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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| POU4F3-20-RE | 20 (40 μL) | 200 μL |  |
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| POU4F3-20-OR | 20 (40 μL) | 200 μL |  |
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| POU4F3-20-GO | 20 (40 μL) | 200 μL |  |
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| POU4F3-20-GR | 20 (40 μL) | 200 μL |  |
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| POU4F3-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : POU4F3
Gene Name : POU class 4 homeobox 3
Chromosome : CHR 5: 146,339,023-146,340,519
Locus : 5q32
Alt. Genes : FAM13A
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