 17222360 | 2007 | [Expression, loss of heterozygosity, and methylation of GNAT1 gene in nasopharyngeal carcinoma]. | 3 |
Citation
Dessen P
GNAT1 (G protein subunit alpha transducin 1)
Atlas Genet Cytogenet Oncol Haematol. 2006-10-01
Online version: http://atlasgeneticsoncology.org/gene/43281/gnat1-(g-protein-subunit-alpha-transducin-1)
