Name

HMX2 Gene

H6 family homeobox 2

The protein encoded by this gene is a member of the NKL homeobox family of transcription factors. Members in this family are of ancient origin and play an important role in organ development during embryogenesis. A related mouse protein plays a role in patterning of inner ear structures. In humans, variations in a region containing this gene have been associated with inner ear malformations, vestibular dysfunction, and hearing loss. [provided by RefSeq, Aug 2012]

hmx2 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term hmx2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

HMX2 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for HMX2 from the Pathway Commons Protein-Protein Interactions dataset.

Hmx2 Gene Set

From JASPAR Predicted Mouse Transcription Factor Targets 2025

target genes of the Hmx2 transcription factor predicted using known transcription factor binding site motifs from the JASPAR Predicted Mouse Transcription Factor Targets 2925 dataset.

HMX2 Gene Set

From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas

genes differentially expressed following the HMX2 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.