| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 5609 |
Name | MAP2K7 |
Synonymous | mitogen-activated protein kinase kinase 7;MAP2K7;mitogen-activated protein kinase kinase 7 |
Definition | JNK-activating kinase 2|MAP kinase kinase 7|MAPK/ERK kinase 7|SAPK kinase 4|c-Jun N-terminal kinase kinase 2|dual specificity mitogen-activated protein kinase kinase 7|stress-activated protein kinase kinase 4 |
Position | 19p13.3-p13.2 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1133G>T; p.S378I; 19:7912304-7912304 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.748C>G; p.L250V; 19:7911052-7911052 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.484C>T; p.R162C; 19:7910489-7910489 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.484C>T; p.R162C; 19:7910489-7910489 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.484C>T; p.R162C; 19:7910489-7910489 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.484C>T; p.R162C; 19:7910489-7910489 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.922C>A; p.L308M; 19:7911316-7911316 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.824C>T; p.T275M; 19:7911128-7911128 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.265A>T; p.S89C; 19:7909895-7909895 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.824C>T; p.T275M; 19:7911128-7911128 |
ovary | other; neoplasm | Substitution - Missense |
c.824C>T; p.T275M; 19:7911128-7911128 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.824C>T; p.T275M; 19:7911128-7911128 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.573C>T; p.D191D; 19:7910701-7910701 |
breast | carcinoma | Substitution - coding silent |
c.646G>A; p.E216K; 19:7910774-7910774 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.458G>T; p.R153L; 19:7910463-7910463 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.573C>T; p.D191D; 19:7910701-7910701 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.458G>T; p.R153L; 19:7910463-7910463 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.516G>A; p.K172K; 19:7910521-7910521 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.22C>T; p.Q8*; 19:7903966-7903966 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.417C>T; p.F139F; 19:7910343-7910343 |
skin | malignant_melanoma | Substitution - coding silent |
c.333+2T>C; p.?; 19:7910131-7910131 |
endometrium | carcinoma; endometrioid_carcinoma | Unknown |
c.757G>A; p.E253K; 19:7911061-7911061 |
skin | malignant_melanoma | Substitution - Missense |
c.1080-1G>A; p.?; 19:7912148-7912148 |
skin | malignant_melanoma | Unknown |
c.1099A>T; p.K367*; 19:7912168-7912168 |
stomach | carcinoma; mixed_intestinal_and_diffuse_adenocarcinoma-unclassifiable | Substitution - Nonsense |
c.980C>T; p.T327M; 19:7911479-7911479 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.980C>T; p.T327M; 19:7911479-7911479 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.952G>T; p.G318*; 19:7911451-7911451 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.952G>T; p.G318*; 19:7911451-7911451 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.952G>T; p.G318*; 19:7911451-7911451 |
large_intestine; colon | carcinoma | Substitution - Nonsense |
c.952G>T; p.G318*; 19:7911451-7911451 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.329_330insG; p.Q111fs*39; 19:7910125-7910126 |
large_intestine; rectum | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.485G>A; p.R162H; 19:7910490-7910490 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.485G>A; p.R162H; 19:7910490-7910490 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.712G>T; p.G238C; 19:7911016-7911016 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.937-2A>C; p.?; 19:7911434-7911434 |
stomach | carcinoma; intestinal_adenocarcinoma | Unknown |
c.1049C>T; p.S350L; 19:7911548-7911548 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.40G>T; p.E14*; 19:7903984-7903984 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.870C>T; p.D290D; 19:7911264-7911264 |
ovary | other; neoplasm | Substitution - coding silent |
c.33C>T; p.S11S; 19:7903977-7903977 |
skin | malignant_melanoma | Substitution - coding silent |
c.1023G>A; p.P341P; 19:7911522-7911522 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1240C>T; p.H414Y; 19:7912411-7912411 |
skin | malignant_melanoma | Substitution - Missense |
c.534C>T; p.Y178Y; 19:7910539-7910539 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1172C>T; p.A391V; 19:7912343-7912343 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1225G>A; p.V409I; 19:7912396-7912396 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.896A>G; p.Y299C; 19:7911290-7911290 |
stomach | adenocarcinoma | Substitution - Missense |
c.381C>G; p.G127G; 19:7910307-7910307 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.743A>G; p.N248S; 19:7911047-7911047 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1059C>T; p.F353F; 19:7911558-7911558 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.937-9_937-8CC>TT; p.?; 19:7911427-7911428 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Unknown |
