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DLX5

DLX5
Protein DLX5 PDB 2djn.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases DLX5, SHFM1D, AI385752, distal-less homeobox 5
External IDs MGI: 101926 HomoloGene: 3825 GeneCards: DLX5
Gene location (Human)
Chromosome 7 (human)
Chr. Chromosome 7 (human)
Chromosome 7 (human)
Genomic location for DLX5
Genomic location for DLX5
Band 7q21.3 Start 97,020,392 bp
End 97,025,097 bp
RNA expression pattern
PBB GE DLX5 213707 s at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005221

NM_010056
NM_198854

RefSeq (protein)

NP_005212

NP_034186
NP_942151

Location (UCSC) Chr 7: 97.02 – 97.03 Mb Chr 7: 6.88 – 6.88 Mb
PubMed search

2DJN, 4RDU

NM_005221

NM_010056
NM_198854

NP_005212

NP_034186
NP_942151

Homeobox protein DLX-5 is a protein that in humans is encoded by the distal-less homeobox 5 gene, or DLX5 gene. DLX5 is a member of DLX gene family.

This gene encodes a member of a homeobox transcription factor gene family similar to the Drosophila distal-less (Dll) gene. The encoded protein may play a role in bone development and fracture healing. Current research holds that the homeobox gene family is important in appendage development. DLX5 and DLX6 can be seen to work in conjunction and are both necessary for proper craniofacial, axial, and appendicular skeleton development. 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.


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Wikipedia

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