| Gene Symbol | DLX5 |
| Entrez Gene ID | 1749 |
| Full Name | distal-less homeobox 5 |
| Synonyms | SHFM1D |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | 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]. |
| Disorder MIM: | |
| Disorder Html: | ?Split-hand/foot malformation 1 with sensorineural hearing loss, 220600 (3) |









































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