Epithelial-Mesenchymal Transition gene database (dbEMT) Home
dbEMT
dbEMT 2.0
General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

7702

Name

ZNF143

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.1293G>A; p.T431T; 11:9508764-9508764

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.1324G>A; p.D442N; 11:9508795-9508795

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.1008G>T; p.R336R; 11:9501131-9501131

urinary_tract; bladdercarcinomaSubstitution - coding silent

c.1440C>T; p.D480D; 11:9512512-9512512

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.146G>T; p.S49I; 11:9472710-9472710

thyroidother; neoplasmSubstitution - Missense

c.1291A>G; p.T431A; 11:9508762-9508762

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.299G>T; p.S100I; 11:9474559-9474559

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.840A>G; p.T280T; 11:9496377-9496377

skinmalignant_melanomaSubstitution - coding silent

c.870T>G; p.T290T; 11:9497703-9497703

kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - coding silent

c.480T>G; p.I160M; 11:9478496-9478496

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.702G>C; p.E234D; 11:9494702-9494702

breastcarcinomaSubstitution - Missense

c.1234A>G; p.T412A; 11:9508705-9508705

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1589G>T; p.G530V; 11:9516265-9516265

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1608C>T; p.P536P; 11:9516284-9516284

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.1296G>A; p.L432L; 11:9508767-9508767

prostateadenomaSubstitution - coding silent

c.1608C>T; p.P536P; 11:9516284-9516284

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.401C>T; p.A134V; 11:9478417-9478417

central_nervous_system; braingliomaSubstitution - Missense

c.105C>T; p.T35T; 11:9471413-9471413

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.1554C>T; p.A518A; 11:9516230-9516230

skinmalignant_melanomaSubstitution - coding silent

c.1064G>A; p.R355K; 11:9501187-9501187

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1413G>A; p.T471T; 11:9512485-9512485

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.1413G>A; p.T471T; 11:9512485-9512485

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.892C>T; p.R298W; 11:9497725-9497725

skinmalignant_melanomaSubstitution - Missense

c.1041C>T; p.H347H; 11:9501164-9501164

central_nervous_system; braingliomaSubstitution - coding silent

c.1798G>A; p.V600I; 11:9525351-9525351

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.847G>A; p.G283R; 11:9497680-9497680

oesophagus; middle_thirdcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.402G>A; p.A134A; 11:9478418-9478418

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1217A>C; p.K406T; 11:9508688-9508688

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.187A>C; p.I63L; 11:9472751-9472751

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.856A>C; p.S286R; 11:9497689-9497689

kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

c.132T>C; p.N44N; 11:9472696-9472696

skinmalignant_melanomaSubstitution - coding silent

c.824G>A; p.G275E; 11:9496361-9496361

skin; extremitymalignant_melanomaSubstitution - Missense

c.1192T>C; p.F398L; 11:9508663-9508663

salivary_glandcarcinoma; adenoid_cystic_carcinomaSubstitution - Missense

c.858T>A; p.S286R; 11:9497691-9497691

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; essential_thrombocythaemiaSubstitution - Missense

c.1475C>G; p.S492C; 11:9512547-9512547

ovaryother; neoplasmSubstitution - Missense

c.1475C>G; p.S492C; 11:9512547-9512547

ovaryother; neoplasmSubstitution - Missense

c.1611C>G; p.A537A; 11:9516287-9516287

boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.1086A>G; p.P362P; 11:9501209-9501209

livercarcinomaSubstitution - coding silent

c.1086A>G; p.P362P; 11:9501209-9501209

livercarcinomaSubstitution - coding silent

c.192A>G; p.Q64Q; 11:9472756-9472756

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.192A>G; p.Q64Q; 11:9472756-9472756

breastcarcinomaSubstitution - coding silent

c.585A>G; p.G195G; 11:9479486-9479486

breastcarcinomaSubstitution - coding silent

c.169G>A; p.D57N; 11:9472733-9472733

skinmalignant_melanomaSubstitution - Missense

c.1833+3G>A; p.?; 11:9525389-9525389

breastcarcinomaUnknown

c.1641G>A; p.T547T; 11:9516317-9516317

lungcarcinoma; small_cell_carcinomaSubstitution - coding silent

c.1533A>G; p.I511M; 11:9516209-9516209

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.1814G>A; p.G605D; 11:9525367-9525367

