GATA1

GATA binding protein 1
OMIM: 305371, Gene2Phenotype

15 panels

Panel Reviews Mode of inheritance Details
15 panels

Green GATA1 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.52

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Thrombocytopenia, X-linked, with or without dyserythropoietic anemia, MIM# 300367

Green GATA1 in Bone Marrow Failure


Level 2: Haematological disorders
Version 1.112

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • Thrombocytopaenia, X-linked, with or without dyserythropoietic anaemia, MIM# 300367

    Green GATA1 in Diamond Blackfan anaemia


    Level 2: Haematological disorders
    Version 1.8

    review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Diamond-Blackfan anemia (MONDO:0015253)

    Green GATA1 in Hydrops fetalis


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 0.324

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, MIM#300835

    Green GATA1 in Mendeliome


    Version 1.2302

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Thrombocytopaenia, X-linked, with or without dyserythropoietic anaemia, MIM# 300367
    • Haemolytic anaemia due to elevated adenosine deaminase, MIM# 301083
    • Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, MIM# 300835
    • Diamond-Blackfan anemia (MONDO:0015253)

    Amber GATA1 in Photosensitivity Syndromes


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.8

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Erythropoietic porphyria

    Red GATA1 in Radial Ray Abnormalities


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.15

    Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel
  • review Unknown
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services

    Red GATA1 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.63

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Genetic Health Queensland

    Amber GATA1 in Haem degradation and bilirubin metabolism defects


    Level 2: Metabolic disorders
    Version 0.17

    Component of the following Super Panels:

  • Liverome Superpanel
  • Metabolic Disorders Superpanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Amber
    • Royal Melbourne Hospital
    Phenotypes
    • Thrombocytopenia, X-linked, with or without dyserythropoietic anemia, 300367
    • Congenital erythropoietic porphyria

    Red GATA1 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    • BabySeq Category A gene
    Phenotypes
    • Porphyria, congenital erythropoietic
    • Dyserythropoietic anemia with thrombocytopenia

    Green GATA1 in Red cell disorders


    Level 2: Haematological disorders
    Version 1.29

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Yorkshire and North East GLH
    • NHS GMS
    • Wessex and West Midlands GLH
    • North West GLH
    • London South GLH
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • Thrombocytopenia, X-linked, with or without dyserythropoietic anaemia, MIM# 300367
    • Haemolytic anaemia due to elevated adenosine deaminase, MIM# 301083

    Green GATA1 in Fetal anomalies


    Version 1.313

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Expert list
    • Expert Review Green
    • Expert list
    Phenotypes
    • Anaemia, X-linked, with/without neutropaenia and/or platelet abnormalities, MIM#300835

    Green GATA1 in IBMDx study


    Version 0.33

    review Unknown
    Sources
    • Expert Review Green
    • IBMDx Study
    • Expert Review Green
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • Thrombocytopaenia, X-linked, with or without dyserythropoietic anaemia, MIM# 300367

    Red GATA1 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.116

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • BabySeq Category C gene
    • BabySeq Category A gene
    • Expert Review Red
    • BeginNGS
    Phenotypes
    • Blackfan-Diamond anaemia, ORPHA:124
    • Congenital erythropoietic porphyria, ORPHA:79277
    • Porphyria, congenital erythropoietic
    • Dyserythropoietic anemia with thrombocytopenia
    • Anaemia, X-linked, with/without neutropenia and/or platelet abnormalities, MIM# 300835
    • Thrombocytopenia, X-linked, with or without dyserythropoietic anaemia, MIM# 300367

    Green GATA1 in Transplant Co-Morbidity Superpanel


    Level 2: Screening
    Version 0.18

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert list
    • Expert Review Green
    Phenotypes
    • Thrombocytopenia, X-linked, with or without dyserythropoietic anemia, MIM# 300367