| Type | Description |
|---|---|
| Definition | POU domain, class 3, transcription factor 4 |
| Date | Results | Publications |
|---|---|---|
| 2015-06-20 12:51:00 | Brn4 substantially contributes to cochlear gap junction properties to maintain the proper EP in cochleae, similar to connexin-related deafness. | 25259580 |
| 2015-06-20 11:41:00 | Efnb2 expression was attenuated in Pou3f4 hemizygous null mutants relative to control. | 25299585 |
| 2014-01-25 11:59:00 | Results show three novel mutations in the POU3F4 gene resulting in profound hearing loss in both humans and mice. | 23606368 |
| 2012-03-10 10:25:00 | This study indicated a model whereby Pou3f4 in the otic mesenchyme establishes an Eph/ephrin-mediated fasciculation signal that promotes inner radial bundle formation. | 22243746 |
| 2011-07-09 11:59:00 | pou3f4 expression in inner ear might be under the control of distinct regulatory elements that fine-tune the spatio-temporal activity of this gene | 21209840 |
| Type | IDs |
|---|---|
| Synonymous | Brn-4, Brn4, OTF-9, Otf9, Slf, oct-9 |
| Gene |
UniProtKB-ID:
PO3F4_MOUSE,
A6H6L6_MOUSE
UniprotKB:
P62515,
A6H6L6
UniParc:
UPI0000025229
EMBL:
BC145919,
M88301,
BC138657
Ensembl:
ENSMUSG00000056854
KO:
mmu:18994
|
| Nucleutide sequences |
EMBL-CDS:
AAA39962.1,
AAI38658.1,
AAI45920.1
Ensembl_TRS:
ENSMUST00000078229
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000077354
RefSeq:
NP_032927.1
|
| Others |
UniRef100:
UniRef100_P62515
UniRef90:
UniRef90_P49335
UniRef50:
UniRef50_P49335
UniGene:
Mm.56946,
Mm.405149
CCDS:
CCDS30355.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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| Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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