c.458G>A; p.R153H; 19:7910463-7910463 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.458G>A; p.R153H; 19:7910463-7910463 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.458G>A; p.R153H; 19:7910463-7910463 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.458G>A; p.R153H; 19:7910463-7910463 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.458G>A; p.R153H; 19:7910463-7910463 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.458G>A; p.R153H; 19:7910463-7910463 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.405G>A; p.W135*; 19:7910331-7910331 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.325delG; p.G110fs*62; 19:7910121-7910121 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.67G>A; p.E23K; 19:7904011-7904011 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.674C>T; p.A225V; 19:7910802-7910802 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.798C>T; p.G266G; 19:7911102-7911102 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.771C>T; p.I257I; 19:7911075-7911075 |
skin | malignant_melanoma | Substitution - coding silent |
c.463G>A; p.G155R; 19:7910468-7910468 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.457C>T; p.R153C; 19:7910462-7910462 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.457C>T; p.R153C; 19:7910462-7910462 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.937-1G>A; p.?; 19:7911435-7911435 |
large_intestine | carcinoma; adenocarcinoma | Unknown |
c.937-1G>A; p.?; 19:7911435-7911435 |
large_intestine | carcinoma; adenocarcinoma | Unknown |
c.1081C>T; p.L361F; 19:7912150-7912150 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.727G>A; p.D243N; 19:7911031-7911031 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.727G>A; p.D243N; 19:7911031-7911031 |
large_intestine; colon | adenoma | Substitution - Missense |
c.727G>A; p.D243N; 19:7911031-7911031 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.727G>A; p.D243N; 19:7911031-7911031 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.727G>A; p.D243N; 19:7911031-7911031 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.727G>A; p.D243N; 19:7911031-7911031 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.394G>C; p.G132R; 19:7910320-7910320 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.582C>T; p.I194I; 19:7910710-7910710 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.932C>T; p.S311L; 19:7911326-7911326 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.904C>T; p.R302W; 19:7911298-7911298 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.686C>T; p.A229V; 19:7910990-7910990 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.905G>T; p.R302L; 19:7911299-7911299 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.686C>T; p.A229V; 19:7910990-7910990 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.795C>A; p.S265R; 19:7911099-7911099 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1101G>A; p.K367K; 19:7912170-7912170 |
breast | carcinoma; HER-positive_carcinoma | Substitution - coding silent |
c.1125+1G>A; p.?; 19:7912195-7912195 |
large_intestine | carcinoma; adenocarcinoma | Unknown |
c.1125+1G>A; p.?; 19:7912195-7912195 |
large_intestine | carcinoma; adenocarcinoma | Unknown |
c.308C>T; p.T103M; 19:7910104-7910104 |
pancreas | carcinoma | Substitution - Missense |
c.308C>T; p.T103M; 19:7910104-7910104 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.14C>T; p.S5F; 19:7903958-7903958 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.725G>A; p.R242H; 19:7911029-7911029 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.5C>T; p.A2V; 19:7903949-7903949 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.454C>T; p.R152W; 19:7910459-7910459 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.725G>A; p.R242H; 19:7911029-7911029 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.844G>A; p.A282T; 19:7911148-7911148 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.355G>T; p.D119Y; 19:7910281-7910281 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.961C>T; p.P321S; 19:7911460-7911460 |
skin | malignant_melanoma | Substitution - Missense |
c.859G>A; p.E287K; 19:7911253-7911253 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.859G>A; p.E287K; 19:7911253-7911253 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.274_275insTT; p.D93fs*9; 19:7910070-7910071 |
breast | carcinoma | Insertion - Frameshift |
c.811T>A; p.S271T; 19:7911115-7911115 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.440C>T; p.A147V; 19:7910366-7910366 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.420G>A; p.R140R; 19:7910346-7910346 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.853G>A; p.A285T; 19:7911157-7911157 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.872_873CC>TT; p.P291L; 19:7911266-7911267 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.947C>A; p.A316E; 19:7911446-7911446 |
pancreas | carcinoma | Substitution - Missense |
c.781G>A; p.D261N; 19:7911085-7911085 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.826C>A; p.R276R; 19:7911130-7911130 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.781G>A; p.D261N; 19:7911085-7911085 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1033G>A; p.G345R; 19:7911532-7911532 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.781G>A; p.D261N; 19:7911085-7911085 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.385G>A; p.G129S; 19:7910311-7910311 |
