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: 2070
MIM: 603550
HGNC: 3522
Ensembl: ENSG00000112319
Variants:
dbSNP: 2070
ClinVar: 2070
TCGA: ENSG00000112319
COSMIC: EYA4
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37777742 | 2023 | EYA4 promotes breast cancer progression and metastasis through its role in replication stress avoidance. | 2 |
| 37777742 | 2023 | EYA4 promotes breast cancer progression and metastasis through its role in replication stress avoidance. | 2 |
| 35578334 | 2022 | Identification of a novel CNV at the EYA4 gene in a Chinese family with autosomal dominant nonsyndromic hearing loss. | 2 |
| 36453428 | 2022 | Aberrant DNA methylation and expression of EYA4 in gastric cardia intestinal metaplasia. | 0 |
| 35578334 | 2022 | Identification of a novel CNV at the EYA4 gene in a Chinese family with autosomal dominant nonsyndromic hearing loss. | 2 |
| 36453428 | 2022 | Aberrant DNA methylation and expression of EYA4 in gastric cardia intestinal metaplasia. | 0 |
| 33301229 | 2021 | Early truncation of the N-terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype. | 5 |
| 33631386 | 2021 | Prognostic Role of EYA4 in Lower Grade Glioma with IDH1 Mutation and 1p19q Co-Deletion. | 4 |
| 33745059 | 2021 | Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults. | 6 |
| 33859130 | 2021 | Identification of a Novel Copy Number Variation of EYA4 Causing Autosomal Dominant Non-syndromic Hearing Loss. | 3 |
| 33301229 | 2021 | Early truncation of the N-terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype. | 5 |
| 33631386 | 2021 | Prognostic Role of EYA4 in Lower Grade Glioma with IDH1 Mutation and 1p19q Co-Deletion. | 4 |
| 33745059 | 2021 | Genome-first approach to rare EYA4 variants and cardio-auditory phenotypes in adults. | 6 |
| 33859130 | 2021 | Identification of a Novel Copy Number Variation of EYA4 Causing Autosomal Dominant Non-syndromic Hearing Loss. | 3 |
| 32107406 | 2020 | Prevalence and clinical features of hearing loss caused by EYA4 variants. | 15 |
Citation
Dessen P
EYA4 (EYA transcriptional coactivator and phosphatase 4)
Atlas Genet Cytogenet Oncol Haematol. 2009-09-01
Online version: http://atlasgeneticsoncology.org/gene/51134/eya4-(eya-transcriptional-coactivator-and-phosphatase-4)
