PanelApp
  1. Genes and Genomic Entities
  2. PDYN

PDYN

prodynorphin
OMIM: 131340, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green PDYN in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Spinocerebellar ataxia 23 - MIM#610245

Green PDYN in Callosome


Level 2: Neurology and neurodevelopmental disorders
Version 0.540

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green PDYN in Regression


Level 2: Neurology and neurodevelopmental disorders
Version 0.573

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green PDYN in Ataxia - adult onset


Level 2: Neurology and neurodevelopmental disorders
Version 1.20

Component of the following Super Panels:

  • Ataxia_Superpanel
  • Neurodegenerative disease - adult onset
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Spinocerebellar ataxia 23
    • Spinocerebellar ataxia 23, 610245

    Green PDYN in Hereditary Neuropathy - complex


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.19

    Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Spinocerebellar ataxia 23 (MIM#610245)
    • Cerebellar ataxia, sensory-motor axonal neuropathy
    • Spinocerebellar ataxia 23