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POU4F3
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]
Protein class
Disease related genes, Human disease related genes, Transcription factors
Predicted location
Intracellular
Single cell type specificity
Not detected
Immune cell specificity
Not detected in immune cells
Cell line specificity
Not detected
Interaction
Interacts with ISL1.
Molecular function
Activator, DNA-binding
More Types Infomation
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- Species Reactivity: Human
- Application: ICC/IF, WB
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For Research Use Only. Not For Clinical Use.