MET

MET proto-oncogene, receptor tyrosine kinase
OMIM: 164860, Gene2Phenotype

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Amber MET in Arthrogryposis Level 2: Neurology and neurodevelopmental disorders Version 0.416	review	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 0.205	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Victorian Clinical Genetics Services Phenotypes ?Deafness, autosomal recessive 97, OMIM #616705 {Osteofibrous dysplasia, susceptibility to}, OMIM #607278
Green MET in Mendeliome Version 1.2302	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 1.210	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 1.63	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Phenotypes ?Deafness, autosomal recessive 97, OMIM #616705 {Osteofibrous dysplasia, susceptibility to}, OMIM #607278
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	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert list
Amber MET in Vascular Malformations_Somatic Level 2: Cardiovascular disorders Version 1.14 Component of the following Super Panels: Vascular Malformations SuperPanel	review	Other	Sources Expert Review Amber Literature Phenotypes lymphovenous malformation overgrowth
Green MET in Incidentalome_PREGEN_DRAFT Version 0.43	review	Unknown	Sources NSW Health Pathology Expert Review Green
Green MET in Kidney Cancer Level 2: Cancer Predisposition Version 1.1	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert list Phenotypes Renal carcinoma, MONDO:0005206 Papillary renal cell carcinoma, MONDO:0017884 Renal cell carcinoma, papillary, 1, familial, MIM#605074