PanelApp (stage)
  1. Genes and Genomic Entities
  2. SNCA

SNCA

synuclein alpha
OMIM: 163890, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green SNCA in Early-onset Dementia


Level 2: Neurology and neurodevelopmental disorders
Version 1.24

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Complex Neurology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Dementia, Lewy body (MIM#127750)
    • Parkinson disease 1 (MIM#168601)
    • Parkinson disease 4 (MIM#605543)

    Green SNCA 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 MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Complex Neurology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Dementia, Lewy body (MIM#127750)
    • Parkinson disease 1 (MIM#168601)
    • Parkinson disease 4 (MIM#605543)
    Tags
    • SV/CNV

    Green SNCA in Incidentalome


    Version 0.301

    		review MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Dementia, Lewy body (MIM#127750)
    • Parkinson disease 1 (MIM#168601)
    • Parkinson disease 4 (MIM#605543)
    Tags
    • SV/CNV

    Green SNCA in Incidentalome_PREGEN_DRAFT


    Version 0.43

    		review Unknown
    Sources
    • NSW Health Pathology
    • Expert Review Green