TRPA1

transient receptor potential cation channel subfamily A member 1
OMIM: 604775, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green TRPA1 in Pain syndromes

Level 3: Channelopathies
Level 2: Neurology and neurodevelopmental disorders
Version 1.9

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Review
  • Literaure
Phenotypes
  • Episodic pain syndrome, familial, 615040
  • Familial episodic pain syndrome type I

Red TRPA1 in Paroxysmal central nervous system disorders


Version 1.10
Signed off v.1.2 on 27 Feb 2020

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • NHS GMS
  • London North GLH
  • Wessex and West Midlands GLH
Phenotypes
  • ?Episodic pain syndrome, familial, 1, 615040
  • Familial episodic pain syndrome type I

Green TRPA1 in Hereditary neuropathy

Level 3: Motor and Sensory Disorders of the PNS
Level 2: Neurology and neurodevelopmental disorders
Version 1.381

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • NHS GMS
  • London North GLH
Phenotypes
  • Episodic pain syndrome, familial, 1, 615040

Amber TRPA1 in Hereditary neuropathy NOT PMP22 copy number


Version 1.19
Signed off v.1.2 on 27 Feb 2020

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • London North GLH
  • NHS GMS
  • NHS GMS
  • London North GLH
Phenotypes
  • Episodic pain syndrome, familial, 1, 615040