| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 4296 |
Name | MAP3K11 |
Synonymous | mitogen-activated protein kinase kinase kinase 11;MAP3K11;mitogen-activated protein kinase kinase kinase 11 |
Definition | SH3 domain-containing proline-rich kinase|mixed lineage kinase 3|protein-tyrosine kinase PTK1|src-homology 3 domain-containing proline-rich kinase |
Position | 11q13.1-q13.3 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1269G>A; p.E423E; 11:65607490-65607490 |
breast | carcinoma | Substitution - coding silent |
c.2471_2472insG; p.Q826fs*>23; 11:65598363-65598364 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.2006G>A; p.R669H; 11:65599594-65599594 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2427A>C; p.S809S; 11:65598408-65598408 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2270G>A; p.R757H; 11:65598565-65598565 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.445G>A; p.D149N; 11:65613312-65613312 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2270G>A; p.R757H; 11:65598565-65598565 |
ovary | other; neoplasm | Substitution - Missense |
c.2046G>A; p.T682T; 11:65599554-65599554 |
lung | carcinoma; small_cell_carcinoma | Substitution - coding silent |
c.965A>G; p.Y322C; 11:65608026-65608026 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2063C>T; p.T688I; 11:65599537-65599537 |
skin | malignant_melanoma | Substitution - Missense |
c.308delG; p.G103fs*20; 11:65613449-65613449 |
lung | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.451G>A; p.D151N; 11:65613306-65613306 |
breast | carcinoma | Substitution - Missense |
c.2106G>A; p.T702T; 11:65599494-65599494 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2117C>T; p.P706L; 11:65599483-65599483 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.608G>A; p.R203Q; 11:65613149-65613149 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1648delC; p.R550fs*51; 11:65606037-65606037 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.968G>A; p.R323H; 11:65608023-65608023 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.968G>A; p.R323H; 11:65608023-65608023 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.364G>A; p.V122M; 11:65613393-65613393 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.1831G>T; p.G611C; 11:65605761-65605761 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.440G>A; p.R147H; 11:65613317-65613317 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2060C>T; p.P687L; 11:65599540-65599540 |
skin | malignant_melanoma | Substitution - Missense |
c.2060C>T; p.P687L; 11:65599540-65599540 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2189G>A; p.R730H; 11:65599411-65599411 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.915C>T; p.V305V; 11:65608273-65608273 |
skin | malignant_melanoma | Substitution - coding silent |
c.2037C>T; p.P679P; 11:65599563-65599563 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.312C>T; p.G104G; 11:65613445-65613445 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.312C>T; p.G104G; 11:65613445-65613445 |
thyroid | other; neoplasm | Substitution - coding silent |
c.2047C>T; p.P683S; 11:65599553-65599553 |
skin; upper_leg | malignant_melanoma | Substitution - Missense |
c.2135T>A; p.L712Q; 11:65599465-65599465 |
liver | carcinoma | Substitution - Missense |
c.2135T>A; p.L712Q; 11:65599465-65599465 |
liver | carcinoma | Substitution - Missense |
c.291C>T; p.S97S; 11:65613466-65613466 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1729C>T; p.Q577*; 11:65605956-65605956 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1729C>T; p.Q577*; 11:65605956-65605956 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1771T>C; p.Y591H; 11:65605821-65605821 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.789G>A; p.L263L; 11:65608399-65608399 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.789G>A; p.L263L; 11:65608399-65608399 |
breast | carcinoma; HER-positive_carcinoma | Substitution - coding silent |
c.12G>A; p.L4L; 11:65613745-65613745 |
breast | carcinoma; HER-positive_carcinoma | Substitution - coding silent |
c.1263G>A; p.E421E; 11:65607496-65607496 |
skin | malignant_melanoma | Substitution - coding silent |
c.668C>T; p.A223V; 11:65613089-65613089 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.740-1G>T; p.?; 11:65608449-65608449 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Unknown |
c.530T>C; p.I177T; 11:65613227-65613227 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.377G>A; p.G126E; 11:65613380-65613380 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.128A>G; p.N43S; 11:65613629-65613629 |
pancreas | carcinoma | Substitution - Missense |
c.360G>A; p.E120E; 11:65613397-65613397 |
skin | malignant_melanoma | Substitution - coding silent |
