PanelApp
  1. Genes and Genomic Entities
  2. RNF170

RNF170

ring finger protein 170
OMIM: 614649, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green RNF170 in Mendeliome


Version 1.3512

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Spastic paraplegia 85, autosomal recessive, MIM# 619686
  • Ataxia, sensory, 1, autosomal dominant, MIM# 608984

Green RNF170 in Ataxia - adult onset


Level 2: Neurology and neurodevelopmental disorders
Version 1.59

Component of the following Super Panels:

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

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Ataxia, sensory, 1, autosomal dominant, MIM# 608984

    Green RNF170 in Hereditary Spastic Paraplegia - paediatric


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.102

    Component of the following Super Panels:

  • Hereditary Spastic Paraplegia Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Spastic paraplegia 85, autosomal recessive, MIM# 619686