General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
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Gene ID | 7481 |
Name | WNT11 |
Synonymous | wingless-type MMTV integration site family, member 11;WNT11;wingless-type MMTV integration site family, member 11 |
Definition | protein Wnt-11 |
Position | 11q13.5 |
Gene Type | protein-coding |
Mutation summary: | Mutations in domains Mutational pattern in 17 major cancer types LoF vs missense mutations All the copy number variations from COSMIC database V72 All the mutations from COSMIC database V72 |
Mutation summary in protein domains | Top |
The non-synonymous (top) and synonymous (bottom) mutational percentage for various cancers | Top |
Loss of Function mutations compare to missense mutations | Top |
The ratio of the loss-of-function mutations over missense mutations is 0.06. |
The copy number variations for various cancers | Top |
The copy number variations in 17 major cancer types: 1; Breast, 2; Central nervous system, 3; Cervix, 4; Endometrium, 5; Haematopoietic and lymphoid_tissue, 6; Kidney, 7; Large intestine, 8; Liver, 9; Lung, 10; Not specific, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary tract |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) |
Site |
Histology |
Mutation Type |
---|---|---|---|
c.924C>T; p.S308S; 11:76187206-76187206 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.783G>T; p.K261N; 11:76191671-76191671 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.361G>A; p.A121T; 11:76194803-76194803 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.255C>G; p.A85A; 11:76196547-76196547 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.748C>T; p.R250*; 11:76191706-76191706 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1028G>T; p.R343M; 11:76187102-76187102 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.888C>T; p.D296D; 11:76191566-76191566 |
thyroid | carcinoma; anaplastic_carcinoma | Substitution - coding silent |
c.380C>T; p.A127V; 11:76194784-76194784 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.967G>T; p.D323Y; 11:76187163-76187163 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.725T>G; p.L242R; 11:76191729-76191729 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.782A>C; p.K261T; 11:76191672-76191672 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.421G>A; p.G141S; 11:76194743-76194743 |
pancreas | carcinoma | Substitution - Missense |
c.1059C>T; p.C353C; 11:76187071-76187071 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.236C>A; p.A79D; 11:76196566-76196566 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.505delG; p.A169fs*8; 11:76194659-76194659 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.236C>A; p.A79D; 11:76196566-76196566 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.126G>A; p.T42T; 11:76196676-76196676 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.443C>A; p.P148H; 11:76194721-76194721 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.29delC; p.A10fs*30; 11:76206379-76206379 |
breast | carcinoma | Deletion - Frameshift |
c.876C>T; p.H292H; 11:76191578-76191578 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.661C>T; p.R221C; 11:76191793-76191793 |
skin; face | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.661C>T; p.R221C; 11:76191793-76191793 |
breast | carcinoma | Substitution - Missense |
c.661C>T; p.R221C; 11:76191793-76191793 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.661C>T; p.R221C; 11:76191793-76191793 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.256G>A; p.D86N; 11:76196546-76196546 |
stomach | carcinoma; mixed_intestinal_and_diffuse_adenocarcinoma-unclassifiable | Substitution - Missense |
c.256G>A; p.D86N; 11:76196546-76196546 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.648C>T; p.G216G; 11:76191806-76191806 |
skin | malignant_melanoma | Substitution - coding silent |
c.541_542insA; p.T181fs*7; 11:76194622-76194623 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.541_542insA; p.T181fs*7; 11:76194622-76194623 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.262C>T; p.R88C; 11:76196540-76196540 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1031G>A; p.C344Y; 11:76187099-76187099 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1031G>A; p.C344Y; 11:76187099-76187099 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.709C>G; p.L237V; 11:76191745-76191745 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1018A>C; p.T340P; 11:76187112-76187112 |
breast | carcinoma | Substitution - Missense |
c.408C>T; p.P136P; 11:76194756-76194756 |
thyroid | other; neoplasm | Substitution - coding silent |