c.512T>G; p.L171R; 11:65613245-65613245 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.512T>G; p.L171R; 11:65613245-65613245 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1364G>A; p.R455H; 11:65607395-65607395 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1993_1994GG>AA; p.G665K; 11:65599606-65599607 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2405C>T; p.P802L; 11:65598430-65598430 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1204G>C; p.E402Q; 11:65607682-65607682 |
skin | malignant_melanoma | Substitution - Missense |
c.623G>A; p.R208Q; 11:65613134-65613134 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.930G>A; p.V310V; 11:65608061-65608061 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2329G>T; p.D777Y; 11:65598506-65598506 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1003G>A; p.A335T; 11:65607988-65607988 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.885G>A; p.K295K; 11:65608303-65608303 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1341G>A; p.Q447Q; 11:65607418-65607418 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1102G>C; p.D368H; 11:65607784-65607784 |
parathyroid | carcinoma | Substitution - Missense |
c.1123C>G; p.Q375E; 11:65607763-65607763 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1393G>A; p.D465N; 11:65607366-65607366 |
liver | carcinoma | Substitution - Missense |
c.845C>T; p.A282V; 11:65608343-65608343 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2476delC; p.Q826fs*>22; 11:65598359-65598359 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1393G>A; p.D465N; 11:65607366-65607366 |
liver | carcinoma | Substitution - Missense |
c.1200G>A; p.K400K; 11:65607686-65607686 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.2513A>G; p.Q838R; 11:65598322-65598322 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1092C>T; p.H364H; 11:65607794-65607794 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.496C>G; p.R166G; 11:65613261-65613261 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1807C>T; p.P603S; 11:65605785-65605785 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.484C>T; p.R162C; 11:65613273-65613273 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.694G>T; p.E232*; 11:65613063-65613063 |
liver | carcinoma | Substitution - Nonsense |
c.526A>G; p.I176V; 11:65613231-65613231 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.526A>G; p.I176V; 11:65613231-65613231 |
lung | carcinoma; bronchioloalveolar_adenocarcinoma | Substitution - Missense |
c.2024C>T; p.P675L; 11:65599576-65599576 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.997G>A; p.G333S; 11:65607994-65607994 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2050G>A; p.A684T; 11:65599550-65599550 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2036C>T; p.P679L; 11:65599564-65599564 |
skin | malignant_melanoma | Substitution - Missense |
c.2036C>T; p.P679L; 11:65599564-65599564 |
skin | malignant_melanoma | Substitution - Missense |
c.56G>A; p.S19N; 11:65613701-65613701 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.858C>T; p.Y286Y; 11:65608330-65608330 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.910G>A; p.D304N; 11:65608278-65608278 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.735C>T; p.N245N; 11:65613022-65613022 |
liver | carcinoma | Substitution - coding silent |
c.1221C>T; p.F407F; 11:65607665-65607665 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1221C>T; p.F407F; 11:65607665-65607665 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.735C>T; p.N245N; 11:65613022-65613022 |
liver | carcinoma | Substitution - coding silent |
c.1054G>T; p.A352S; 11:65607937-65607937 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.656C>T; p.A219V; 11:65613101-65613101 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1585C>T; p.R529W; 11:65606709-65606709 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1988C>T; p.P663L; 11:65599612-65599612 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1184T>A; p.M395K; 11:65607702-65607702 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - Missense |
c.2049C>T; p.P683P; 11:65599551-65599551 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.674G>A; p.G225E; 11:65613083-65613083 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.628G>A; p.V210M; 11:65613129-65613129 |
breast | carcinoma; HER-positive_carcinoma | Substitution - Missense |
c.1163C>T; p.P388L; 11:65607723-65607723 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.847G>A; p.A283T; 11:65608341-65608341 |
skin | malignant_melanoma | Substitution - Missense |
c.2421G>A; p.P807P; 11:65598414-65598414 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2156C>G; p.P719R; 11:65599444-65599444 |
liver | carcinoma | Substitution - Missense |
