SLITRK2

SLIT and NTRK like family member 2
OMIM: 300561, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green SLITRK2 in Cerebral Palsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.356

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Intellectual developmental disorder, X-linked MIM#301107

Green SLITRK2 in Mendeliome


Version 1.1891

review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Intellectual developmental disorder, X-linked 111, MIM# 301107

Green SLITRK2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Intellectual developmental disorder, X-linked 111, MIM# 301107

    Green SLITRK2 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Intellectual developmental disorder, X-linked 111, MIM# 301107