Symbol
| DLX6
| contributors: npt/mct - updated : 02-04-2019
|
HGNC name
| distal-less homeobox 6
|
HGNC id
| 2919
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
| --low
|  
|
in endometriotic lesions | tumoral
|  
|  
| --over
|  
|
in endometriod adenocarcinomas | |
Susceptibility
|
to autistic spectrum disorder (ASD) |
Variant & Polymorphism
other
| a G656A base change (R219H) associted with ASD |
|
|
Candidate gene
Marker
Therapy target
| | | |
| Dlx5/Dlx6 double mutants exhibit hindlimb ectrodactyly | |
Dlx5/6-inactivation in the mouse results in a phenotype reminiscent of NTDs characterized by open thoracic and lumbar vertebral arches and failure of epaxial muscle formation at the dorsal midline |