| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 3985 |
Name | LIMK2 |
Synonymous | LIM domain kinase 2;LIMK2;LIM domain kinase 2 |
Definition | - |
Position | 22q12.2 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.1052A>C; p.K351T; 22:31266994-31266994 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1900C>A; p.R634R; 22:31278424-31278424 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.529G>T; p.A177S; 22:31260055-31260055 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.986G>C; p.C329S; 22:31266077-31266077 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.213C>A; p.F71L; 22:31258387-31258387 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1254C>T; p.R418R; 22:31267901-31267901 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1559G>T; p.G520V; 22:31273452-31273452 |
ovary | carcinoma; adenocarcinoma | Substitution - Missense |
c.1586T>C; p.I529T; 22:31273479-31273479 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.468G>A; p.P156P; 22:31259994-31259994 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1824delG; p.E610fs*17; 22:31278348-31278348 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.758T>C; p.L253P; 22:31262695-31262695 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1260G>T; p.M420I; 22:31267907-31267907 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.503C>T; p.S168F; 22:31260029-31260029 |
skin | malignant_melanoma | Substitution - Missense |
c.839G>T; p.R280M; 22:31262776-31262776 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1253G>A; p.R418H; 22:31267900-31267900 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1220A>G; p.Y407C; 22:31267867-31267867 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1090C>T; p.R364*; 22:31267032-31267032 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.1090C>T; p.R364*; 22:31267032-31267032 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.1090C>T; p.R364*; 22:31267032-31267032 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1090C>T; p.R364*; 22:31267032-31267032 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.1380G>A; p.K460K; 22:31271198-31271198 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1041+7G>A; p.?; 22:31266139-31266139 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Unknown |
c.1041+7G>A; p.?; 22:31266139-31266139 |
central_nervous_system; brain | glioma | Unknown |
c.1765G>T; p.E589*; 22:31275301-31275301 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.912G>C; p.L304L; 22:31266003-31266003 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.946C>T; p.R316C; 22:31266037-31266037 |
skin | malignant_melanoma | Substitution - Missense |
c.1451C>A; p.P484H; 22:31272597-31272597 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.954C>T; p.S318S; 22:31266045-31266045 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.946C>T; p.R316C; 22:31266037-31266037 |
skin; scalp | malignant_melanoma | Substitution - Missense |
c.1173C>T; p.F391F; 22:31267820-31267820 |
skin | malignant_melanoma | Substitution - coding silent |
c.946C>T; p.R316C; 22:31266037-31266037 |
skin | malignant_melanoma | Substitution - Missense |
c.409_410delCT; p.S138fs*22; 22:31259935-31259936 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.657G>T; p.E219D; 22:31262239-31262239 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1541C>T; p.A514V; 22:31272687-31272687 |
ovary | other; neoplasm | Substitution - Missense |
c.1541C>T; p.A514V; 22:31272687-31272687 |
ovary | other; neoplasm | Substitution - Missense |
c.1372C>G; p.L458V; 22:31271190-31271190 |
pancreas | carcinoma | Substitution - Missense |
c.980G>A; p.R327Q; 22:31266071-31266071 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1439G>T; p.R480M; 22:31272585-31272585 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.422C>T; p.S141F; 22:31259948-31259948 |
skin | malignant_melanoma | Substitution - Missense |
c.975C>G; p.I325M; 22:31266066-31266066 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1602C>T; p.I534I; 22:31273495-31273495 |
skin | malignant_melanoma | Substitution - coding silent |
c.979C>T; p.R327W; 22:31266070-31266070 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.571A>G; p.S191G; 22:31262153-31262153 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.817G>A; p.E273K; 22:31262754-31262754 |
skin | malignant_melanoma | Substitution - Missense |
c.1902G>A; p.R634R; 22:31278426-31278426 |
skin | malignant_melanoma | Substitution - coding silent |
c.546G>T; p.V182V; 22:31260072-31260072 |
skin | malignant_melanoma | Substitution - coding silent |
c.1348C>T; p.R450W; 22:31271166-31271166 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.153C>A; p.Y51*; 22:31258327-31258327 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.153C>A; p.Y51*; 22:31258327-31258327 |
large_intestine; colon | carcinoma | Substitution - Nonsense |
c.153C>A; p.Y51*; 22:31258327-31258327 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1800C>A; p.S600S; 22:31278324-31278324 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.22G>A; p.D8N; 22:31225725-31225725 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1608C>T; p.L536L; 22:31273501-31273501 |
skin | malignant_melanoma | Substitution - coding silent |
