KEGG   VARIANT: 4233v5
Entry
4233v5                      Variant                                
Name
MET mutation
Type
Loss of function
Gene
MET  MET proto-oncogene, receptor tyrosine kinase [KO:K05099]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 164860
Network
nt06528  Calcium signaling
Disease
H00605  Deafness, autosomal recessive
Reference
PMID:25941349
  Authors
Mujtaba G, Schultz JM, Imtiaz A, Morell RJ, Friedman TB, Naz S
  Title
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss.
  Journal
J Med Genet 52:548-52 (2015)
DOI:10.1136/jmedgenet-2015-103023
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