| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 7088 |
Name | TLE1 |
Synonymous | transducin-like enhancer of split 1 (E(sp1) homolog, Drosophila);TLE1;transducin-like enhancer of split 1 (E(sp1) homolog, Drosophila) |
Definition | enhancer of split groucho-like protein 1|transducin-like enhancer protein 1 |
Position | 9q21.32 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.225G>T; p.M75I; 9:81685685-81685685 |
adrenal_gland; adrenal_gland | adrenal_cortical_carcinoma; functioning | Substitution - Missense |
c.1464C>G; p.C488W; 9:81593142-81593142 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.2230_2234delAGCTG; p.S744fs*1; 9:81584277-81584281 |
biliary_tract; bile_duct | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1212A>G; p.A404A; 9:81611811-81611811 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1830G>T; p.R610S; 9:81587828-81587828 |
breast | carcinoma | Substitution - Missense |
c.1846A>G; p.T616A; 9:81587812-81587812 |
breast | carcinoma | Substitution - Missense |
c.1852G>C; p.G618R; 9:81587806-81587806 |
breast | carcinoma | Substitution - Missense |
c.686T>G; p.V229G; 9:81620466-81620466 |
breast | carcinoma | Substitution - Missense |
c.2004C>T; p.T668T; 9:81585629-81585629 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.2004C>T; p.T668T; 9:81585629-81585629 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.1980C>A; p.I660I; 9:81585653-81585653 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.579_582delCAGA; p.D193fs*15; 9:81633360-81633363 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - Frameshift |
c.2176C>T; p.R726W; 9:81584477-81584477 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1917_1937del21; p.V640_R646delVRSWDLR; 9:81587721-81587741 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - In frame |
c.1707G>T; p.E569D; 9:81590927-81590927 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1852G>A; p.G618R; 9:81587806-81587806 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1898C>T; p.T633M; 9:81587760-81587760 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.907G>T; p.E303*; 9:81615993-81615993 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.907G>T; p.E303*; 9:81615993-81615993 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.2299G>T; p.E767*; 9:81584212-81584212 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.623_624insTT; p.R209fs*1; 9:81620528-81620529 |
endometrium | carcinoma; endometrioid_carcinoma | Insertion - Frameshift |
c.2164_2166delCTC; p.L722delL; 9:81584487-81584489 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - In frame |
c.1938C>T; p.R646R; 9:81587720-81587720 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.829C>T; p.R277C; 9:81616071-81616071 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1225G>A; p.A409T; 9:81611798-81611798 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1600C>T; p.R534C; 9:81591034-81591034 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1899G>T; p.T633T; 9:81587759-81587759 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.1117G>T; p.G373W; 9:81611906-81611906 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.2183_2184insT; p.Y729fs*16; 9:81584469-81584470 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Insertion - Frameshift |
c.1062G>A; p.A354A; 9:81613378-81613378 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemia | Substitution - coding silent |
c.63T>C; p.T21T; 9:81687396-81687396 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.2119G>A; p.A707T; 9:81585514-81585514 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1726G>A; p.A576T; 9:81590908-81590908 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.304C>G; p.Q102E; 9:81652282-81652282 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.357G>C; p.L119F; 9:81652229-81652229 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.2100C>T; p.C700C; 9:81585533-81585533 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.468G>A; p.P156P; 9:81634206-81634206 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1660T>G; p.L554V; 9:81590974-81590974 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1326G>A; p.G442G; 9:81610225-81610225 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1679C>T; p.A560V; 9:81590955-81590955 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.119A>G; p.Y40C; 9:81687340-81687340 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1324G>A; p.G442R; 9:81610227-81610227 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1852G>C; p.G618R; 9:81587806-81587806 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1274delC; p.P425fs*3; 9:81610277-81610277 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1215C>A; p.A405A; 9:81611808-81611808 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1465G>A; p.A489T; 9:81593141-81593141 