Details for Gene MET

GENE NAME MET
CHROMOSOME 7
ENSEMBL ID ENSG00000105976
ENTREZ ID 4233
UNIPROT ACCESSION NUMBER P08581
GO MOLECULAR FUNCTION protein tyrosine kinase activity; protein binding
ESSENTIAL IN MOUSE Essential
PATHWAYS hsa05226; R-HSA-8851805; R-HSA-2219530; hsa05202; hsa01521; hsa05206; hsa05211; hsa05100; R-HSA-9006934; hsa04015; R-HSA-199418; R-HSA-5663202; hsa05200; hsa04010; hsa05223; R-HSA-5684996; R-HSA-8874081; R-HSA-8875555; R-HSA-162582; hsa04020; R-HSA-8865999; hsa04014; R-HSA-1266738; hsa05205; R-HSA-5663205; R-HSA-8876384; R-HSA-6807004; hsa05202; R-HSA-2219528; R-HSA-400685; R-HSA-8851907; hsa01521; hsa05206; hsa05230; hsa05211; hsa05225; hsa04151; hsa04360; hsa05226; hsa05120; hsa04510; R-HSA-73857; R-HSA-8986944; R-HSA-9022699; hsa04015; R-HSA-8875513; hsa04520; hsa05100; hsa05218; hsa04010; hsa05223; R-HSA-5673001; R-HSA-416550; hsa04020; R-HSA-8875878; R-HSA-6806942; hsa05144; R-HSA-8875656; R-HSA-9006925; hsa05200; R-HSA-1257604; R-HSA-8875360; hsa05205; R-HSA-8875791; R-HSA-212436; R-HSA-6811558; R-HSA-422475; hsa04014; R-HSA-5683057; R-HSA-9675108; hsa04151; hsa04360; R-HSA-1643685; hsa04510; hsa05120; hsa05230; hsa05225; hsa04520; hsa05218; R-HSA-6806834; R-HSA-373755; R-HSA-74160; hsa05144
3 combinations linked to MET OLI499; OLI906; OLI855
3 variants linked to MET MET:c.2975C>T, p.Thr992Ile; MET:c.1090G>A, p.Ala364Thr; MET:c.524G>C, p.Cys175Ser
4 diseases linked to MET Normosmic congenital hypogonadotropic hypogonadism; Congenital diaphragmatic hernia; Kallmann syndrome; Marfan syndrome
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