c.1558G>A; p.G520R; 11:65606736-65606736 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2534C>T; p.A845V; 11:65598301-65598301 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2351C>T; p.A784V; 11:65598484-65598484 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2205C>T; p.R735R; 11:65599395-65599395 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1150C>T; p.L384L; 11:65607736-65607736 |
skin | malignant_melanoma | Substitution - coding silent |
c.1225G>A; p.E409K; 11:65607661-65607661 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.2037delC; p.T680fs*>168; 11:65599563-65599563 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1742G>A; p.R581K; 11:65605850-65605850 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.2070G>T; p.P690P; 11:65599530-65599530 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.2039C>T; p.T680M; 11:65599561-65599561 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1080G>A; p.A360A; 11:65607806-65607806 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2048C>T; p.P683L; 11:65599552-65599552 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1133C>T; p.A378V; 11:65607753-65607753 |
ovary | other; neoplasm | Substitution - Missense |
c.1133C>T; p.A378V; 11:65607753-65607753 |
ovary | other; neoplasm | Substitution - Missense |
c.907A>G; p.S303G; 11:65608281-65608281 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.69T>G; p.G23G; 11:65613688-65613688 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.511C>T; p.L171L; 11:65613246-65613246 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.2079C>T; p.S693S; 11:65599521-65599521 |
skin | malignant_melanoma | Substitution - coding silent |
c.2118G>A; p.P706P; 11:65599482-65599482 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.358G>T; p.E120*; 11:65613399-65613399 |
breast | carcinoma | Substitution - Nonsense |
c.2543G>C; p.*848S; 11:65598292-65598292 |
breast | carcinoma | Nonstop extension |
c.1948G>A; p.A650T; 11:65599652-65599652 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2228C>T; p.P743L; 11:65598607-65598607 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1841delC; p.P614fs*27; 11:65599759-65599759 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1841delC; p.P614fs*27; 11:65599759-65599759 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.2301T>A; p.P767P; 11:65598534-65598534 |
skin | malignant_melanoma | Substitution - coding silent |
c.960G>A; p.V320V; 11:65608031-65608031 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2073C>T; p.P691P; 11:65599527-65599527 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1750C>T; p.R584C; 11:65605842-65605842 |
central_nervous_system; medulla | glioma; oligodendroglioma_Grade_III | Substitution - Missense |
c.439C>T; p.R147C; 11:65613318-65613318 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.439C>T; p.R147C; 11:65613318-65613318 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1709C>T; p.S570F; 11:65605976-65605976 |
skin | malignant_melanoma | Substitution - Missense |
c.1044C>T; p.P348P; 11:65607947-65607947 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1709C>T; p.S570F; 11:65605976-65605976 |
skin | malignant_melanoma | Substitution - Missense |
c.1961C>T; p.S654L; 11:65599639-65599639 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1710C>T; p.S570S; 11:65605975-65605975 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.324C>G; p.P108P; 11:65613433-65613433 |
ovary | other; neoplasm | Substitution - coding silent |
c.1931C>T; p.A644V; 11:65599669-65599669 |
ovary | other; neoplasm | Substitution - Missense |
c.324C>G; p.P108P; 11:65613433-65613433 |
ovary | other; neoplasm | Substitution - coding silent |
c.324C>G; p.P108P; 11:65613433-65613433 |
ovary | other; neoplasm | Substitution - coding silent |
c.324C>G; p.P108P; 11:65613433-65613433 |
ovary | other; neoplasm | Substitution - coding silent |
c.251G>T; p.W84L; 11:65613506-65613506 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1239G>C; p.K413N; 11:65607647-65607647 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1115T>C; p.I372T; 11:65607771-65607771 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.957G>A; p.E319E; 11:65608034-65608034 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.688C>T; p.H230Y; 11:65613069-65613069 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1731G>C; p.Q577H; 11:65605954-65605954 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.688C>T; p.H230Y; 11:65613069-65613069 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1976G>A; p.R659H; 11:65599624-65599624 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.2240G>A; p.R747H; 11:65598595-65598595 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.543T>G; p.A181A; 11:65613214-65613214 |
liver | carcinoma | Substitution - coding silent |
c.543T>G; p.A181A; 11:65613214-65613214 |
liver | carcinoma | Substitution - coding silent |
c.1647C>T; p.P549P; 11:65606038-65606038 |
skin | malignant_melanoma | Substitution - coding silent |