ZDHHC15

zDHHC palmitoyltransferase 15
OMIM: 300576, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red ZDHHC15 in Mendeliome


Version 2.55

3 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Intellectual disability, X-linked 91, 300577
Tags
  • disputed

Red ZDHHC15 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.6

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 3 reviews X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Red
    • Literature
    • Expert list
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Intellectual disability, X-linked 91, 300577
    Tags
    • disputed

    Red ZDHHC15 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.8

    3 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Genetic Health Queensland
    Phenotypes
    • Intellectual disability, X-linked 91, 300577
    Tags
    • disputed