Entity Details
| Primary name |
POU3F4 |
| Entity type |
gene |
| Source |
Source Link |
Details
| PrimaryID | 5456 |
| RefseqGene | NG_009936 |
| Symbol | POU3F4 |
| Name | POU class 3 homeobox 4 |
| Chromosome | X |
| Location | Xq21.1 |
| TaxID | 9606 |
| Status | live |
| SourceGenome | genomic |
| SourceOrigin | natural |
| CreationDate | 1998-08-12 |
| ModificationDate | 2021-06-11 |
GO terms
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| GO | Name |
| GO:0000785 | chromatin |
| GO:0000978 | RNA polymerase II cis-regulatory region sequence-specific DNA binding |
| GO:0000981 | DNA-binding transcription factor activity, RNA polymerase II-specific |
| GO:0003700 | DNA-binding transcription factor activity |
| GO:0005654 | nucleoplasm |
| GO:0006357 | regulation of transcription by RNA polymerase II |
| GO:0007420 | brain development |
| GO:0007605 | sensory perception of sound |
| GO:0090103 | cochlea morphogenesis |
| GO:1990837 | sequence-specific double-stranded DNA binding |
| GO:2001054 | negative regulation of mesenchymal cell apoptotic process |
Diseases
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| Disease ID | Source | Name | Description |
| 304400 | OMIM | Deafness, X-linked, 2 (DFNX2) | A form of deafness characterized by both conductive hearing loss resulting from stapes (perilymphatic gusher) fixation, and progressive sensorineural deafness. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
5 interactions