Harmonizome 3.0

POU class 4 homeobox 3

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]

RBM27-POU4F3 readthrough

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term pou4f3 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From JASPAR Predicted Human Transcription Factor Targets 2025

target genes of the POU4F3 transcription factor predicted using known transcription factor binding site motifs from the JASPAR Predicted Human Transcription Factor Targets dataset.

From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas

genes differentially expressed following the POU4F3 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.

From PerturbAtlas Signatures of Differentially Expressed Genes for Mouse Gene Perturbations

genes differentially expressed following the Perturb_4843_OE_Gfi1/Pou4f3/Atoh1_SRP220284 gene perturbation from the PerturbAtlas Signatures of Differentially Expressed Genes for Gene Perturbations dataset.