PABPN1

poly(A) binding protein nuclear 1
OMIM: 602279, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green PABPN1 in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Oculopharyngeal muscular dystrophy - MIM#164300
Tags
  • STR

Green PABPN1 in Limb-Girdle Muscular Dystrophy and Distal Myopathy


Level 2: Neurology and neurodevelopmental disorders
Version 1.27

Component of the following Super Panels:

  • Myopathy Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Other
    Phenotypes
    • oculopharyngeal muscular dystrophy MONDO:0008116

    Red PABPN1 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Oculopharyngeal muscular dystrophy

    Red PABPN1 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Oculopharyngeal muscular dystrophy

    Green OPMD STR in Repeat Disorders


    Version 0.167

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Oculopharyngeal muscular dystrophy MIM#164300
    Tags
    • adult-onset