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_leukaemiaSubstitution - Missense

c.1141C>T; p.H381Y; 11:9501264-9501264

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1309C>T; p.R437W; 11:9508780-9508780

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.1610C>T; p.A537V; 11:9516286-9516286

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1698A>G; p.V566V; 11:9525251-9525251

boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - coding silent

c.901G>A; p.E301K; 11:9497734-9497734

skin; extremitymalignant_melanomaSubstitution - Missense

c.994G>A; p.E332K; 11:9501117-9501117

oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.1740G>A; p.M580I; 11:9525293-9525293

skinmalignant_melanomaSubstitution - Missense

c.349G>T; p.A117S; 11:9474609-9474609

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1505C>A; p.S502Y; 11:9512577-9512577

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1089A>C; p.G363G; 11:9501212-9501212

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1230C>T; p.V410V; 11:9508701-9508701

skinmalignant_melanomaSubstitution - coding silent

c.157G>A; p.V53I; 11:9472721-9472721

breastcarcinomaSubstitution - Missense

c.22C>T; p.R8*; 11:9471330-9471330

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Nonsense

c.794G>A; p.R265Q; 11:9496331-9496331

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.112+2T>C; p.?; 11:9471422-9471422

stomachcarcinoma; adenocarcinomaUnknown

c.993C>T; p.F331F; 11:9501116-9501116

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1724C>G; p.T575S; 11:9525277-9525277

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1190G>T; p.R397M; 11:9508661-9508661

pancreascarcinomaSubstitution - Missense

c.29C>A; p.S10Y; 11:9471337-9471337

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.188T>C; p.I63T; 11:9472752-9472752

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1584G>A; p.Q528Q; 11:9516260-9516260

skinmalignant_melanomaSubstitution - coding silent

c.1696G>C; p.V566L; 11:9525249-9525249

boneEwings_sarcoma-peripheral_primitive_neuroectodermal_tumourSubstitution - Missense

c.653T>C; p.L218S; 11:9494653-9494653

breastcarcinomaSubstitution - Missense

c.280C>A; p.P94T; 11:9474015-9474015

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.50C>T; p.P17L; 11:9471358-9471358

skinmalignant_melanomaSubstitution - Missense

c.712C>T; p.R238*; 11:9494712-9494712

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.712C>T; p.R238*; 11:9494712-9494712

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.712C>T; p.R238*; 11:9494712-9494712

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.1459G>A; p.A487T; 11:9512531-9512531

skinmalignant_melanomaSubstitution - Missense

c.1050A>G; p.T350T; 11:9501173-9501173

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.1042G>A; p.V348I; 11:9501165-9501165

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.1029C>T; p.I343I; 11:9501152-9501152

skinmalignant_melanomaSubstitution - coding silent

c.68C>T; p.A23V; 11:9471376-9471376

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.68C>T; p.A23V; 11:9471376-9471376

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.1146A>G; p.T382T; 11:9501269-9501269

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.899C>T; p.S300L; 11:9497732-9497732

skinmalignant_melanomaSubstitution - Missense

c.1401G>T; p.G467G; 11:9512473-9512473

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.1340A>C; p.E447A; 11:9508811-9508811

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1338C>T; p.I446I; 11:9508809-9508809

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.945G>T; p.Q315H; 11:9497778-9497778

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.294G>A; p.G98G; 11:9474554-9474554

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.23G>A; p.R8Q; 11:9471331-9471331

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.757C>T; p.H253Y; 11:9494757-9494757

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense


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