RAF1

Raf-1 proto-oncogene, serine/threonine kinase
OMIM: 164760, Gene2Phenotype

16 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 16 panels
Green RAF1 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.447	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green RAF1 in Hypertrophic cardiomyopathy_HCM Level 2: Cardiovascular disorders Version 1.3 Component of the following Super Panels: Adult Cardiac SuperPanel Cardiomyopathy_Adult_SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, dilated, 1NN MIM#615916 Noonan syndrome 5 MIM#611553
Green RAF1 in Hydrops fetalis Level 2: Dysmorphic and congenital abnormality syndromes Version 0.325	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Noonan syndrome 5, MIM# 611553
Green RAF1 in Macrocephaly_Megalencephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 0.150	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green RAF1 in Mendeliome Version 1.2656	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Noonan syndrome 5, MIM# 611553 Cardiomyopathy, dilated, 1NN, MIM# 615916
Green RAF1 in Cancer Predisposition_Paediatric Level 2: Cancer Version 0.131	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green RAF1 in Rasopathy Level 2: Dysmorphic and congenital abnormality syndromes Version 0.107	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Noonan syndrome 5, MIM# 611553
Green RAF1 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.545	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green RAF1 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.215	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Noonan Syndrome with Multiple Lentigines, OMIM # 611554
Green RAF1 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.174	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genetic Health Queensland Phenotypes Noonan syndrome 5, MIM# 611553
Green RAF1 in Lymphoedema_syndromic Level 3: Lymphatic Disorders Level 2: Cardiovascular disorders Version 0.12 Component of the following Super Panels: Vascular Malformations SuperPanel	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Expert Review Phenotypes Noonan syndrome 5 611553 LEOPARD syndrome 2 611554
Green RAF1 in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.197	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green South West GLH NHS GMS Expert List London South GLH Phenotypes Cardiomyopathy, dilated, 1NN, MIM# 615916 Noonan syndrome 5, MIM# 611553
Green RAF1 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Noonan syndrome
Green RAF1 in Growth failure Version 1.77	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Noonan syndrome 5, MIM# 611553
Green RAF1 in Fetal anomalies Version 1.370	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genomics England PanelApp Victorian Clinical Genetics Services Phenotypes Noonan syndrome 5, MIM# 611553
Red RAF1 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.121	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category A gene Phenotypes Noonan syndrome 5, MIM# 611553