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  Domain Name: DEXDc
DEAD-like helicases superfamily.
No pairwise interactions found for the domain DEXDc

Total Mutations Found: 80
Total Disease Mutations Found: 25
This domain occurred 108 times on human genes (196 proteins).



  ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED
  BREAST CANCER, INVASIVE DUCTAL
  CEREBROOCULOFACIOSKELETAL SYNDROME 1
  CHARGE SYNDROME
  COCKAYNE SYNDROME B
  COLON CANCER, SOMATIC
  DISTAL SPINAL MUSCULAR ATROPHY, AUTOSOMAL RECESSIVE, 1
  EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET
  MENTAL RETARDATION, AUTOSOMAL DOMINANT 16
  NICOLAIDES-BARAITSER SYNDROME
  OROFACIODIGITAL SYNDROME V
  PLEUROPULMONARY BLASTOMA (PPB)
  SCHIMKE IMMUNOOSSEOUS DYSPLASIA
  TRICHOHEPATOENTERIC SYNDROME 2
  XERODERMA PIGMENTOSUM B/COCKAYNE SYNDROME


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for DEXDc






































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Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.

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