Genomics England
GMS Panels
Panels
Genes and Entities

FOXE3

forkhead box E3
OMIM: 601094
PanelMode of inheritanceDetails
4 panels
Green
in Bilateral congenital or childhood onset cataracts
R-numbers: R31
Signed-off version 5.4
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Cataract 34, multiple types, OMIM:612968, cataract 34 multiple types, MONDO:0013067, Peter's anomaly, microphthalmia.
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
CONGENITAL PRIMARY APHAKIA 610256, ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS 107250
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Anterior segment dysgenesis 2, multiple subtypes, OMIM:610256, Cataract 34, multiple types, OMIM:612968, {Aortic aneurysm, familial thoracic 11, susceptibility to}, OMIM:617349 CONGENITAL PRIMARY APHAKIA, ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS
Green
in Structural eye disease
R-numbers: R36
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Anterior segment mesenchymal dysgenesis, OMIM:107250, Anterior segment dysgenesis 2, multiple subtypes, OMIM:610256