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: 5459
MIM: 602460
HGNC: 9220
Ensembl: ENSG00000091010
Variants:
dbSNP: 5459
ClinVar: 5459
TCGA: ENSG00000091010
COSMIC: POU4F3
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000091010 | ENST00000646991 | Q15319 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37072551 | 2023 | Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses. | 2 |
| 37537203 | 2023 | Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspects. | 4 |
| 37072551 | 2023 | Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses. | 2 |
| 37537203 | 2023 | Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspects. | 4 |
| 34250087 | 2021 | A Missense POU4F3 Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities. | 1 |
| 34250087 | 2021 | A Missense POU4F3 Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities. | 1 |
| 32390314 | 2020 | Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families. | 6 |
| 32684921 | 2020 | Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss. | 6 |
| 32390314 | 2020 | Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families. | 6 |
| 32684921 | 2020 | Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss. | 6 |
| 29850532 | 2018 | A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family. | 9 |
| 29850532 | 2018 | A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family. | 9 |
| 27535032 | 2017 | Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss. | 18 |
| 28545070 | 2017 | POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss. | 27 |
| 28790396 | 2017 | A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss. | 14 |
Citation
Dessen P
POU4F3 (POU class 4 homeobox 3)
Atlas Genet Cytogenet Oncol Haematol. 2007-02-01
Online version: http://atlasgeneticsoncology.org/gene/46553/pou4f3
