UBR4

ubiquitin protein ligase E3 component n-recognin 4
OMIM: 609890, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Amber UBR4 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Episodic ataxia
  • progressive neurological deterioration

Red UBR4 in Regression


Level 2: Neurology and neurodevelopmental disorders
Version 0.556

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Episodic ataxia
  • progressive neurological deterioration

Red UBR4 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Episodic ataxia

Red UBR4 in Paroxysmal Dyskinesia


Level 2: Neurology and neurodevelopmental disorders
Version 0.131

Component of the following Super Panels:

  • Dystonia_Superpanel
  • Neuromuscular Superpanel
  • Tremors_Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • early onset episodic ataxia
    • nystagmus
    • myokymia
    • tremor

    Amber UBR4 in Ataxia - paediatric


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.26

    Component of the following Super Panels:

  • Ataxia_Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Royal Melbourne Hospital
    • Victorian Clinical Genetics Services
    Phenotypes
    • ?Episodic ataxia
    • Episodic ataxia type 8, 616055

    Amber UBR4 in Episodic Ataxia


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.1

    Component of the following Super Panels:

  • Ataxia_Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    • Victorian Clinical Genetics Services
    Phenotypes
    • Episodic ataxia type 8