| Gene information | Literature | Expression | lncRNA | Mutation | Homolog |
Basic Information | |
|---|---|
Gene ID | 5036 |
Name | PA2G4 |
Synonymous | proliferation-associated 2G4, 38kDa;PA2G4;proliferation-associated 2G4, 38kDa |
Definition | ErbB-3 binding protein 1|ErbB3-binding protein Ebp1|cell cycle protein p38-2G4 homolog|erbB3-binding protein 1|proliferation-associated 2G4, 38kD|proliferation-associated protein 2G4 |
Position | 12q13.2 |
Gene Type | protein-coding |
COSMIC confirmed somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.550G>A; p.G184S; 12:56109293-56109293 |
biliary_tract; bile_duct | carcinoma; adenocarcinoma | Substitution - Missense |
c.963T>C; p.F321F; 12:56111207-56111207 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1180G>T; p.D394Y; 12:56112883-56112883 |
breast | carcinoma | Substitution - Missense |
c.795C>G; p.F265L; 12:56110645-56110645 |
breast | carcinoma | Substitution - Missense |
c.868C>G; p.R290G; 12:56110989-56110989 |
breast | carcinoma | Substitution - Missense |
c.687C>T; p.L229L; 12:56110456-56110456 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.868C>T; p.R290W; 12:56110989-56110989 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.711C>T; p.A237A; 12:56110561-56110561 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.392A>G; p.Q131R; 12:56107255-56107255 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.994C>T; p.R332W; 12:56111238-56111238 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.408A>G; p.T136T; 12:56107535-56107535 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.745C>T; p.R249*; 12:56110595-56110595 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.889G>A; p.A297T; 12:56111010-56111010 |
endometrium | carcinoma; serous_carcinoma | Substitution - Missense |
c.586G>T; p.D196Y; 12:56109892-56109892 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1116G>T; p.K372N; 12:56111526-56111526 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.355G>A; p.A119T; 12:56107218-56107218 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.355G>A; p.A119T; 12:56107218-56107218 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia_therapy_related | Substitution - Missense |
c.593delA; p.T200fs*58; 12:56109899-56109899 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Deletion - Frameshift |
c.1108delA; p.K372fs*16; 12:56111518-56111518 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1108delA; p.K372fs*16; 12:56111518-56111518 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.460C>A; p.L154I; 12:56107587-56107587 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.781A>G; p.T261A; 12:56110631-56110631 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.49G>A; p.V17I; 12:56104786-56104786 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1148G>C; p.S383T; 12:56112851-56112851 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1161_1163delAGA; p.E389delE; 12:56112864-56112866 |
large_intestine | carcinoma; adenocarcinoma | Deletion - In frame |
c.1034C>T; p.S345F; 12:56111278-56111278 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.728G>T; p.R243I; 12:56110578-56110578 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.736A>G; p.I246V; 12:56110586-56110586 |
liver | carcinoma | Substitution - Missense |
c.736A>G; p.I246V; 12:56110586-56110586 |
liver | carcinoma | Substitution - Missense |
c.217+3delA; p.?; 12:56106719-56106719 |
liver | carcinoma | Unknown |
c.726G>T; p.Q242H; 12:56110576-56110576 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.726G>T; p.Q242H; 12:56110576-56110576 |
lung | carcinoma; bronchioloalveolar_adenocarcinoma | Substitution - Missense |
c.214A>T; p.K72*; 12:56106713-56106713 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.73G>A; p.G25S; 12:56104810-56104810 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.272C>A; p.P91H; 12:56107044-56107044 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.331_332GG>TT; p.G111L; 12:56107194-56107195 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.662A>T; p.H221L; 12:56110431-56110431 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Missense |
c.210G>T; p.M70I; 12:56106709-56106709 |
NS | NS | Substitution - Missense |
c.792C>A; p.A264A; 12:56110642-56110642 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.869G>A; p.R290Q; 12:56110990-56110990 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1028A>G; p.Y343C; 12:56111272-56111272 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.217+3delA; p.?; 12:56106719-56106719 |
ovary | carcinoma; serous_carcinoma | Unknown |
c.1108delA; p.K372fs*16; 12:56111518-56111518 |
pancreas | carcinoma; acinar_carcinoma | Deletion - Frameshift |
c.683T>C; p.V228A; 12:56110452-56110452 |
skin | malignant_melanoma | Substitution - Missense |
c.963T>C; p.F321F; 12:56111207-56111207 |
skin | malignant_melanoma | Substitution - coding silent |
c.753C>T; p.P251P; 12:56110603-56110603 |
skin | malignant_melanoma | Substitution - coding silent |
c.607C>G; p.Q203E; 12:56109913-56109913 |
skin | malignant_melanoma | Substitution - Missense |
c.814C>T; p.R272C; 12:56110664-56110664 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.980C>A; p.P327H; 12:56111224-56111224 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.972G>A; p.L324L; 12:56111216-56111216 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.973C>A; p.L325I; 12:56111217-56111217 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.158A>G; p.D53G; 12:56106657-56106657 |
thyroid | carcinoma | Substitution - Missense |
c.248A>G; p.N83S; 12:56107020-56107020 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1101G>C; p.Q367H; 12:56111511-56111511 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.191T>C; p.F64S; 12:56106690-56106690 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.191T>C; p.F64S; 12:56106690-56106690 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |