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

Basic Information

Gene ID

1045

Name

CDX2

Synonymous

caudal type homeobox 2;CDX2;caudal type homeobox 2

Definition

caudal type homeo box transcription factor 2|caudal type homeobox transcription factor 2|caudal-type homeobox protein 2|homeobox protein CDX-2

Position

13q12.3

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.780G>A; p.P260P; 13:27963277-27963277

 breastcarcinomaSubstitution - coding silent

c.883T>C; p.S295P; 13:27963174-27963174

 central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.641G>A; p.R214Q; 13:27964916-27964916

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.790C>T; p.P264S; 13:27963267-27963267

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.554C>T; p.T185M; 13:27965003-27965003

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.709C>T; p.R237C; 13:27963348-27963348

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.661G>A; p.A221T; 13:27964896-27964896

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.804C>T; p.P268P; 13:27963253-27963253

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.626G>A; p.R209H; 13:27964931-27964931

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.602T>A; p.L201Q; 13:27964955-27964955

 haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; plasma_cell_myelomaSubstitution - Missense

c.709C>T; p.R237C; 13:27963348-27963348

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.871T>G; p.S291A; 13:27963186-27963186

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.916delG; p.V306fs*2; 13:27963141-27963141

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.916delG; p.V306fs*2; 13:27963141-27963141

 large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.916delG; p.V306fs*2; 13:27963141-27963141

 large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.916delG; p.V306fs*2; 13:27963141-27963141

 large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.916delG; p.V306fs*2; 13:27963141-27963141

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.916delG; p.V306fs*2; 13:27963141-27963141

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.916delG; p.V306fs*2; 13:27963141-27963141

 large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.716C>T; p.A239V; 13:27963341-27963341

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.311C>T; p.A104V; 13:27968696-27968696

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.93C>T; p.F31F; 13:27968914-27968914

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.592C>T; p.R198W; 13:27964965-27964965

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.186G>T; p.G62G; 13:27968821-27968821

 livercarcinomaSubstitution - coding silent

c.186G>T; p.G62G; 13:27968821-27968821

 livercarcinomaSubstitution - coding silent

c.478G>T; p.G160C; 13:27968529-27968529

 livercarcinomaSubstitution - Missense

c.877C>T; p.P293S; 13:27963180-27963180

 livercarcinoma; hepatocellular_carcinomaSubstitution - Missense

c.542-2A>G; p.?; 13:27965017-27965017

 lungcarcinoma; squamous_cell_carcinomaUnknown

c.757C>G; p.Q253E; 13:27963300-27963300

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.437G>T; p.G146V; 13:27968570-27968570

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.439C>A; p.P147T; 13:27968568-27968568

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.181C>T; p.P61S; 13:27968826-27968826

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.882C>A; p.G294G; 13:27963175-27963175

 lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.531C>T; p.L177L; 13:27968476-27968476

 lungcarcinoma; non_small_cell_carcinomaSubstitution - coding silent

c.862C>G; p.L288V; 13:27963195-27963195

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.52G>T; p.V18L; 13:27968955-27968955

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.426C>A; p.P142P; 13:27968581-27968581

 lung; right_lower_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.248G>T; p.G83V; 13:27968759-27968759

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.597_598GG>TT; p.L199>?; 13:27964959-27964960

 lungcarcinoma; adenocarcinomaComplex

c.106C>T; p.Q36*; 13:27968901-27968901

 oesophaguscarcinoma; adenocarcinomaSubstitution - Nonsense

c.456C>A; p.A152A; 13:27968551-27968551

 oesophaguscarcinoma; adenocarcinomaSubstitution - coding silent

c.788C>T; p.P263L; 13:27963269-27963269

 oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.219C>A; p.L73L; 13:27968788-27968788

 pancreascarcinomaSubstitution - coding silent

c.600G>A; p.E200E; 13:27964957-27964957

 skinmalignant_melanomaSubstitution - coding silent

c.483G>A; p.Q161Q; 13:27968524-27968524

 skinmalignant_melanomaSubstitution - coding silent

c.636C>T; p.T212T; 13:27964921-27964921

 skinmalignant_melanomaSubstitution - coding silent

c.93C>T; p.F31F; 13:27968914-27968914

 skinmalignant_melanomaSubstitution - coding silent

c.721G>A; p.E241K; 13:27963336-27963336

 skinmalignant_melanomaSubstitution - Missense

c.644G>A; p.R215K; 13:27964913-27964913

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.821C>A; p.P274H; 13:27963236-27963236

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.111C>T; p.Y37Y; 13:27968896-27968896

 urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - coding silent

c.111C>T; p.Y37Y; 13:27968896-27968896

 urinary_tract; bladdercarcinomaSubstitution - coding silent