| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 57120 |
Name | GOPC |
Synonymous | golgi-associated PDZ and coiled-coil motif containing;GOPC;golgi-associated PDZ and coiled-coil motif containing |
Definition | CFTR-associated ligand|Golgi associated PDZ and coiled-coil motif containing protein|Golgi-associated PDZ and coiled-coil motif-containing protein|PDZ protein interacting specifically with TC10|PDZ/coiled-coil domain binding partner for the rho-family GTP |
Position | 6q21 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.684G>A; p.M228I; 6:117573599-117573599 |
breast | carcinoma | Substitution - Missense |
c.807A>C; p.P269P; 6:117573476-117573476 |
breast | carcinoma | Substitution - coding silent |
c.294G>C; p.L98F; 6:117579056-117579056 |
breast | carcinoma | Substitution - Missense |
c.853C>A; p.P285T; 6:117570919-117570919 |
breast | carcinoma | Substitution - Missense |
c.1383_1385delTTA; p.Y462delY; 6:117563258-117563260 |
breast | carcinoma | Deletion - In frame |
c.817G>T; p.D273Y; 6:117570955-117570955 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.537G>T; p.V179V; 6:117575290-117575290 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.257C>T; p.S86F; 6:117602032-117602032 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1259G>T; p.G420V; 6:117563384-117563384 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.490G>A; p.A164T; 6:117575337-117575337 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.773G>T; p.G258V; 6:117573510-117573510 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; diffuse_large_B_cell_lymphoma | Substitution - Missense |
c.14G>A; p.G5D; 6:117602275-117602275 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.351A>T; p.K117N; 6:117578999-117578999 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.816+2T>C; p.?; 6:117573465-117573465 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.50delG; p.G17fs*54; 6:117602239-117602239 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.132T>C; p.A44A; 6:117602157-117602157 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.132T>C; p.A44A; 6:117602157-117602157 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.981C>T; p.C327C; 6:117569668-117569668 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1214G>A; p.G405D; 6:117566898-117566898 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1074G>T; p.Q358H; 6:117569575-117569575 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1021G>A; p.G341R; 6:117569628-117569628 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.761G>A; p.R254Q; 6:117573522-117573522 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1044G>T; p.K348N; 6:117569605-117569605 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.731T>G; p.I244R; 6:117573552-117573552 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.731T>G; p.I244R; 6:117573552-117573552 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.608C>T; p.A203V; 6:117575219-117575219 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1326G>A; p.P442P; 6:117563317-117563317 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.157G>T; p.G53*; 6:117602132-117602132 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1262T>G; p.F421C; 6:117563381-117563381 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.568C>T; p.R190C; 6:117575259-117575259 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.944T>C; p.I315T; 6:117569705-117569705 |
liver | carcinoma | Substitution - Missense |
c.819T>G; p.D273E; 6:117570953-117570953 |
liver | carcinoma | Substitution - Missense |
c.912+5G>T; p.?; 6:117570855-117570855 |
liver | carcinoma | Unknown |
c.912+5G>T; p.?; 6:117570855-117570855 |
liver | carcinoma | Unknown |
c.462T>A; p.S154S; 6:117577460-117577460 |
liver | carcinoma | Substitution - coding silent |
c.682A>G; p.M228V; 6:117573601-117573601 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.1078-1G>C; p.?; 6:117567035-117567035 |
lung | carcinoma; adenocarcinoma | Unknown |
c.645A>C; p.A215A; 6:117575182-117575182 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.487G>C; p.E163Q; 6:117575340-117575340 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1028A>C; p.N343T; 6:117569621-117569621 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.289C>G; p.Q97E; 6:117579061-117579061 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.767G>T; p.C256F; 6:117573516-117573516 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Missense |
c.973G>A; p.D325N; 6:117569676-117569676 |
oesophagus | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.434C>T; p.T145I; 6:117578916-117578916 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.351A>C; p.K117N; 6:117578999-117578999 |
ovary | carcinoma; clear_cell_carcinoma | Substitution - Missense |
c.1013C>T; p.A338V; 6:117569636-117569636 |
pancreas | carcinoma | Substitution - Missense |
c.1245C>T; p.I415I; 6:117566867-117566867 |
skin | malignant_melanoma | Substitution - coding silent |
c.422C>T; p.A141V; 6:117578928-117578928 |
skin | malignant_melanoma | Substitution - Missense |
c.601T>A; p.Y201N; 6:117575226-117575226 |
skin | malignant_melanoma | Substitution - Missense |
c.829C>A; p.L277I; 6:117570943-117570943 |
skin | malignant_melanoma | Substitution - Missense |
c.73C>T; p.P25S; 6:117602216-117602216 |
skin | malignant_melanoma | Substitution - Missense |
c.588C>T; p.L196L; 6:117575239-117575239 |
skin | malignant_melanoma | Substitution - coding silent |
c.458C>T; p.P153L; 6:117577464-117577464 |
skin | malignant_melanoma | Substitution - Missense |
c.761G>A; p.R254Q; 6:117573522-117573522 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.811G>T; p.G271C; 6:117573472-117573472 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1359G>A; p.L453L; 6:117563284-117563284 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.51C>T; p.G17G; 6:117602238-117602238 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1337G>A; p.G446D; 6:117563306-117563306 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1020C>T; p.N340N; 6:117569629-117569629 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.677G>A; p.R226Q; 6:117573606-117573606 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.301C>T; p.L101L; 6:117579049-117579049 |
thyroid | carcinoma | Substitution - coding silent |