Genomics England
GMS Panels
Panels
Genes and Entities

FOXC1

forkhead box C1
OMIM: 601090
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
IRIDOGONIODYSGENESIS ANOMALY 601631, AXENFELD-RIEGER SYNDROME TYPE 3 602482, PETERS ANOMALY 604229
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
IRIDOGONIODYSGENESIS ANOMALY, AXENFELD-RIEGER SYNDROME TYPE 3, PETERS ANOMALY
Green
in Sporadic aniridia
R-numbers: R38
Signed-off version 3.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Aniridia, MONDO:0019172
Green
in Structural eye disease
R-numbers: R36
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Axenfeld-Rieger syndrome, type 3 602482, Anterior segment dysgenesis 3, multiple subtypes 601631