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1741G>A; p.A581T; 9:81590893-81590893 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1741G>A; p.A581T; 9:81590893-81590893 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1741G>A; p.A581T; 9:81590893-81590893 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1407C>T; p.P469P; 9:81593199-81593199 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.109C>A; p.Q37K; 9:81687350-81687350 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1690C>T; p.P564S; 9:81590944-81590944 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.997G>A; p.A333T; 9:81613443-81613443 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1593T>C; p.N531N; 9:81591041-81591041 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1165G>A; p.A389T; 9:81611858-81611858 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.234+2T>C; p.?; 9:81685674-81685674 |
large_intestine; caecum | carcinoma; adenocarcinoma | Unknown |
c.1680G>A; p.A560A; 9:81590954-81590954 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1852G>T; p.G618*; 9:81587806-81587806 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1693C>T; p.R565C; 9:81590941-81590941 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1693C>T; p.R565C; 9:81590941-81590941 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.195T>C; p.Y65Y; 9:81685715-81685715 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2085C>T; p.H695H; 9:81585548-81585548 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1291A>G; p.T431A; 9:81610260-81610260 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1595A>C; p.Y532S; 9:81591039-81591039 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.1239C>T; p.Y413Y; 9:81611784-81611784 |
liver | carcinoma | Substitution - coding silent |
c.1854A>T; p.G618G; 9:81587804-81587804 |
liver | carcinoma | Substitution - coding silent |
c.1854A>T; p.G618G; 9:81587804-81587804 |
liver | carcinoma | Substitution - coding silent |
c.1527C>G; p.V509V; 9:81593079-81593079 |
liver | carcinoma | Substitution - coding silent |
c.1402G>T; p.G468*; 9:81593204-81593204 |
liver | carcinoma | Substitution - Nonsense |
c.1390G>A; p.D464N; 9:81593216-81593216 |
liver | carcinoma | Substitution - Missense |
c.1390G>A; p.D464N; 9:81593216-81593216 |
liver | carcinoma | Substitution - Missense |
c.1857_1860delCAGC; p.S620fs*66; 9:81587798-81587801 |
liver | carcinoma | Deletion - Frameshift |
c.1561G>T; p.V521F; 9:81593045-81593045 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.665A>G; p.N222S; 9:81620487-81620487 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1534A>T; p.I512F; 9:81593072-81593072 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1848A>G; p.T616T; 9:81587810-81587810 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1459G>A; p.V487M; 9:81593147-81593147 |
lung; middle_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.664A>G; p.N222D; 9:81620488-81620488 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.294G>A; p.Q98Q; 9:81653977-81653977 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.526C>T; p.H176Y; 9:81634148-81634148 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2260A>G; p.I754V; 9:81584251-81584251 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1852G>C; p.G618R; 9:81587806-81587806 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1427G>T; p.R476L; 9:81593179-81593179 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1402G>T; p.G468*; 9:81593204-81593204 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.975C>T; p.D325D; 9:81613465-81613465 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2110C>T; p.L704L; 9:81585523-81585523 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1796C>A; p.A599D; 9:81590838-81590838 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.712G>T; p.D238Y; 9:81616699-81616699 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.2207C>G; p.S736C; 9:81584304-81584304 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.347T>A; p.M116K; 9:81652239-81652239 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.581G>C; p.R194T; 9:81633361-81633361 |
NS | NS | Substitution - Missense |
c.203C>T; p.S68L; 9:81685707-81685707 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.657A>G; p.E219E; 9:81620495-81620495 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1558C>G; p.P520A; 9:81593048-81593048 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1829+4A>G; p.?; 9:81590801-81590801 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Unknown |
c.1713G>A; p.T571T; 9:81590921-81590921 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1427G>A; p.R476H; 9:81593179-81593179 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.2057T>A; p.V686E; 9:81585576-81585576 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1243C>T; p.R415C; 9:81611780-81611780 |