c.408C>T; p.P136P; 11:76194756-76194756 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1031G>T; p.C344F; 11:76187099-76187099 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.221G>A; p.R74H; 11:76196581-76196581 |
pituitary; craniopharyngeal_duct | craniopharyngioma; papillary | Substitution - Missense |
c.660C>T; p.I220I; 11:76191794-76191794 |
skin | malignant_melanoma | Substitution - coding silent |
c.719G>A; p.R240Q; 11:76191735-76191735 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.605G>A; p.R202H; 11:76191849-76191849 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.912C>A; p.N304K; 11:76187218-76187218 |
soft_tissue; striated_muscle | rhabdomyosarcoma; embryonal | Substitution - Missense |
c.1041C>T; p.T347T; 11:76187089-76187089 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.912C>A; p.N304K; 11:76187218-76187218 |
soft_tissue; striated_muscle | rhabdomyosarcoma | Substitution - Missense |
c.743T>C; p.V248A; 11:76191711-76191711 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.928G>A; p.D310N; 11:76187202-76187202 |
skin | malignant_melanoma | Substitution - Missense |
c.928G>A; p.D310N; 11:76187202-76187202 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.729G>A; p.S243S; 11:76191725-76191725 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1029G>A; p.R343R; 11:76187101-76187101 |
skin | malignant_melanoma | Substitution - coding silent |
c.197T>C; p.M66T; 11:76196605-76196605 |
prostate | carcinoma | Substitution - Missense |
c.911A>G; p.N304S; 11:76187219-76187219 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.606C>T; p.R202R; 11:76191848-76191848 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.835T>A; p.S279T; 11:76191619-76191619 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.179G>A; p.R60H; 11:76196623-76196623 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.957C>A; p.N319K; 11:76187173-76187173 |
prostate | adenoma | Substitution - Missense |
c.943G>T; p.G315W; 11:76187187-76187187 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.607G>A; p.A203T; 11:76191847-76191847 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.943G>A; p.G315R; 11:76187187-76187187 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.962A>G; p.Y321C; 11:76187168-76187168 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.621G>A; p.M207I; 11:76191833-76191833 |
skin | malignant_melanoma | Substitution - Missense |
c.914G>A; p.G305E; 11:76187216-76187216 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.621G>A; p.M207I; 11:76191833-76191833 |
skin | malignant_melanoma | Substitution - Missense |
c.476A>G; p.D159G; 11:76194688-76194688 |
skin | malignant_melanoma | Substitution - Missense |
c.909C>T; p.S303S; 11:76187221-76187221 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.84G>A; p.L28L; 11:76196718-76196718 |
liver | carcinoma | Substitution - coding silent |
c.1024C>T; p.R342C; 11:76187106-76187106 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1056C>G; p.V352V; 11:76187074-76187074 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.666C>T; p.T222T; 11:76191788-76191788 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.797G>T; p.R266L; 11:76191657-76191657 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.628A>G; p.K210E; 11:76191826-76191826 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.628A>G; p.K210E; 11:76191826-76191826 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.956A>G; p.N319S; 11:76187174-76187174 |
adrenal_gland; adrenal_gland | adrenal_cortical_carcinoma; functioning | Substitution - Missense |
c.1044G>A; p.V348V; 11:76187086-76187086 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.749G>A; p.R250Q; 11:76191705-76191705 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.223G>A; p.E75K; 11:76196579-76196579 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.223G>A; p.E75K; 11:76196579-76196579 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.223G>A; p.E75K; 11:76196579-76196579 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.125C>T; p.T42M; 11:76196677-76196677 |
thyroid | carcinoma | Substitution - Missense |
c.752C>T; p.P251L; 11:76191702-76191702 |
skin | malignant_melanoma | Substitution - Missense |
c.523C>T; p.P175S; 11:76194641-76194641 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.799C>G; p.P267A; 11:76191655-76191655 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.56C>T; p.T19I; 11:76206352-76206352 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.667T>A; p.C223S; 11:76191787-76191787 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1052A>G; p.Y351C; 11:76187078-76187078 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |