| Name |
|---|
LHX3 GeneLIM homeobox 3 This gene encodes a member of a large family of proteins which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene cause combined pituitary hormone deficiency 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015] |
lhx3 Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term lhx3 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
LHX3 Gene SetFrom JASPAR Predicted Transcription Factor Targets target genes of the LHX3 transcription factor predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset. |
LHX3 Gene SetFrom Pathway Commons Protein-Protein Interactions interacting proteins for LHX3 from the Pathway Commons Protein-Protein Interactions dataset. |
Lhx3 Gene SetFrom JASPAR Predicted Mouse Transcription Factor Targets 2025 target genes of the Lhx3 transcription factor predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2925 dataset. |
LHX3 Gene SetFrom CM4AI KOLF21J CRISPRi Gene Perturbation Atlas genes differentially expressed following the LHX3 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas. |