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  3. BCL11A
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Autism

Gene: BCL11A

Amber List (moderate evidence)
BCL11A (B-cell CLL/lymphoma 11A)
EnsemblGeneIds (GRCh38): ENSG00000119866
EnsemblGeneIds (GRCh37): ENSG00000119866
OMIM: 606557, Gene2Phenotype
BCL11A is in 4 panels

1 review

Louise Daugherty (Genomics England Curator)

I don't know

Each gene in the SFARI Human Gene module has a dedicated entry summary page, see here for more info on this gene: https://gene.sfari.org/database/human-gene/BCL11A Gene indicated by SFARI as predisposition to autism in the context of a syndromic disorder.
Created: 1 Apr 2019, 11:26 a.m.
Created: 1 Apr 2019, 11:26 a.m.

Panel version: 0.11

Details

Sources
  • Expert Review Amber
  • SFARI
OMIM
606557
Clinvar variants
Variants in BCL11A
Penetrance
None
Publications
Panels with this gene

History Filter Activity

1 Apr 2019, Gel status: 2

Set publications

Louise Daugherty (Genomics England Curator)

Publications for gene BCL11A were changed from to 20212079; 26185613; 23042784; 24267887; 26166478; 25989142; 24090431; 24581740; 26167905; 23999528; 25294932

29 Mar 2019, Gel status: 2

Added New Source, Status Update

Louise Daugherty (Genomics England Curator)

Source Expert Review Amber was added to BCL11A. Rating Changed from Red List (low evidence) to Amber List (moderate evidence)

29 Mar 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance

Louise Daugherty (Genomics England Curator)

gene: BCL11A was added gene: BCL11A was added to Autism. Sources: SFARI Mode of inheritance for gene: BCL11A was set to