| General information | Literature | Expression | lncRNA |Regulation | Mutation | Homolog | Interaction |
Basic Information | |||
|---|---|---|---|
Gene ID | 4488 | ||
Name | MSX2 | ||
The somatic mutations from COSMIC database | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.39C>T; p.P13P; 5:174724698-174724698 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.479A>C; p.K160T; 5:174729258-174729258 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; plasma_cell_myeloma | Substitution - Missense |
c.479A>C; p.K160T; 5:174729258-174729258 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.591G>A; p.A197A; 5:174729370-174729370 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.393T>C; p.P131P; 5:174729172-174729172 |
liver | carcinoma | Substitution - coding silent |
c.353A>T; p.E118V; 5:174725012-174725012 |
ovary | other; neoplasm | Substitution - Missense |
c.393T>C; p.P131P; 5:174729172-174729172 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.353A>T; p.E118V; 5:174725012-174725012 |
ovary | other; neoplasm | Substitution - Missense |
c.567G>T; p.W189C; 5:174729346-174729346 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.770C>T; p.T257M; 5:174729549-174729549 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.770C>T; p.T257M; 5:174729549-174729549 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.591G>T; p.A197A; 5:174729370-174729370 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.276C>A; p.P92P; 5:174724935-174724935 |
liver | carcinoma | Substitution - coding silent |
c.276C>A; p.P92P; 5:174724935-174724935 |
liver | carcinoma | Substitution - coding silent |
c.595A>T; p.R199*; 5:174729374-174729374 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Nonsense |
c.771G>A; p.T257T; 5:174729550-174729550 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.148G>T; p.E50*; 5:174724807-174724807 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.338C>T; p.A113V; 5:174724997-174724997 |
skin | malignant_melanoma | Substitution - Missense |
c.496T>C; p.Y166H; 5:174729275-174729275 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.466G>A; p.A156T; 5:174729245-174729245 |
skin; sole | malignant_melanoma; acral_lentiginous | Substitution - Missense |
c.731G>T; p.R244I; 5:174729510-174729510 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.465C>T; p.L155L; 5:174729244-174729244 |
skin | malignant_melanoma | Substitution - coding silent |
c.635C>T; p.A212V; 5:174729414-174729414 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.544A>G; p.T182A; 5:174729323-174729323 |
prostate | carcinoma | Substitution - Missense |
c.387G>A; p.M129I; 5:174729166-174729166 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.368C>T; p.S123L; 5:174725027-174725027 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.773C>T; p.P258L; 5:174729552-174729552 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.791A>G; p.Y264C; 5:174729570-174729570 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.558C>A; p.V186V; 5:174729337-174729337 |
pancreas | carcinoma | Substitution - coding silent |
c.410G>T; p.R137M; 5:174729189-174729189 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.659T>C; p.F220S; 5:174729438-174729438 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.483C>T; p.F161F; 5:174729262-174729262 |
skin | malignant_melanoma | Substitution - coding silent |
c.90C>T; p.G30G; 5:174724749-174724749 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.723G>A; p.P241P; 5:174729502-174729502 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.673C>A; p.P225T; 5:174729452-174729452 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.496T>A; p.Y166N; 5:174729275-174729275 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.437G>A; p.R146H; 5:174729216-174729216 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.437G>A; p.R146H; 5:174729216-174729216 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.695C>T; p.A232V; 5:174729474-174729474 |
breast | carcinoma | Substitution - Missense |
c.434C>T; p.P145L; 5:174729213-174729213 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.503C>T; p.S168F; 5:174729282-174729282 |
breast | carcinoma | Substitution - Missense |
c.472G>A; p.E158K; 5:174729251-174729251 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.698C>T; p.A233V; 5:174729477-174729477 |
pancreas | carcinoma | Substitution - Missense |
c.390C>T; p.S130S; 5:174729169-174729169 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.390C>T; p.S130S; 5:174729169-174729169 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.402C>T; p.C134C; 5:174729181-174729181 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.785G>A; p.G262D; 5:174729564-174729564 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.501C>T; p.L167L; 5:174729280-174729280 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.487C>T; p.Q163*; 5:174729266-174729266 |
breast | carcinoma | Substitution - Nonsense |
c.721C>A; p.P241T; 5:174729500-174729500 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |