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

Basic Information

Gene ID

3934

Name

LCN2

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.339G>A; p.T113T; 9:128151701-128151701

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.77A>G; p.D26G; 9:128149602-128149602

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.5C>G; p.P2R; 9:128149530-128149530

 pancreascarcinomaSubstitution - Missense

c.276G>A; p.R92R; 9:128151638-128151638

 skinmalignant_melanomaSubstitution - coding silent

c.381C>T; p.L127L; 9:128151931-128151931

 urinary_tract; bladdercarcinomaSubstitution - coding silent

c.71C>T; p.T24I; 9:128149596-128149596

 pancreascarcinomaSubstitution - Missense

c.138+1G>A; p.?; 9:128149664-128149664

 urinary_tract; bladdercarcinomaUnknown

c.502C>G; p.L168V; 9:128152209-128152209

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.571C>T; p.P191S; 9:128152278-128152278

 skin; facecarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.459C>G; p.F153L; 9:128152009-128152009

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.574A>G; p.I192V; 9:128152281-128152281

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.327C>T; p.P109P; 9:128151689-128151689

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.469C>A; p.L157I; 9:128152019-128152019

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.589G>A; p.D197N; 9:128153111-128153111

 skinmalignant_melanomaSubstitution - Missense

c.64G>T; p.D22Y; 9:128149589-128149589

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.591C>T; p.D197D; 9:128153113-128153113

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.497C>T; p.S166L; 9:128152204-128152204

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.69C>T; p.S23S; 9:128149594-128149594

 skinmalignant_melanomaSubstitution - coding silent

c.80T>C; p.L27P; 9:128149605-128149605

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.291C>A; p.D97E; 9:128151653-128151653

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.138+5G>A; p.?; 9:128149668-128149668

 central_nervous_system; cerebellumprimitive_neuroectodermal_tumour-medulloblastoma; SHH_subtypeUnknown

c.138+5G>A; p.?; 9:128149668-128149668

 central_nervous_system; brainprimitive_neuroectodermal_tumour-medulloblastoma; medullomyoblastomaUnknown

c.558C>T; p.I186I; 9:128152265-128152265

 skinmalignant_melanomaSubstitution - coding silent

c.204G>A; p.P68P; 9:128150303-128150303

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.204G>A; p.P68P; 9:128150303-128150303

 large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.79C>A; p.L27M; 9:128149604-128149604

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.79C>A; p.L27M; 9:128149604-128149604

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.287G>A; p.C96Y; 9:128151649-128151649

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.474C>T; p.Y158Y; 9:128152024-128152024

 stomachadenocarcinomaSubstitution - coding silent

c.557T>A; p.I186N; 9:128152264-128152264

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.564_565CC>TT; p.P189S; 9:128152271-128152272

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.557T>A; p.I186N; 9:128152264-128152264

 upper_aerodigestive_tract; mouthcarcinomaSubstitution - Missense

c.270G>T; p.L90L; 9:128150369-128150369

 oesophagus; middle_thirdcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.330C>G; p.G110G; 9:128151692-128151692

 breastcarcinomaSubstitution - coding silent

c.448A>T; p.R150W; 9:128151998-128151998

 oesophaguscarcinomaSubstitution - Missense

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