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

Basic Information

Gene ID

4015

Name

LOX

The somatic mutations from COSMIC database

Mutation (CDS; AA; Chr)

Site

Histology

Mutation Type

c.1247+1G>A; p.?; 5:122070052-122070052

 large_intestine; coloncarcinoma; adenocarcinomaUnknown

c.1247+1G>A; p.?; 5:122070052-122070052

 stomachcarcinoma; adenocarcinomaUnknown

c.464G>A; p.S155N; 5:122077522-122077522

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.555C>A; p.N185K; 5:122077431-122077431

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.955C>T; p.H319Y; 5:122074093-122074093

 thyroidcarcinomaSubstitution - Missense

c.62G>A; p.C21Y; 5:122077924-122077924

 stomachcarcinoma; intestinal_adenocarcinomaSubstitution - Missense

c.53T>C; p.L18P; 5:122077933-122077933

 skinmalignant_melanomaSubstitution - Missense

c.1229C>G; p.S410*; 5:122070071-122070071

 urinary_tract; bladdercarcinomaSubstitution - Nonsense

c.499G>A; p.V167M; 5:122077487-122077487

 prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.680A>G; p.Y227C; 5:122076953-122076953

 kidneycarcinoma; papillary_renal_cell_carcinomaSubstitution - Missense

c.99C>T; p.R33R; 5:122077887-122077887

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.117G>A; p.P39P; 5:122077869-122077869

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.1010G>A; p.R337Q; 5:122074038-122074038

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1246C>A; p.P416T; 5:122070054-122070054

 lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.493G>C; p.G165R; 5:122077493-122077493

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.426G>A; p.A142A; 5:122077560-122077560

 thyroidcarcinomaSubstitution - coding silent

c.364C>T; p.R122C; 5:122077622-122077622

 large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.364C>T; p.R122C; 5:122077622-122077622

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1037G>A; p.G346E; 5:122070588-122070588

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.419C>T; p.S140L; 5:122077567-122077567

 urinary_tract; bladdercarcinomaSubstitution - Missense

c.316A>G; p.T106A; 5:122077670-122077670

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.740G>T; p.S247I; 5:122076893-122076893

 lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.80G>A; p.G27D; 5:122077906-122077906

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.273C>T; p.I91I; 5:122077713-122077713

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.978A>G; p.E326E; 5:122074070-122074070

 skinmalignant_melanomaSubstitution - coding silent

c.436A>G; p.T146A; 5:122077550-122077550

 upper_aerodigestive_tract; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.768T>G; p.D256E; 5:122075514-122075514

 kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.424G>A; p.A142T; 5:122077562-122077562

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.244G>A; p.A82T; 5:122077742-122077742

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.916delC; p.L306fs*42; 5:122074132-122074132

 lungcarcinoma; adenocarcinomaDeletion - Frameshift

c.842G>A; p.R281Q; 5:122075440-122075440

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.842G>A; p.R281Q; 5:122075440-122075440

 large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.473G>A; p.R158Q; 5:122077513-122077513

 breastcarcinomaSubstitution - Missense

c.550T>C; p.Y184H; 5:122077436-122077436

 livercarcinomaSubstitution - Missense

c.1235G>C; p.C412S; 5:122070065-122070065

 biliary_tract; bile_ductcarcinoma; adenocarcinomaSubstitution - Missense

c.550T>C; p.Y184H; 5:122077436-122077436

 livercarcinomaSubstitution - Missense

c.876T>A; p.H292Q; 5:122075406-122075406

 lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.1246_1247CC>TT; p.P416L; 5:122070053-122070054

 skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1233C>A; p.G411G; 5:122070067-122070067

 lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.320C>T; p.A107V; 5:122077666-122077666

 large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.652G>A; p.D218N; 5:122076981-122076981

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1201C>T; p.R401C; 5:122070099-122070099

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.968T>G; p.F323C; 5:122074080-122074080

 skinmalignant_melanomaSubstitution - Missense

c.1036-1G>A; p.?; 5:122070590-122070590

 kidneycarcinoma; clear_cell_renal_cell_carcinomaUnknown

c.690G>T; p.K230N; 5:122076943-122076943

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1023T>C; p.T341T; 5:122074025-122074025

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.49G>A; p.A17T; 5:122077937-122077937

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1248-1G>C; p.?; 5:122066750-122066750

 lungcarcinoma; small_cell_carcinomaUnknown

c.809A>G; p.K270R; 5:122075473-122075473

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1003C>A; p.H335N; 5:122074045-122074045

 lungcarcinoma; adenocarcinomaSubstitution - Missense

c.450A>C; p.E150D; 5:122077536-122077536

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.734T>A; p.L245Q; 5:122076899-122076899

 lungcarcinoma; non_small_cell_carcinomaSubstitution - Missense

c.841C>T; p.R281*; 5:122075441-122075441

 breastcarcinomaSubstitution - Nonsense

c.925G>A; p.A309T; 5:122074123-122074123

 stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.765A>C; p.R255S; 5:122075517-122075517

 large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1045C>T; p.P349S; 5:122070580-122070580

 skinmalignant_melanomaSubstitution - Missense

c.1045C>T; p.P349S; 5:122070580-122070580

 skinmalignant_melanomaSubstitution - Missense

c.1220C>T; p.A407V; 5:122070080-122070080

 endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.1020T>C; p.C340C; 5:122074028-122074028

 stomachcarcinoma; adenocarcinomaSubstitution - coding silent

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