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Severe Paediatric Disorders

Gene: BCL10

Amber List (moderate evidence)

BCL10 (B-cell CLL/lymphoma 10)
EnsemblGeneIds (GRCh38): ENSG00000142867
EnsemblGeneIds (GRCh37): ENSG00000142867
OMIM: 603517, Gene2Phenotype
BCL10 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: BCL10; Recommended initial gene rating: I don't know; Phenotypes: ?Immunodeficiency 37, 616098 (3); Mode of inheritance: Autosomal recessive
Created: 20 Feb 2020, 5:27 p.m. | Last Modified: 20 Feb 2020, 5:27 p.m.
Panel Version: 0.12

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Next Generation Children Project
  • Expert Review Amber
  • Expert list
Phenotypes
  • ?Immunodeficiency 37, 616098
OMIM
603517
Clinvar variants
Variants in BCL10
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 BCL10 were updated from to 30847515

20 Feb 2020, Gel status: 2

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Added phenotypes ?Immunodeficiency 37, 616098 for gene: BCL10

20 Feb 2020, Gel status: 2

Set Phenotypes

Louise Daugherty (Genomics Engl