PGK1

phosphoglycerate kinase 1
OMIM: 311800, Gene2Phenotype

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Green PGK1 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.3

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions
  • Tremors_Superpanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Phosphoglycerate kinase 1 deficiency, MIM# 300653
    • Haemolytic anaemia
    • Rhabdomyolysis
    • Myopathy
    • Juvenile Parkinsonism
    • OMIM 300653

    Green PGK1 in Glycogen Storage Diseases


    Level 2: Metabolic disorders
    Version 1.2

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Phosphoglycerate kinase 1 deficiency, MIM# 300653
    • MONDO:0010392

    Green PGK1 in Mendeliome


    Version 1.1902

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Phosphoglycerate kinase 1 deficiency, MIM# 300653
    • MONDO:0010392

    Green PGK1 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Phosphoglycerate kinase 1 deficiency, MIM# 300653
    • MONDO:0010392

    Green PGK1 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 X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Expert list
    • Royal Melbourne Hospital
    • Victorian Clinical Genetics Services
    Phenotypes
    • Phosphoglycerate kinase 1 deficiency 300653
    • MONDO:0010392

    Green PGK1 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
    • Phosphoglycerate kinase 1 deficiency, 300653 (3)

    Green PGK1 in Red cell disorders


    Level 2: Haematological disorders
    Version 1.24

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • London South GLH
    • NHS GMS
    Phenotypes
    • Phosphoglycerate kinase 1 deficiency MIM# 300653

    Green PGK1 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
    • Phosphoglycerate kinase 1 deficiency, 300653 (3)

    Green PGK1 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
    • Phosphoglycerate kinase 1 deficiency, 300653 (3)