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Gene information | Literature | Expression | lncRNA | Mutation | Homolog

Basic Information

Gene ID

4005

Name

LMO2

Synonymous

LIM domain only 2 (rhombotin-like 1);LMO2;LIM domain only 2 (rhombotin-like 1)

Definition

LIM domain only protein 2|LMO-2|T-cell translocation gene 2|T-cell translocation protein 2|cysteine-rich protein TTG-2|rhombotin 2|rhombotin-2|rhombotin-like 1

Position

11p13

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.241C>T; p.R81W; 11:33864618-33864618

 breastcarcinomaSubstitution - Missense

c.237C>T; p.L79L; 11:33864622-33864622

 breastcarcinomaSubstitution - coding silent

c.289T>C; p.C97R; 11:33859544-33859544

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.303T>G; p.I101M; 11:33859530-33859530

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.315G>T; p.E105D; 11:33859518-33859518

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.394G>T; p.G132C; 11:33859439-33859439

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.105G>T; p.Q35H; 11:33864754-33864754

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.473T>C; p.I158T; 11:33859360-33859360

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.111T>C; p.I37I; 11:33864748-33864748

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.111T>C; p.I37I; 11:33864748-33864748

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.433G>A; p.E145K; 11:33859400-33859400

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.259C>T; p.L87F; 11:33859574-33859574

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.298C>T; p.R100W; 11:33859535-33859535

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.273C>T; p.D91D; 11:33859560-33859560

 livercarcinomaSubstitution - coding silent

c.72C>T; p.P24P; 11:33864787-33864787

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.206G>T; p.R69L; 11:33864653-33864653

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.394_395GG>TT; p.G132>?; 11:33859438-33859439

 lungcarcinoma; adenocarcinomaComplex

c.259C>T; p.L87F; 11:33859574-33859574

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.96C>T; p.G32G; 11:33864763-33864763

 lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.440A>T; p.D147V; 11:33859393-33859393

 NSNSSubstitution - Missense

c.171C>T; p.C57C; 11:33864688-33864688

 oesophaguscarcinoma; adenocarcinomaSubstitution - coding silent

c.257G>C; p.R86T; 11:33864602-33864602

 pancreascarcinomaSubstitution - Missense

c.432C>T; p.C144C; 11:33859401-33859401

 pleurapulmonary_blastomaSubstitution - coding silent

c.168C>T; p.S56S; 11:33864691-33864691

 prostatecarcinoma; adenocarcinomaSubstitution - coding silent

c.361A>G; p.K121E; 11:33859472-33859472

 prostatecarcinomaSubstitution - Missense

c.72C>T; p.P24P; 11:33864787-33864787

 skinmalignant_melanomaSubstitution - coding silent

c.433G>A; p.E145K; 11:33859400-33859400

 skinmalignant_melanomaSubstitution - Missense

c.71C>T; p.P24L; 11:33864788-33864788

 skinmalignant_melanomaSubstitution - Missense

c.230G>A; p.R77Q; 11:33864629-33864629

 skinmalignant_melanomaSubstitution - Missense

c.438G>A; p.Q146Q; 11:33859395-33859395

 skinmalignant_melanomaSubstitution - coding silent

c.311A>C; p.Y104S; 11:33859522-33859522

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.371C>T; p.A124V; 11:33859462-33859462

 skinmalignant_melanomaSubstitution - Missense

c.439G>A; p.D147N; 11:33859394-33859394

 skinmalignant_melanomaSubstitution - Missense

c.304C>T; p.R102C; 11:33859529-33859529

 skinmalignant_melanomaSubstitution - Missense

c.304C>T; p.R102C; 11:33859529-33859529

 skinmalignant_melanomaSubstitution - Missense

c.388T>G; p.C130G; 11:33859445-33859445

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.363A>G; p.K121K; 11:33859470-33859470

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.370G>A; p.A124T; 11:33859463-33859463

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.305G>A; p.R102H; 11:33859528-33859528

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.172G>T; p.D58Y; 11:33864687-33864687

 stomachcarcinoma; mixed_intestinal_and_diffuse_adenocarcinoma-unclassifiableSubstitution - Missense

c.242G>A; p.R81Q; 11:33864617-33864617

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.366C>T; p.C122C; 11:33859467-33859467

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.111T>C; p.I37I; 11:33864748-33864748

 thyroidother; neoplasmSubstitution - coding silent

c.325C>T; p.R109W; 11:33859508-33859508

 upper_aerodigestive_tract; mouthcarcinomaSubstitution - Missense

c.325C>T; p.R109W; 11:33859508-33859508

 upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.99C>A; p.C33*; 11:33864760-33864760

 urinary_tract; bladdercarcinomaSubstitution - Nonsense