| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 200081 |
Name | TXLNA |
Synonymous | taxilin alpha;TXLNA;taxilin alpha |
Definition | alpha-taxilin|interleukin 14 |
Position | 1p35.1 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.614A>C; p.N205T; 1:32187970-32187970 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1563G>A; p.A521A; 1:32195117-32195117 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.539A>C; p.N180T; 1:32184558-32184558 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.966T>C; p.H322H; 1:32192313-32192313 |
thyroid | other; neoplasm | Substitution - coding silent |
c.187G>A; p.A63T; 1:32181259-32181259 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.331G>C; p.E111Q; 1:32181403-32181403 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.332A>T; p.E111V; 1:32181404-32181404 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.331G>C; p.E111Q; 1:32181403-32181403 |
lung | carcinoma; mixed_small_cell_carcinoma-adenocarcinoma | Substitution - Missense |
c.685G>A; p.G229S; 1:32188041-32188041 |
skin | malignant_melanoma | Substitution - Missense |
c.554C>T; p.P185L; 1:32184573-32184573 |
skin | malignant_melanoma | Substitution - Missense |
c.554C>T; p.P185L; 1:32184573-32184573 |
skin | malignant_melanoma | Substitution - Missense |
c.276delG; p.G94fs*35; 1:32181348-32181348 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.276delG; p.G94fs*35; 1:32181348-32181348 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.276delG; p.G94fs*35; 1:32181348-32181348 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.276delG; p.G94fs*35; 1:32181348-32181348 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.712C>T; p.R238C; 1:32188068-32188068 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.447C>T; p.D149D; 1:32181519-32181519 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.391_392GG>AA; p.G131K; 1:32181463-32181464 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1052C>T; p.A351V; 1:32192399-32192399 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1454T>C; p.V485A; 1:32195008-32195008 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1525G>A; p.G509R; 1:32195079-32195079 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.292G>A; p.D98N; 1:32181364-32181364 |
skin; mucosal | malignant_melanoma | Substitution - Missense |
c.254C>T; p.T85I; 1:32181326-32181326 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.896G>A; p.R299H; 1:32190182-32190182 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.182G>C; p.R61T; 1:32181254-32181254 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1613C>T; p.P538L; 1:32195167-32195167 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.448G>A; p.E150K; 1:32181520-32181520 |
oesophagus | carcinoma | Substitution - Missense |
c.1304G>A; p.R435Q; 1:32194117-32194117 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.14A>T; p.D5V; 1:32180359-32180359 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.153T>C; p.A51A; 1:32180498-32180498 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - coding silent |
c.797A>C; p.E266A; 1:32190083-32190083 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.797A>C; p.E266A; 1:32190083-32190083 |
liver | carcinoma | Substitution - Missense |
c.1155A>G; p.Q385Q; 1:32192728-32192728 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1231T>C; p.F411L; 1:32193280-32193280 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1026G>T; p.Q342H; 1:32192373-32192373 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.970G>C; p.D324H; 1:32192317-32192317 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.995T>A; p.L332Q; 1:32192342-32192342 |
breast | carcinoma | Substitution - Missense |
c.916G>C; p.A306P; 1:32190202-32190202 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1480G>T; p.G494C; 1:32195034-32195034 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.597+1G>A; p.?; 1:32184617-32184617 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Unknown |
c.1504G>A; p.E502K; 1:32195058-32195058 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1025A>G; p.Q342R; 1:32192372-32192372 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1307G>T; p.W436L; 1:32194120-32194120 |
skin; extremity | malignant_melanoma | Substitution - Missense |
c.969C>T; p.I323I; 1:32192316-32192316 |
skin | malignant_melanoma | Substitution - coding silent |
c.956G>A; p.R319H; 1:32190242-32190242 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.969C>T; p.I323I; 1:32192316-32192316 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1526G>T; p.G509V; 1:32195080-32195080 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.205C>T; p.R69C; 1:32181277-32181277 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.205C>T; p.R69C; 1:32181277-32181277 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.139_140GG>AA; p.G47N; 1:32180484-32180485 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.978C>G; p.V326V; 1:32192325-32192325 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1589C>T; p.T530I; 1:32195143-32195143 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.26G>A; p.G9E; 1:32180371-32180371 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.389A>G; p.N130S; 1:32181461-32181461 |
thyroid | other; neoplasm | Substitution - Missense |
c.704T>C; p.V235A; 1:32188060-32188060 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.704T>C; p.V235A; 1:32188060-32188060 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.704T>C; p.V235A; 1:32188060-32188060 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.970G>A; p.D324N; 1:32192317-32192317 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1187A>T; p.E396V; 1:32193236-32193236 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.953_954insG; p.R319fs*56; 1:32190239-32190240 |
endometrium | carcinoma; endometrioid_carcinoma | Insertion - Frameshift |
c.400G>A; p.E134K; 1:32181472-32181472 |
breast | carcinoma | Substitution - Missense |
c.1562C>T; p.A521V; 1:32195116-32195116 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.667G>C; p.E223Q; 1:32188023-32188023 |
upper_aerodigestive_tract; pharynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.736C>A; p.R246S; 1:32188092-32188092 |
skin | malignant_melanoma | Substitution - Missense |
c.392G>A; p.G131E; 1:32181464-32181464 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1621C>T; p.P541S; 1:32195175-32195175 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1031C>T; p.A344V; 1:32192378-32192378 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.651G>C; p.Q217H; 1:32188007-32188007 |
breast | carcinoma | Substitution - Missense |
c.784C>T; p.R262W; 1:32190070-32190070 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.737G>T; p.R246L; 1:32188093-32188093 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1432C>T; p.R478C; 1:32194986-32194986 |
pancreas | carcinoma | Substitution - Missense |
c.244A>C; p.I82L; 1:32181316-32181316 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.849C>T; p.D283D; 1:32190135-32190135 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.785G>T; p.R262L; 1:32190071-32190071 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1396C>T; p.R466W; 1:32194950-32194950 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.230G>A; p.R77H; 1:32181302-32181302 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |