1. Genes and Genomic Entities
  2. DLX6

DLX6

distal-less homeobox 6
OMIM: 600030, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red DLX6 in Limb disorders


Level 2: Musculoskeletal
Version 7.17
Latest signed off version: v7.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • London South East RGC GSTT
    • Viapath
    Phenotypes
    • Split hand/foot malformation 1
    Tags
    • polygenic
    Red DLX6 in Skeletal dysplasia


    Level 2: Musculoskeletal
    Version 8.33
    Latest signed off version: v8.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Paediatric disorders

    		•  review Unknown
    Sources
    • NHS GMS
    • Expert Review Red
    Phenotypes
    • Split-hand/foot malformation 1 183600
    • Split-hand/foot malformation 1 with sensorineural hearing loss 220600