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  2. Episodic Ataxia

Episodic Ataxia (Version 1.1)

Level 2: Neurology and neurodevelopmental disorders

Relevant disorders: Ataxia, HP:0001251
Panel types: Victorian Clinical Genetics Services, Royal Melbourne Hospital, Rare Disease
Description
This panel contains genes that cause episodic ataxia. It was created and is maintained by RMH and is a consensus panel used by VCGS.
Panel Activity

4 reviewers

  • Eunice Chan (Royal Children's Hospital)

  • Michelle Torres (Victorian Clinical Genetics Services)

  • Bryony Thompson (Royal Melbourne Hospital)

  • Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

7 Entities

7 reviewed, 5 green

List Entity Reviews Mode of inheritance Details
7 Entitiess
Green List (high evidence)
BCKDHB
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Episodic ataxia during metabolic crises
  • paroxysmal nonkinesigenic dyskinesia
Tags
  • treatable
Green List (high evidence)
CACNA1A
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Episodic ataxia, type 2 MIM#108500
Tags
  • STR
Green List (high evidence)
FGF14
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Episodic Ataxia type 9
Tags
Green List (high evidence)
KCNA1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Episodic ataxia/myokymia syndrome MIM#160120
  • EA1
Tags
Green List (high evidence)
SLC1A3
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Episodic ataxia, type 6 MIM#612656
Tags
Amber List (moderate evidence)
UBR4
1 review
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
  • Victorian Clinical Genetics Services
Phenotypes
  • Episodic ataxia type 8
Tags
Red List (low evidence)
CACNB4
1 review
1 red
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Red
Phenotypes
  • Episodic ataxia, type 5 MIM#613855
Tags

Major version comments

  • 2022-11-23 04:39 Bryony Thompson (Royal Melbourne Hospital) promoted panel to 1.0
    All genes have been reviewed

Downloads

Download lists

  • Whole panel
  • Green list (high evidence)
  • Green and Amber Genes
  • Amber Genes
  • Red list (low evidence)

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