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NR2E3 Genenuclear receptor subfamily 2, group E, member 3 This protein is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in adults. Members of this family are characterized by discrete domains that function in DNA and ligand binding. This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008] |
nr2e3 Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term nr2e3 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
NR2E3 Gene SetFrom JASPAR Predicted Transcription Factor Targets target genes of the NR2E3 transcription factor predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset. |
NR2E3 Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for NR2E3 from the Pathway Commons Protein-Protein Interactions dataset. |
Nr2e3 Gene SetFrom JASPAR Predicted Mouse Transcription Factor Targets 2025 target genes of the Nr2e3 transcription factor predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2925 dataset. |
NR2E3 Gene SetFrom CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the NR2E3 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas. |