Symbol
| CDSN
| contributors: mct - updated : 26-08-2010
|
HGNC name
| corneodesmosin
|
HGNC id
| 1802
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
| --other
|  
|
reduced degradation of all corneodesmosomal proteins in psoriatic lesions which probably reflects the persistence of corneodesmosomes (Simon 2008) | |
Susceptibility
|
psoriasis (PSORS1) |
Variant & Polymorphism
other
| allele 971T confering psoriasis susceptibility |
|
rare allele (+1243) |
|
|
Candidate gene
Marker
Therapy target
| | | |
| Cdsn-deficient mouse skin showed detachment of the stratum corneum from the underlying granular layer and/or detachment within the upper granular layers due to the disrupted integrity of the corneodesmosomes (Matsumoto 2008) |