Genomics England
GMS Panels
Panels
Genes and Entities

GLI2

GLI family zinc finger 2
OMIM: 165230
PanelMode of inheritanceDetails
7 panels
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 7.8
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Culler-Jones syndrome, OMIM:615849, Holoprosencephaly 9, OMIM:610829
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 8.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
GLI2-RELATED HOLOPROSENCEPHALY 261768
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 8.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
GLI2-RELATED HOLOPROSENCEPHALY
Green
in Holoprosencephaly
Component of the following Super Panels:
  • - Cerebral malformation
  • - Paediatric disorders
R-numbers: R85
Signed-off version 6.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Holoprosencephaly-9, Holoprosencephaly, Holoprosencephaly 9, 610829
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
Holoprosencephaly-9, 610829, GLI2-RELATED HOLOPROSENCEPHALY
Green
in Limb disorders
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 9.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Holoprosencephaly 9 610829, Culler-Jones syndrome 615849, Polydactyly
Green
in Pituitary hormone deficiency
R-numbers: R159
Signed-off version 4.10
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Culler-Jones syndrome (615849), Holoprosencephaly 9 (610829)