ATRX

ATRX, chromatin remodeler
OMIM: 300032, Gene2Phenotype

21 panels

Panel Reviews Mode of inheritance Details
21 panels

Green ATRX in Angelman Rett like syndromes


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.10

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
  • Victorian Clinical Genetics Services
Phenotypes
  • ATR-X-related syndrome MONDO:0016980

Amber ATRX in Arthrogryposis


Level 2: Neurology and neurodevelopmental disorders
Version 0.411

Component of the following Super Panels:

  • Neuromuscular Superpanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    Phenotypes
    • Alpha-thalassemia/mental retardation syndrome, MIM# 301040

    Green ATRX 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
    • Expert Review
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Differences of Sex Development


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 0.293

    review Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green ATRX 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
    • Victorian Clinical Genetics Services
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Microcephaly


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.269

    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
    • Victorian Clinical Genetics Services
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Cancer Predisposition_Paediatric


    Level 2: Cancer
    Version 0.131

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980
    • Osteosarcoma, mild to severe intellectual disability, facial, skeletal, urogenital, and hematopoietic anomalies.

    Green ATRX 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
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Callosome


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.522

    review Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green ATRX in Homologous_recombination_deficiency_WTS_UMCCR


    Level 2: Cancer
    Version 0.43

    review Unknown
    Sources
    • Literature
    • Expert Review Green
    Tags
    • umccr

    Green ATRX 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
    • Genetic Health Queensland
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Gastrointestinal neuromuscular disease


    Level 2: Gastroenterological disorders
    Version 1.24

    Component of the following Super Panels:

  • Neuromuscular Superpanel
  • 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
    • NHS GMS
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Red cell disorders


    Level 2: Haematological disorders
    Version 1.24

    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
    • London South GLH
    • NHS GMS
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Red ATRX in Clefting disorders

    Level 3: Dysmorphic disorders
    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 0.252

    review Unknown
    Sources
    • Expert Review Red
    Phenotypes
    • MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1
    • MRXHF1

    Green ATRX in Growth failure


    Version 1.76

    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
    • Genomics England PanelApp
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Fetal anomalies


    Version 1.255

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Victorian Clinical Genetics Services
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980
    • Mental retardation-hypotonic facies syndrome, X-linked, 309580 (3)

    Red ATRX in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • BabySeq Category A gene
    Phenotypes
    • ATR-X-related syndrome MONDO:0016980

    Green ATRX in Prepair 500+


    Level 2: Screening
    Version 1.1

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Mental retardation-hypotonic facies syndrome, X-linked, 309580 (3)