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Severe Paediatric Disorders

Gene: TPM4

Amber List (moderate evidence)

TPM4 (tropomyosin 4)
EnsemblGeneIds (GRCh38): ENSG00000167460
EnsemblGeneIds (GRCh37): ENSG00000167460
OMIM: 600317, Gene2Phenotype
TPM4 is in 3 panels

1 review

Louise Daugherty (Genomics England Curator)

I don't know

Initial gene list (NGC_genelist-20190823_GREEN_dis_moi_forCuration_20200211.xlsx) collated by Dr Courtney French (University of Cambridge University Hospital NHS Foundation), Dr Karyn Megy (Clinical Feedback Lead, NIHR BioResource - Rare Diseases Study, University of Cambridge University Hospital NHS Foundation), Dr Alba Sanchis-Juan (NIHR BioResource - Rare Diseases Study, University of Cambridge University Hospital NHS Foundation) and Lucy Raymond (Professor of Medical Genetics and Neurodevelopment, University of Cambridge University Hospital NHS Foundation). Submitted to the PanelApp resource January 2020 on behalf of the Next Generation Children Project, Addenbrookes' Hospital, Cambridge. Gene Symbol submitted: TPM4; Recommended initial gene rating: I don't know; Phenotypes: ?Myasthenic syndrome, congenital, 18, 616330 (3); Mode of inheritance: Autosomal dominant
Created: 20 Feb 2020, 5:28 p.m. | Last Modified: 20 Feb 2020, 5:28 p.m.
Panel Version: 0.12

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Next Generation Children Project
  • Expert Review Amber
  • Expert list
Phenotypes
  • ?Myasthenic syndrome, congenital, 18, 616330
OMIM
600317
Clinvar variants
Variants in TPM4
Penetrance
None
Publications
Panels with this gene

History Filter Activity

20 Feb 2020, Gel status: 2

Set publications

Louise Daugherty (Genomics England Curator)

Publications for gene TPM4 were updated from to 30847515

20 Feb 2020, Gel status: 2

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Added phenotypes ?Myasthenic syndrome, congenital, 18, 616330 for gene: TPM4

20 Feb 2020, Gel status: 2

Set Phenotypes