LZTR1

leucine zipper like transcription regulator 1
OMIM: 600574, Gene2Phenotype

16 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 16 panels
Red LZTR1 in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.356	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Noonan syndrome 2, MIM#605275
Green LZTR1 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.418	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Cardiac defects hypertrophic cardiomyopathy atrial septal defect pulmonary stenosis short stature intellectual disabilities
Green LZTR1 in Hydrops fetalis Level 2: Dysmorphic and congenital abnormality syndromes Version 0.313	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Noonan syndrome 10 Noonan syndrome 2 {Schwannomatosis-2, susceptibility to}
Green LZTR1 in Incidentalome Version 0.301	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green LZTR1 in Macrocephaly_Megalencephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 0.140	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green LZTR1 in Rasopathy Level 2: Dysmorphic and congenital abnormality syndromes Version 0.105	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Noonan syndrome 10 Noonan syndrome 2
Green LZTR1 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.522	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green LZTR1 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 0.6063	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Noonan syndrome 10, MIM#616564 Noonan syndrome 2, MIM#605275
Red LZTR1 in CGC_86 Version 0.2	review	Other	Sources CGC_86 Phenotypes NA
Red LZTR1 in NCGC Version 0.2	review	Other	Sources NCGC Phenotypes NA
Green LZTR1 in Lymphoedema_syndromic Level 3: Lymphatic Disorders Level 2: Cardiovascular disorders Version 0.12 Component of the following Super Panels: Vascular Malformations SuperPanel	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Phenotypes Schwannomatosis-2, susceptibility to 615670 Noonan syndrome 10 616564
Green LZTR1 in Schwannomatosis Level 2: Neurology and neurodevelopmental disorders Version 0.16	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes {Schwannomatosis-2, susceptibility to} MIM#615670
Green LZTR1 in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.192	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert List NHS GMS Phenotypes Schwannomatosis-2, susceptibility to 615670 Noonan syndrome 10 616564
Green LZTR1 in Incidentalome_PREGEN_DRAFT Version 0.43	review	Unknown	Sources NSW Health Pathology Expert Review Green
Green LZTR1 in Growth failure Version 1.76	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Noonan syndrome 10 Noonan syndrome 2
Green LZTR1 in Fetal anomalies Version 1.255	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Expert list Phenotypes Noonan syndrome 10, MIM#616564 Noonan syndrome 2, MIM#605275 Fetal hydrops