|Institutional Source||Beutler Lab|
|Gene Name||POU domain, class 4, transcription factor 3|
|Synonyms||Brn3c, Brn-3.1, Brn3.1|
|Is this an essential gene?||Probably essential (E-score: 0.840)|
|Stock #||R5560 (G1)|
|Chromosomal Location||42394539-42397249 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||C to A at 42395415 bp (GRCm38)|
|Amino Acid Change||Proline to Glutamine at position 141 (P141Q)|
|Ref Sequence||ENSEMBL: ENSMUSP00000025374 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000025374]|
AA Change: P141Q
PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
AA Change: P141Q
|Coding Region Coverage||
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15. [provided by RefSeq, Mar 2009]
PHENOTYPE: Affected mice are slightly smaller than their littermates and exhibit vertical head-tossing, circling and general hyperactive behavior typical of the shaker-waltzer class of mutants. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Pou4f3||
(F):5'- CTACCATACCATGAGCAGCG -3'
(R):5'- GGGGATCTTAAGATTGGCTAAAGC -3'
(F):5'- ATACCATGAGCAGCGTGCCC -3'
(R):5'- TGACCCCCAACTTGATGCG -3'