Genomics England
GMS Panels
Panels
Genes and Entities

BCL11A

B-cell CLL/lymphoma 11A
OMIM: 606557
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 8.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
BCL11A-related intellectual disability, Dias-Logan syndrome, OMIM:617101
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 8.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Dias-Logan syndrome, OMIM:617101, Dias-Logan syndrome, MONDO:0014914, BCL11A-related intellectual developmental disorder with persistence of fetal hemoglobin
Green
in Intellectual disability
Component of the following Super Panels:
  • - Hypotonic infant
  • - Leukodystrophy, childhood onset
  • - Paediatric disorders
Signed-off version 11.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Dias-Logan syndrome, OMIM:617101, Dias-Logan syndrome, MONDO:0014914, BCL11A-related intellectual developmental disorder with persistence of fetal hemoglobin