STRADA

STE20-related kinase adaptor alpha
OMIM: 608626, Gene2Phenotype

10 panels

Panel Reviews Mode of inheritance Details
10 panels

Amber STRADA in Tuberous Sclerosis_Focal Cortical Dysplasia_Hemimegalencephaly


Level 2: Neurology and neurodevelopmental disorders
Version 0.48

Component of the following Super Panels:

  • Malformations of cortical development_Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Brain Malformations Flagship
    Phenotypes
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy (MIM#611087)

    Green STRADA in Hydrocephalus_Ventriculomegaly


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.123

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

    Green STRADA in Macrocephaly_Megalencephaly


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 0.140

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

    Green STRADA in Mendeliome


    Version 1.1891

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy, OMIM:611087
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy, MONDO:0012611

    Green STRADA in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.33

    Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy, OMIM:611087
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy, MONDO:0012611

    Green STRADA in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy, MIM# 611087

    Green STRADA in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy, 611087 (3), Autosomal recessive

    Green STRADA in Fetal anomalies


    Version 1.255

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Expert list
    Phenotypes
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy, OMIM:611087
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy, MONDO:0012611

    Green STRADA in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy, 611087 (3), Autosomal recessive

    Green STRADA in Renal Tubulopathies and related disorders


    Level 2: Renal and urinary tract disorders
    Version 1.14

    Component of the following Super Panels:

  • Kidneyome_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Literature
    Phenotypes
    • Polyhydramnios, megalencephaly, and symptomatic epilepsy
    • OMIM #611087