YARS2

tyrosyl-tRNA synthetase 2
OMIM: 610957, Gene2Phenotype

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Green YARS2 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Myopathy, lactic acidosis, and sideroblastic anaemia 2 MIM# 613561
  • sideroblastic anaemia
  • muscle atrophy
  • myopathy
  • lactic acidosis
  • Hypertrophic cardiomyopathy
  • Hepatomegaly
  • Decreased cytochrome C oxidase activity

Green YARS2 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.927

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Mitochondrial Flagship
    Phenotypes
    • Myopathy, lactic acidosis, and sideroblastic anaemia 2 MIM# 613561
    • sideroblastic anaemia
    • muscle atrophy
    • myopathy
    • lactic acidosis
    • Hypertrophic cardiomyopathy
    • Hepatomegaly
    • Decreased cytochrome C oxidase activity

    Green YARS2 in Rhabdomyolysis and Metabolic Myopathy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.6

    Component of the following Super Panels:

  • Myopathy Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    • Expert Review Green
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • Myopathy, lactic acidosis, and sideroblastic anemia 2 MIM#613561

    Green YARS2 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
    • Myopathy, lactic acidosis, and sideroblastic anemia 2, 613561 (3)

    Red YARS2 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Myopathy, lactic acidosis, and sideroblastic anemia

    Green YARS2 in Red cell disorders


    Level 2: Haematological disorders
    Version 1.24

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Yorkshire and North East GLH
    • NHS GMS
    • Wessex and West Midlands GLH
    • North West GLH
    • London South GLH
    Phenotypes
    • Myopathy, lactic acidosis, and sideroblastic anaemia 2 MIM# 613561
    • sideroblastic anaemia
    • muscle atrophy
    • myopathy
    • lactic acidosis
    • Hypertrophic cardiomyopathy
    • Hepatomegaly
    • Decreased cytochrome C oxidase activity

    Green YARS2 in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Myopathy, lactic acidosis, and sideroblastic anemia 2, 613561 (3)

    Red YARS2 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Myopathy, lactic acidosis, and sideroblastic anemia

    Green YARS2 in Prepair 500+


    Level 2: Screening
    Version 1.1

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Myopathy, lactic acidosis, and sideroblastic anemia 2, 613561 (3)