PRX

periaxin
OMIM: 605725, ClinGen, DECIPHER

8 panels

Panel Reviews Mode of inheritance Details
8 panels

Green PRX in Cataract


Level 2: Ophthalmological disorders
Version 0.631

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Cataract, MONDO:0005129, PRX-related

Green PRX in Mendeliome


Version 1.4541

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Charcot-Marie-Tooth disease type 4 MONDO:0018995
  • Cataract, MONDO:0005129, PRX-related

Red PRX in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.699

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Charcot-Marie-Tooth disease, type 4F, MIM#614895

Green PRX in Hereditary Neuropathy


Level 2: Neurology and neurodevelopmental disorders
Version 1.186

Component of the following Super Panels:

  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Royal Melbourne Hospital
    • Expert Review Green
    • Expert Review Green
    Phenotypes
    • Charcot-Marie-Tooth disease type 4 MONDO:0018995

    Green PRX in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.111

    0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Dejerine-Sottas disease, 145900 (3)

    Green PRX in Additional findings_Paediatric


    Level 2: Screening
    Version 0.280

    0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Charcot-Marie-Tooth disease

    Green PRX in Prepair 1000+


    Level 2: Screening
    Version 2.15

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Charcot-Marie-Tooth disease, type 4F, MIM# 614895
    • Dejerine-Sottas disease, MIM# 145900

    Red PRX in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.147

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category A gene
    Phenotypes
    • Charcot-Marie-Tooth disease, type 4F, MIM# 614895
    • Dejerine-Sottas disease, MIM# 145900