Cancer metastasis gene database Home
Cancer metastasis database
General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction

Basic Information

Gene ID

51201

Name

ZDHHC2

Synonymous

zinc finger, DHHC-type containing 2;ZDHHC2;zinc finger, DHHC-type containing 2

Definition

DHHC-2|palmitoyltransferase ZDHHC2|ream|rec|reduced expression associated with metastasis protein|reduced expression in cancer protein|zinc finger DHHC domain-containing protein 2|zinc finger protein 372|zinc finger, DHHC domain containing 2

Position

8p22

Gene Type

protein-coding

COSMIC somatic mutation   [Top]

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.328C>T; p.R110*; 8:17195579-17195579

large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.380G>A; p.R127Q; 8:17197588-17197588

skinmalignant_melanomaSubstitution - Missense

c.805C>T; p.R269*; 8:17210006-17210006

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.466C>T; p.H156Y; 8:17198403-17198403

skinmalignant_melanomaSubstitution - Missense

c.764C>T; p.T255I; 8:17209965-17209965

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.139G>A; p.E47K; 8:17184797-17184797

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1053A>G; p.K351K; 8:17215339-17215339

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.1053A>G; p.K351K; 8:17215339-17215339

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - coding silent

c.941C>A; p.T314K; 8:17210471-17210471

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.576G>A; p.Q192Q; 8:17205754-17205754

breastcarcinomaSubstitution - coding silent

c.227C>T; p.T76I; 8:17186400-17186400

stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.500C>T; p.S167L; 8:17205678-17205678

skinmalignant_melanomaSubstitution - Missense

c.364A>G; p.M122V; 8:17195615-17195615

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.5C>T; p.A2V; 8:17156728-17156728

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.315G>A; p.Q105Q; 8:17195566-17195566

skinmalignant_melanomaSubstitution - coding silent

c.812delT; p.F272fs*16; 8:17210013-17210013

stomachcarcinoma; intestinal_adenocarcinomaDeletion - Frameshift

c.970C>T; p.P324S; 8:17215256-17215256

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.970C>T; p.P324S; 8:17215256-17215256

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.415C>T; p.R139C; 8:17197623-17197623

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.730+10C>T; p.?; 8:17208102-17208102

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaUnknown

c.432C>T; p.S144S; 8:17197640-17197640

skinmalignant_melanomaSubstitution - coding silent

c.460G>T; p.D154Y; 8:17198397-17198397

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.904C>T; p.P302S; 8:17210434-17210434

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.978G>A; p.K326K; 8:17215264-17215264

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.339G>A; p.K113K; 8:17195590-17195590

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.828G>A; p.K276K; 8:17210029-17210029

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.618A>C; p.Q206H; 8:17207980-17207980

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.710G>T; p.S237I; 8:17208072-17208072

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.519C>A; p.L173L; 8:17205697-17205697

skinmalignant_melanomaSubstitution - coding silent

c.880C>T; p.P294S; 8:17210410-17210410

skinmalignant_melanomaSubstitution - Missense

c.806G>A; p.R269Q; 8:17210007-17210007

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.809A>C; p.Q270P; 8:17210010-17210010

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.585C>T; p.I195I; 8:17205763-17205763

skinmalignant_melanomaSubstitution - coding silent

c.907G>A; p.E303K; 8:17210437-17210437

breastcarcinomaSubstitution - Missense

c.498T>G; p.F166L; 8:17205676-17205676

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.368C>G; p.S123C; 8:17195619-17195619

skinmalignant_melanomaSubstitution - Missense

c.417C>A; p.R139R; 8:17197625-17197625

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.951-2A>G; p.?; 8:17215235-17215235

large_intestine; caecumcarcinoma; adenocarcinomaUnknown

c.331G>A; p.A111T; 8:17195582-17195582

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.50T>G; p.V17G; 8:17156773-17156773

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.50T>G; p.V17G; 8:17156773-17156773

thyroidother; neoplasmSubstitution - Missense

c.50T>G; p.V17G; 8:17156773-17156773

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.50T>G; p.V17G; 8:17156773-17156773

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.50T>G; p.V17G; 8:17156773-17156773

upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.754C>T; p.R252*; 8:17209955-17209955

skinmalignant_melanomaSubstitution - Nonsense

c.857+7C>T; p.?; 8:17210065-17210065

stomachcarcinoma; adenocarcinomaUnknown

c.754C>T; p.R252*; 8:17209955-17209955

large_intestinecarcinoma; adenocarcinomaSubstitution - Nonsense

c.724A>T; p.T242S; 8:17208086-17208086

livercarcinomaSubstitution - Missense

c.255C>T; p.F85F; 8:17195506-17195506

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.602G>A; p.G201D; 8:17207964-17207964

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.861A>G; p.L287L; 8:17210391-17210391

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.1028C>T; p.T343M; 8:17215314-17215314

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.493G>A; p.G165R; 8:17205671-17205671

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1023T>C; p.S341S; 8:17215309-17215309

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.911A>G; p.Q304R; 8:17210441-17210441

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.513C>A; p.F171L; 8:17205691-17205691

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.513C>A; p.F171L; 8:17205691-17205691

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.513C>A; p.F171L; 8:17205691-17205691

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.591T>G; p.F197L; 8:17205769-17205769

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.463C>T; p.H155Y; 8:17198400-17198400

skinmalignant_melanomaSubstitution - Missense

c.463C>T; p.H155Y; 8:17198400-17198400

skinmalignant_melanomaSubstitution - Missense

c.766G>T; p.D256Y; 8:17209967-17209967

pancreascarcinomaSubstitution - Missense

c.766G>T; p.D256Y; 8:17209967-17209967

pancreascarcinoma; ductal_carcinomaSubstitution - Missense

c.536C>T; p.S179F; 8:17205714-17205714

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.371G>A; p.G124E; 8:17195622-17195622

skinmalignant_melanomaSubstitution - Missense