TMEM161B

transmembrane protein 161B
ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green TMEM161B in Polymicrogyria and Schizencephaly


Level 2: Neurology and neurodevelopmental disorders
Version 0.208

Component of the following Super Panels:

  • Malformations of cortical development_Superpanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Literature
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092, TMEM161B-related

    Green TMEM161B in Mendeliome


    Version 1.5025

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092, TMEM161B-related

    Green TMEM161B in Microcephaly


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.444

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Literature
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092, TMEM161B-related

    Green TMEM161B in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.435

    Component of the following Super Panels:

  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Literature
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092, TMEM161B-related

    Green TMEM161B in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.831

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    • Expert Review Green
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092, TMEM161B-related