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GENATLAS PHENOTYPE
last update : 10-09-2015
Symbol XPG
Location 13q33.1
Name xeroderma pigmentosum, complementation group G
Other name(s) xeroderma pigmentosum VII
Corresponding gene ERCC5
Other symbol(s) XPGC, XP7
Main clinical features
  • with/without Cockayne syndrome, XP/CS complex
  • characterized by developmental retardation, dwarfism and severe neurologic abnormalities plus sun sensitivity and other abnormalities of XP
  • Genetic determination
    Related entries including skin cancer, severe form of cockayne with early onset
    Function/system disorder dermatology
    Type disease
    Gene product
    Name endonuclease ERCC5
    Remark(s)