PanelApp (staging)
  1. Genes and Genomic Entities
  2. FBXO11

FBXO11

F-box protein 11
OMIM: 607871, ClinGen, DECIPHER

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green FBXO11 in Craniosynostosis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.68

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • intellectual developmental disorder with dysmorphic facies and behavioral abnormalities, MIM# 618089

Green FBXO11 in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Intellectual Developmental Disorder with Dysmorphic Facies and Behavioural Abnormalities, MIM#618089

Green FBXO11 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.108

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities, 618089

    Green FBXO11 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.63

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Intellectual Developmental Disorder with Dysmorphic Facies and Behavioural Abnormalities, MIM#618089

    Amber FBXO11 in Clefting disorders

    Level 3: Dysmorphic disorders
    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 0.260

    		1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities, 618089
    • cleft lip

    Red FBXO11 in Fetal anomalies


    Version 1.313

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    Phenotypes
    • Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities, MIM# 618089