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MET - MET proto-oncogene, receptor tyrosine kinase
- Synonym(s) : DFNB97, hepatocyte growth factor receptor, HGFR, RCCP2
- Previous symbols and names : met proto-oncogene
- Type : gene with protein product
- Chromosomal location : 7q31
- OMIM: 164860
- HGNC: 7029
- UniProtKB: P08581
- Genatlas: MET
- Ensembl: ENSG00000105976
- IUPHAR-DB: 1815
- Reactome: P08581
- LOVD: MET
Diseases list
- Disease-causing germline mutation(s) in Autosomal recessive non-syndromic sensorineural deafness type DFNB
ORPHA:90636 
- Disease-causing germline mutation(s) in Hereditary papillary renal cell carcinoma
ORPHA:47044 - Disease-causing germline mutation(s) (gain of function) in Osteofibrous dysplasia
ORPHA:488265 - Disease-causing somatic mutation(s) in Papillary renal cell carcinoma
ORPHA:319298 - Disease-causing somatic mutation(s) in Pediatric hepatocellular carcinoma
ORPHA:33402 - Major susceptibility factor in NON RARE IN EUROPE: Autism
ORPHA:106 - Candidate gene tested in Selection of therapeutic option in non-small cell lung carcinoma
ORPHA:357191
: AssessedGene included in a panel of genes performed as part of a diagnostic test
Additional information
Patient-centred resources for this gene
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