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

Basic Information

Gene ID

7913

Name

DEK

Synonymous

DEK proto-oncogene;DEK;DEK proto-oncogene

Definition

DEK oncogene (DNA binding)|protein DEK

Position

6p22.3

Gene Type

protein-coding

COSMIC confirmed somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.904G>A; p.E302K; 6:18236595-18236595

breastcarcinomaSubstitution - Missense

c.70G>A; p.E24K; 6:18263918-18263918

breastcarcinomaSubstitution - Missense

c.700G>A; p.E234K; 6:18249713-18249713

breastcarcinomaSubstitution - Missense

c.926A>C; p.D309A; 6:18236573-18236573

central_nervous_system; braingliomaSubstitution - Missense

c.412G>T; p.G138*; 6:18256401-18256401

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.750A>C; p.E250D; 6:18249663-18249663

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.756A>C; p.E252D; 6:18249657-18249657

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.863G>C; p.S288T; 6:18237416-18237416

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.987A>G; p.I329M; 6:18236512-18236512

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1090G>T; p.D364Y; 6:18226200-18226200

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1068T>G; p.T356T; 6:18226222-18226222

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.1044A>T; p.K348N; 6:18236455-18236455

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.291delT; p.L98fs*1; 6:18258019-18258019

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.997C>T; p.L333L; 6:18236502-18236502

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.412G>T; p.G138*; 6:18256401-18256401

large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.412G>T; p.G138*; 6:18256401-18256401

large_intestine; coloncarcinomaSubstitution - Nonsense

c.452delA; p.K151fs*7; 6:18256361-18256361

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.476G>A; p.S159N; 6:18255828-18255828

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.582G>A; p.P194P; 6:18249831-18249831

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.524T>G; p.L175R; 6:18255780-18255780

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.595delA; p.T199fs*79; 6:18249818-18249818

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.862A>G; p.S288G; 6:18237417-18237417

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.309C>T; p.T103T; 6:18258001-18258001

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.862A>G; p.S288G; 6:18237417-18237417

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1043A>G; p.K348R; 6:18236456-18236456

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.605A>G; p.K202R; 6:18249808-18249808

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1043A>G; p.K348R; 6:18236456-18236456

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.950A>G; p.K317R; 6:18236549-18236549

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.411delA; p.G138fs*12; 6:18256402-18256402

large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.39C>A; p.T13T; 6:18263949-18263949

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.506C>T; p.S169L; 6:18255798-18255798

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.506C>T; p.S169L; 6:18255798-18255798

large_intestine; coloncarcinomaSubstitution - Missense

c.506C>T; p.S169L; 6:18255798-18255798

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.1042A>G; p.K348E; 6:18236457-18236457

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.151A>G; p.S51G; 6:18258400-18258400

livercarcinomaSubstitution - Missense

c.151A>G; p.S51G; 6:18258400-18258400

livercarcinomaSubstitution - Missense

c.1027A>G; p.M343V; 6:18236472-18236472

livercarcinomaSubstitution - Missense

c.358G>T; p.V120L; 6:18256455-18256455

livercarcinomaSubstitution - Missense

c.908C>G; p.S303C; 6:18236591-18236591

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.190G>T; p.E64*; 6:18258361-18258361

lungcarcinoma; adenocarcinomaSubstitution - Nonsense

c.607G>T; p.G203C; 6:18249806-18249806

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.224G>C; p.R75T; 6:18258327-18258327

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.26A>C; p.E9A; 6:18263962-18263962

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.78C>A; p.P26P; 6:18263910-18263910

oesophaguscarcinoma; adenocarcinomaSubstitution - coding silent

c.17C>G; p.P6R; 6:18263971-18263971

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.452+2T>G; p.?; 6:18256359-18256359

pancreascarcinomaUnknown

c.232T>G; p.F78V; 6:18258319-18258319

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.279G>A; p.R93R; 6:18258031-18258031

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.422A>T; p.Q141L; 6:18256391-18256391

skinmalignant_melanomaSubstitution - Missense

c.123G>C; p.E41D; 6:18263865-18263865

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.123G>C; p.E41D; 6:18263865-18263865

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.123G>C; p.E41D; 6:18263865-18263865

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.154C>T; p.L52F; 6:18258397-18258397

skinmalignant_melanomaSubstitution - Missense

c.276G>C; p.E92D; 6:18258034-18258034

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.248-7_248-6insT; p.?; 6:18258068-18258069

stomachcarcinoma; diffuse_adenocarcinomaUnknown

c.632C>A; p.S211Y; 6:18249781-18249781

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.503G>C; p.R168T; 6:18255801-18255801

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.863G>C; p.S288T; 6:18237416-18237416

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.358G>A; p.V120M; 6:18256455-18256455

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.9C>T; p.A3A; 6:18263979-18263979

thyroidother; neoplasmSubstitution - coding silent

c.710A>G; p.K237R; 6:18249703-18249703

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.25G>A; p.E9K; 6:18263963-18263963

urinary_tract; bladdercarcinomaSubstitution - Missense

c.533G>C; p.R178T; 6:18255771-18255771

urinary_tract; bladdercarcinomaSubstitution - Missense

c.742G>C; p.D248H; 6:18249671-18249671

urinary_tract; bladdercarcinomaSubstitution - Missense