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FLASH GENE
Symbol CDSN contributors: mct - updated : 26-08-2010
HGNC name corneodesmosin
HGNC id 1802
ASSOCIATED DISORDERS
corresponding disease(s) HTSS1 , PSS
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein 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
    ANIMAL & CELL MODELS
  • 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)