PHKA1

phosphorylase kinase regulatory subunit alpha 1
OMIM: 311870, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green PHKA1 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
    • Muscle glycogenosis, MIM# 300559

    Green PHKA1 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
    • Muscle glycogenosis, MIM# 300559

    Green PHKA1 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
    • Royal Melbourne Hospital
    • Victorian Clinical Genetics Services
    Phenotypes
    • Muscle glycogenosis, MIM# 300559

    Red PHKA1 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
    Phenotypes
    • Phosphorylase kinase deficiency

    Red PHKA1 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Phosphorylase kinase deficiency