pancreas | carcinoma | Substitution - Missense |
c.764A>C; p.E255A; 9:81616647-81616647 |
pancreas | carcinoma | Substitution - Missense |
c.764A>C; p.E255A; 9:81616647-81616647 |
pancreas | carcinoma; ductal_carcinoma | Substitution - Missense |
c.1359C>G; p.D453E; 9:81593247-81593247 |
pleura | pulmonary_blastoma | Substitution - Missense |
c.1896G>C; p.W632C; 9:81587762-81587762 |
prostate | carcinoma | Substitution - Missense |
c.1017A>G; p.P339P; 9:81613423-81613423 |
prostate | carcinoma | Substitution - coding silent |
c.2258A>G; p.Y753C; 9:81584253-81584253 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.2108C>T; p.S703F; 9:81585525-81585525 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.121C>T; p.H41Y; 9:81687338-81687338 |
skin | malignant_melanoma | Substitution - Missense |
c.2188G>A; p.G730R; 9:81584465-81584465 |
skin; hand | malignant_melanoma | Substitution - Missense |
c.603C>T; p.S201S; 9:81620549-81620549 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.741C>T; p.N247N; 9:81616670-81616670 |
skin | malignant_melanoma | Substitution - coding silent |
c.242T>A; p.I81N; 9:81654029-81654029 |
skin | malignant_melanoma | Substitution - Missense |
c.1012C>T; p.R338C; 9:81613428-81613428 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.662C>T; p.S221F; 9:81620490-81620490 |
skin | malignant_melanoma | Substitution - Missense |
c.1119delG; p.M374fs*7; 9:81611904-81611904 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Deletion - Frameshift |
c.427C>T; p.L143F; 9:81634247-81634247 |
skin | malignant_melanoma | Substitution - Missense |
c.1203G>A; p.M401I; 9:81611820-81611820 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1129delC; p.H377fs*4; 9:81611894-81611894 |
skin | malignant_melanoma | Deletion - Frameshift |
c.493C>T; p.L165F; 9:81634181-81634181 |
skin | malignant_melanoma | Substitution - Missense |
c.2182C>T; p.P728S; 9:81584471-81584471 |
skin; face | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1646G>A; p.G549E; 9:81590988-81590988 |
skin; scalp | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1386C>T; p.P462P; 9:81593220-81593220 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1407C>T; p.P469P; 9:81593199-81593199 |
skin | malignant_melanoma | Substitution - coding silent |
c.1250C>T; p.P417L; 9:81611773-81611773 |
skin | malignant_melanoma | Substitution - Missense |
c.829C>T; p.R277C; 9:81616071-81616071 |
skin | malignant_melanoma | Substitution - Missense |
c.1276C>T; p.H426Y; 9:81610275-81610275 |
skin | malignant_melanoma | Substitution - Missense |
c.1112C>T; p.P371L; 9:81611911-81611911 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1112_1113delCT; p.P371fs*51; 9:81611910-81611911 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Deletion - Frameshift |
c.467C>T; p.P156L; 9:81634207-81634207 |
soft_tissue; blood_vessel | angiosarcoma | Substitution - Missense |
c.1501A>G; p.T501A; 9:81593105-81593105 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1326G>A; p.G442G; 9:81610225-81610225 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.908A>G; p.E303G; 9:81615992-81615992 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1159C>A; p.P387T; 9:81611864-81611864 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.144G>C; p.E48D; 9:81685878-81685878 |
stomach | carcinoma; mixed_intestinal_and_diffuse_adenocarcinoma-unclassifiable | Substitution - Missense |
c.1131C>T; p.H377H; 9:81611892-81611892 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2231G>A; p.S744N; 9:81584280-81584280 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2219C>T; p.S740L; 9:81584292-81584292 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1734C>T; p.Y578Y; 9:81590900-81590900 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1165G>A; p.A389T; 9:81611858-81611858 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.590G>A; p.G197D; 9:81633352-81633352 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.2170G>C; p.A724P; 9:81584483-81584483 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.957A>T; p.T319T; 9:81613483-81613483 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.2212G>C; p.E738Q; 9:81584299-81584299 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.2212G>C; p.E738Q; 9:81584299-81584299 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.201G>T; p.M67I; 9:81685709-81685709 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1874C>G; p.S625C; 9:81587784-81587784 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.859C>G; p.P287A; 9:81616041-81616041 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.871G>A; p.A291T; 9:81616029-81616029 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.622C>T; p.L208L; 9:81620530-81620530 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |