YWHAG (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma)
2007-02-01 AffiliationIdentity
HGNC
LOCATION
7q11.23
LOCUSID
ALIAS
14-3-3GAMMA,DEE56,EIEE56,PPP1R170
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: 7532
MIM: 605356
HGNC: 12852
Ensembl: ENSG00000170027
Variants:
dbSNP: 7532
ClinVar: 7532
TCGA: ENSG00000170027
COSMIC: YWHAG
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000170027 | ENST00000307630 | P61981 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38538804 | 2024 | YWHAG promotes colorectal cancer progression by regulating the CTTN-Wnt/β-catenin signaling axis. | 0 |
| 38538804 | 2024 | YWHAG promotes colorectal cancer progression by regulating the CTTN-Wnt/β-catenin signaling axis. | 0 |
| 37759388 | 2023 | YWHAG Deficiency Disrupts the EMT-Associated Network to Induce Oxidative Cell Death and Prevent Metastasis. | 2 |
| 37759388 | 2023 | YWHAG Deficiency Disrupts the EMT-Associated Network to Induce Oxidative Cell Death and Prevent Metastasis. | 2 |
| 34915349 | 2022 | Myoclonic epilepsy of infancy related to YWHAG gene mutation: towards a better phenotypic characterization. | 0 |
| 36243722 | 2022 | A heterozygous missense variant in the YWHAG gene causing developmental and epileptic encephalopathy 56 in a Chinese family. | 0 |
| 34915349 | 2022 | Myoclonic epilepsy of infancy related to YWHAG gene mutation: towards a better phenotypic characterization. | 0 |
| 36243722 | 2022 | A heterozygous missense variant in the YWHAG gene causing developmental and epileptic encephalopathy 56 in a Chinese family. | 0 |
| 33075494 | 2021 | Human adipocyte differentiation and composition of disease-relevant lipids are regulated by miR-221-3p. | 14 |
| 33159816 | 2021 | The 14-3-3/SLP76 protein-protein interaction in T-cell receptor signalling: a structural and biophysical characterization. | 4 |
| 33349918 | 2021 | Genetic diagnosis of infantile-onset epilepsy in the clinic: Application of whole-exome sequencing following epilepsy gene panel testing. | 11 |
| 33393734 | 2021 | Epilepsy and electroencephalogram evolution in YWHAG gene mutation: A new phenotype and review of the literature. | 3 |
| 33813791 | 2021 | 14-3-3γ prevents centrosome duplication by inhibiting NPM1 function. | 1 |
| 34413451 | 2021 | 14-3-3 proteins inactivate DAPK2 by promoting its dimerization and protecting key regulatory phosphosites. | 14 |
| 34709972 | 2021 | Long non-coding RNA NORAD protects against cerebral ischemia/reperfusion injury induced brain damage, cell apoptosis, oxidative stress and inflammation by regulating miR-30a-5p/YWHAG. | 15 |
Citation
Dessen P
YWHAG (tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma)
Atlas Genet Cytogenet Oncol Haematol. 2007-02-01
Online version: http://atlasgeneticsoncology.org/gene/46119/ywhag