pancreas | carcinoma | Substitution - Missense |
c.394G>A; p.G132S; 19:7910320-7910320 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.385G>A; p.G129S; 19:7910311-7910311 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.385G>A; p.G129S; 19:7910311-7910311 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1009C>T; p.Q337*; 19:7911508-7911508 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.913G>A; p.V305I; 19:7911307-7911307 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.354C>T; p.N118N; 19:7910280-7910280 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.856-8C>G; p.?; 19:7911242-7911242 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Unknown |
c.905G>A; p.R302Q; 19:7911299-7911299 |
oesophagus | carcinoma | Substitution - Missense |
c.538G>A; p.V180M; 19:7910543-7910543 |
pancreas | carcinoma | Substitution - Missense |
c.538G>A; p.V180M; 19:7910543-7910543 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.954A>G; p.G318G; 19:7911453-7911453 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.626G>A; p.R209Q; 19:7910754-7910754 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.461C>A; p.S154Y; 19:7910466-7910466 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Missense |
c.1156C>T; p.L386L; 19:7912327-7912327 |
liver | carcinoma | Substitution - coding silent |
c.1078T>C; p.C360R; 19:7911577-7911577 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1156C>T; p.L386L; 19:7912327-7912327 |
liver | carcinoma | Substitution - coding silent |
c.1087A>G; p.K363E; 19:7912156-7912156 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.462C>T; p.S154S; 19:7910467-7910467 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.870delC; p.P292fs*119; 19:7911264-7911264 |
NS | malignant_melanoma | Deletion - Frameshift |
c.870delC; p.P292fs*119; 19:7911264-7911264 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.569C>T; p.T190M; 19:7910697-7910697 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.275_276insTT; p.D93fs*9; 19:7910071-7910072 |
breast | carcinoma | Insertion - Frameshift |
c.1055A>G; p.D352G; 19:7911554-7911554 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.447+2T>C; p.?; 19:7910375-7910375 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.1193T>C; p.M398T; 19:7912364-7912364 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.83_84insC; p.D29fs*63; 19:7904027-7904028 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.215G>A; p.R72H; 19:7909845-7909845 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.386G>A; p.G129D; 19:7910312-7910312 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1037A>C; p.H346P; 19:7911536-7911536 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1126-2A>G; p.?; 19:7912295-7912295 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.1149C>T; p.Y383Y; 19:7912320-7912320 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.124+1G>A; p.?; 19:7904069-7904069 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.1080-1G>C; p.?; 19:7912148-7912148 |
oesophagus | carcinoma; adenocarcinoma | Unknown |
c.1173G>A; p.A391A; 19:7912344-7912344 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.90C>G; p.L30L; 19:7904034-7904034 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1063T>C; p.S355P; 19:7911562-7911562 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.690G>T; p.L230L; 19:7910994-7910994 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.827G>A; p.R276Q; 19:7911131-7911131 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1050delG; p.D352fs*59; 19:7911549-7911549 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.727G>T; p.D243Y; 19:7911031-7911031 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1196C>T; p.A399V; 19:7912367-7912367 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1196C>T; p.A399V; 19:7912367-7912367 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1086T>C; p.T362T; 19:7912155-7912155 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1022C>T; p.P341L; 19:7911521-7911521 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1247C>T; p.P416L; 19:7912418-7912418 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1022C>T; p.P341L; 19:7911521-7911521 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1022C>T; p.P341L; 19:7911521-7911521 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.872C>T; p.P291L; 19:7911266-7911266 |
skin | malignant_melanoma | Substitution - Missense |
c.730G>A; p.V244I; 19:7911034-7911034 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.730G>A; p.V244I; 19:7911034-7911034 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.730G>A; p.V244I; 19:7911034-7911034 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1022C>T; p.P341L; 19:7911521-7911521 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1144C>T; p.R382C; 19:7912315-7912315 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |