MET:Ensemblv90

MET proto-oncogene, receptor tyrosine kinase
OMIM: 164860, ClinGen, DECIPHER

14 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 14 panels
Amber MET in Arthrogryposis Level 2: Neurology and neurodevelopmental disorders Version 1.1 Component of the following Super Panels: Neuromuscular Superpanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Amber Literature Phenotypes ?Arthrogryposis, distal, type 11 (MIM#620019), AD
Red MET in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.233	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Victorian Clinical Genetics Services Phenotypes complex neurodevelopmental disorder, MONDO:0100038 Tags disputed
Green MET in Mendeliome Version 1.3802	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Arthrogryposis, distal, type 11 (MIM#620019), AD Renal cell carcinoma, papillary, 1, familial and somatic, MIM# 605074 Papillary renal cell carcinoma MONDO:0017884
Red MET in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.304	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Phenotypes Deafness, autosomal recessive 97, MIM# 616705
Red MET in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.508	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert list Phenotypes complex neurodevelopmental disorder, MONDO:0100038 Tags disputed
Red MET in NCGC Version 0.3	0 reviews	Other	Sources NCGC Phenotypes Renal cell carcinoma, papillary, 1
Red MET in TCGA_PANCAN_2018 Version 0.3	0 reviews	Other	Sources TCGA_PANCAN_2018 Phenotypes Renal cell carcinoma, papillary, 1
Red MET in Lymphoedema_syndromic Level 3: Lymphatic Disorders Level 2: Cardiovascular disorders Version 0.12 Component of the following Super Panels: Vascular Malformations SuperPanel	0 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert list
Amber MET in Vascular Malformations_Somatic Level 2: Cardiovascular disorders Version 1.16 Component of the following Super Panels: Vascular Malformations SuperPanel	1 review	Other	Sources Expert Review Amber Literature Phenotypes lymphovenous malformation overgrowth
Green MET in Renal cancer Level 2: Cancer susceptibility Version 0.5	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green SA Pathology Phenotypes Hereditary papillary renal carcinoma with type 1 papillary tumors
Green MET in Incidentalome_PREGEN_DRAFT Version 0.43	0 reviews	Unknown	Sources NSW Health Pathology Expert Review Green
Red MET in Autism Level 2: Neurology and neurodevelopmental disorders Version 1.0	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Expert list Expert Review Red Phenotypes complex neurodevelopmental disorder, MONDO:0100038 Tags disputed
Red MET in Lymphoedema_syndromic Level 3: Lymphatic Disorders Level 2: Cardiovascular disorders Version 1.0	0 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert list
Green MET in Renal cancer Level 2: Cancer susceptibility Version 1.0	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources SA Pathology Expert Review Green Phenotypes Hereditary papillary renal carcinoma with type 1 papillary tumors