Description
This panel was developed by and is maintained by VCGS.

5 reviewers

  • Ivan Macciocca (Victorian Clinical Genetics Services)

  • Ain Roesley (Victorian Clinical Genetics Services)

  • Sangavi Sivagnanasundram (Melbourne Health)

  • Daniel Flanagan (Victorian Clinical Genetics Services)

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

8 Entities

8 reviewed, 6 green

List Entity Reviews Mode of inheritance Details
8 Entitiess
Green Green List (high evidence)
CALM1
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Long QT syndrome 14 616247
  • Ventricular tachycardia, catecholaminergic polymorphic, 4 614916
Tags
Green Green List (high evidence)
CALM2
1 review
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Long QT syndrome 15 616249
  • sudden unexplained death
  • idopathic VF
Tags
Green Green List (high evidence)
CASQ2
2 reviews
2 green
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ventricular tachycardia, catecholaminergic polymorphic, 2, MIM# 611938
Tags
  • treatable
Green Green List (high evidence)
RYR2
1 review
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Ventricular tachycardia, catecholaminergic polymorphic, 1 604772
Tags
Green Green List (high evidence)
TECRL
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Ventricular tachycardia, catecholaminergic polymorphic, 3, MIM# 614021
Tags
Green Green List (high evidence)
TRDN
2 reviews
2 green
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Triadin knockout syndrome
  • CPVT
  • atypical LQTS phenotype
Tags
Amber Amber List (moderate evidence)
CALM3
3 reviews
1 green 1 red
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Ventricular tachycardia, catecholaminergic polymorphic 6, MIM# 618782
Tags
Red Red List (low evidence)
KCNJ2
2 reviews
1 red
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • catecholaminergic polymorphic ventricular tachycardia MONDO:0017990
Tags

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