Genomics England

GLI3

GLI family zinc finger 3

Panel	Mode of inheritance	Details
Filter panels12 panels
Green in Clefting Component of the following Super Panels: - Paediatric disorders Signed-off version 6.1	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Pallister-Hall syndrome, OMIM:146510
Green in DDG2P Component of the following Super Panels: - Paediatric disorders Signed-off version 4.15	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes PREAXIAL POLYDACTYLY TYPE IV 269157, GREIG CEPHALOPOLYSYNDACTYLY SYNDROME 175700, POSTAXIAL POLYDACTYLY TYPE A 174200, PALLISTER-HALL SYNDROME 146510
Green in Fetal anomalies R-numbers: R21, R412 Signed-off version 4.195	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Greig cephalopolysyndactyly syndrome, OMIM:175700, Pallister-Hall syndrome, OMIM:146510, Polydactyly, postaxial, types A1 and B, OMIM:174200, Polydactyly, preaxial, type IV, OMIM:174700
Green in Hydrocephalus R-numbers: R86 Signed-off version 5.0	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Greig cephalopolysyndactyly syndrome, OMIM:175700
Green in Limb disorders Component of the following Super Panels: - Paediatric disorders Signed-off version 6.2	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Greig cephalopolysyndactyly syndrome, OMIM:175700, Pallister-Hall syndrome, OMIM:146510, Polydactyly, postaxial, types A1 and B, OMIM:174200, Polydactyly, preaxial, type IV, OMIM:174700
Green in Neurological ciliopathies Component of the following Super Panels: - Hereditary ataxia and cerebellar anomalies - childhood onset - Paediatric disorders - Rare multisystem ciliopathy Super panel Signed-off version 4.10	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Greig cephalopolysyndactyly syndrome, OMIM:175700, Pallister-Hall syndrome, OMIM:146510
Green in Ophthalmological ciliopathies Component of the following Super Panels: - Paediatric disorders - Rare multisystem ciliopathy Super panel Signed-off version 4.5	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Greig cephalopolysyndactyly syndrome, OMIM:175700, Pallister-Hall syndrome, OMIM:146510
Green in Pituitary hormone deficiency R-numbers: R159 Signed-off version 3.0	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Greig cephalopolysyndactyly syndrome (175700), Pallister-Hall syndrome (146510)
Green in Rare syndromic craniosynostosis or isolated multisuture synostosis R-numbers: R100 Signed-off version 5.0	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Greig cephalopolysyndactyly syndrome, OMIM:175700
Green in Skeletal ciliopathies Component of the following Super Panels: - Paediatric disorders - Rare multisystem ciliopathy Super panel Signed-off version 5.1	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Greig cephalopolysyndactyly syndrome, OMIM:175700, Pallister-Hall syndrome, OMIM:146510
Green in Skeletal dysplasia Component of the following Super Panels: - Paediatric disorders R-numbers: R104 Signed-off version 6.16	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Greig cephalopolysyndactyly syndrome, OMIM:175700, Pallister-Hall syndrome, OMIM:146510, Polydactyly, postaxial, types A1 and B, OMIM:174200, Polydactyly, preaxial, type IV, OMIM:174700
Green in Unexplained young onset end-stage renal disease - additional genes Component of the following Super Panels: - Unexplained young onset end-stage renal disease Signed-off version 1.0	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Pallister-Hall syndrome, OMIM:146510