PanelApp (test)
  1. Genes and Genomic Entities
  2. FOXG1:Ensemblv90

FOXG1:Ensemblv90

forkhead box G1
OMIM: 164874, ClinGen, DECIPHER

20 panels

Panel Reviews Mode of inheritance Details
20 panels

Green FOXG1 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.44

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions
  • Tremors_Superpanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Rett syndrome, congenital variant, MIM# 613454
    • Developmental and Epileptic Encephalopathy
    • Dystonia,
    • Athetosis
    • Parkinsonism
    • Stereotypies

    Green FOXG1 in Angelman Rett like syndromes


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.14

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Rett syndrome, congenital variant, MIM# 613454

    Green FOXG1 in Cerebral Palsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.405

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Cerebral Palsy
    • Rett syndrome, congenital variant MIM# 613454

    Green FOXG1 in Mendeliome


    Version 1.3802

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Rett syndrome, congenital variant, MIM# 613454

    Green FOXG1 in Microcephaly


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.376

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Rett syndrome, congenital variant, MIM# 613454

    Green FOXG1 in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.309

    Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • Rett syndrome, congenital variant, MIM# 613454

    Green FOXG1 in Callosome


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.578

    		0 reviews Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green FOXG1 in Regression


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.601

    		0 reviews Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green FOXG1 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.508

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • FOXG1 disorder MONDO:0100040

    Green FOXG1 in Dystonia - complex


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.290

    Component of the following Super Panels:

  • Dystonia_Superpanel
  • Progressive Neurological Conditions
  • Tremors_Superpanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Rett syndrome, congenital variant
    • Dystonia

    Red FOXG1 in Hereditary Spastic Paraplegia


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.130

    Component of the following Super Panels:

  • Hereditary Spastic Paraplegia Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • Royal Melbourne Hospital
    Phenotypes
    • Rett syndrome

    Green FOXG1 in Fetal anomalies


    Version 1.482

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Rett Syndrome, congenital variant OMIM:613454
    • Rett syndrome, congenital variant MONDO:0013270

    Green FOXG1 in Early-onset Parkinson disease


    Level 2: Neurology and neurodevelopmental disorders
    Version 3.0

    		1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Literature
    • Expert Review Green
    Phenotypes
    • Rett syndrome, congenital variant, MIM# 613454
    • Developmental and Epileptic Encephalopathy
    • Dystonia,
    • Athetosis
    • Parkinsonism
    • Stereotypies

    Green FOXG1 in Angelman Rett like syndromes


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 2.0

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green
    Phenotypes
    • Rett syndrome, congenital variant, MIM# 613454

    Green FOXG1 in Cerebral Palsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.0

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert list
    • Expert Review Green
    Phenotypes
    • Cerebral Palsy
    • Rett syndrome, congenital variant MIM# 613454

    Green FOXG1 in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.0

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Australian Genomics Health Alliance Epilepsy Flagship
    • Victorian Clinical Genetics Services
    • Expert Review Green
    Phenotypes
    • Rett syndrome, congenital variant, MIM# 613454

    Green FOXG1 in Callosome


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.0

    		0 reviews Unknown
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services

    Green FOXG1 in Regression


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.0

    		0 reviews Unknown
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services

    Green FOXG1 in Dystonia - complex


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.0

    		1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Royal Melbourne Hospital
    • Expert Review Green
    Phenotypes
    • Rett syndrome, congenital variant
    • Dystonia

    Red FOXG1 in Hereditary Spastic Paraplegia


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.0

    		1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Royal Melbourne Hospital
    • Expert Review Red
    Phenotypes
    • Rett syndrome