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Antibody detects endogenous levels of total DLX5.
This gene encodes a member of a homeobox transcription factor gene family similar 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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: distal-less homeo box 5; DLX-3; Homeobox protein DLX-3; Homeobox protein DLX-5; RDLX; split hand/foot malformation type 1 with sensorineural hearing loss
Gene Aliases: AI385752; DLX5; RDLX; SHFM1D
UniProt ID: (Human) P56178, (Rat) P50575, (Mouse) P70396
Entrez Gene ID: (Human) 1749, (Rat) 25431, (Mouse) 13395
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