GO curators for mouse genes have assigned the following annotations to the gene product of Dlx5. (This text reflects annotations as of Wednesday, January 23, 2013.) Summary from NCBI RefSeq
[Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation. [provided by RefSeq, Jul 2008]Summary text based on GO annotations supported by experimental evidence in mouse
Researchers have inferred from direct assay, that the gene product of Dlx5
participates in the following biological processes:
The gene product of Dlx5 has been shown to bind to the gene products of Maged1. [6] Researchers have inferred, based on physical interactions, that the gene product of Dlx5
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Zhu H et al. (2009) Dlx5 Is a cell autonomous regulator of chondrocyte hypertrophy in mice and functionally substitutes for Dlx6 during endochondral ossification. PLoS One, 4:e8097. (PubMed:19956613)