c.996C>T; p.I332I; 22:31266087-31266087 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1239G>A; p.L413L; 22:31267886-31267886 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.607C>G; p.R203G; 22:31262189-31262189 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.15G>A; p.A5A; 22:31212423-31212423 |
skin | malignant_melanoma | Substitution - coding silent |
c.307G>A; p.V103M; 22:31259175-31259175 |
breast | carcinoma | Substitution - Missense |
c.99G>A; p.W33*; 22:31225802-31225802 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.689C>G; p.T230R; 22:31262626-31262626 |
skin | malignant_melanoma | Substitution - Missense |
c.1785G>A; p.S595S; 22:31278309-31278309 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1421G>A; p.R474Q; 22:31272567-31272567 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1725_1727delCTT; p.F577delF; 22:31275261-31275263 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - In frame |
c.932G>T; p.R311L; 22:31266023-31266023 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.932G>T; p.R311L; 22:31266023-31266023 |
central_nervous_system; brainstem | glioma; astrocytoma_Grade_III | Substitution - Missense |
c.1901G>T; p.R634L; 22:31278425-31278425 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.607C>T; p.R203C; 22:31262189-31262189 |
bone; femur | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.1201C>T; p.L401L; 22:31267848-31267848 |
skin | malignant_melanoma | Substitution - coding silent |
c.1236A>G; p.T412T; 22:31267883-31267883 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.504C>T; p.S168S; 22:31260030-31260030 |
skin | malignant_melanoma | Substitution - coding silent |
c.1232G>C; p.G411A; 22:31267879-31267879 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.819G>T; p.E273D; 22:31262756-31262756 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1645T>G; p.C549G; 22:31275181-31275181 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.372C>T; p.C124C; 22:31259898-31259898 |
bone; rib | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.198G>A; p.G66G; 22:31258372-31258372 |
skin | malignant_melanoma | Substitution - coding silent |
c.730C>T; p.L244L; 22:31262667-31262667 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.398T>C; p.M133T; 22:31259924-31259924 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.1333A>G; p.M445V; 22:31271151-31271151 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1020_1021CT>AG; p.F341V; 22:31266111-31266112 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.551+2T>C; p.?; 22:31260079-31260079 |
pancreas | carcinoma | Unknown |
c.551+2T>C; p.?; 22:31260079-31260079 |
pancreas | carcinoma | Unknown |
c.551+2T>C; p.?; 22:31260079-31260079 |
pancreas | carcinoma | Unknown |
c.857G>A; p.R286H; 22:31265948-31265948 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1415T>G; p.L472R; 22:31272561-31272561 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1415T>G; p.L472R; 22:31272561-31272561 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.988G>A; p.D330N; 22:31266079-31266079 |
breast | carcinoma | Substitution - Missense |
c.1863G>A; p.E621E; 22:31278387-31278387 |
autonomic_ganglia | neuroblastoma | Substitution - coding silent |
c.1363C>A; p.H455N; 22:31271181-31271181 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.16+1G>T; p.?; 22:31212425-31212425 |
large_intestine; rectum | carcinoma; adenocarcinoma | Unknown |
c.1367A>C; p.N456T; 22:31271185-31271185 |
skin | malignant_melanoma | Substitution - Missense |
c.1606C>G; p.L536V; 22:31273499-31273499 |
skin | malignant_melanoma | Substitution - Missense |
c.901G>C; p.E301Q; 22:31265992-31265992 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1093T>C; p.C365R; 22:31267035-31267035 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.622A>T; p.N208Y; 22:31262204-31262204 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.942C>T; p.S314S; 22:31266033-31266033 |
skin | malignant_melanoma | Substitution - coding silent |
c.646C>T; p.R216*; 22:31262228-31262228 |
skin; trunk | malignant_melanoma | Substitution - Nonsense |
c.453G>A; p.T151T; 22:31259979-31259979 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.262G>A; p.E88K; 22:31259130-31259130 |
skin | malignant_melanoma | Substitution - Missense |
c.1110G>A; p.Q370Q; 22:31267052-31267052 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.1843C>T; p.L615L; 22:31278367-31278367 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1562A>G; p.K521R; 22:31273455-31273455 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.626G>T; p.G209V; 22:31262208-31262208 |
breast | carcinoma | Substitution - Missense |
c.608G>A; p.R203H; 22:31262190-31262190 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.608G>A; p.R203H; 22:31262190-31262190 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.608G>A; p.R203H; 22:31262190-31262190 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.608G>A; p.R203H; 22:31262190-31262190 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1897A>G; p.T633A; 22:31278421-31278421 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.771G>A; p.M257I; 22:31262708-31262708 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1614G>T; p.E538D; 22:31273507-31273507 |
ovary | carcinoma | Substitution - Missense |
c.1839C>T; p.I613I; 22:31278363-31278363 |
skin | malignant_melanoma | Substitution - coding silent |
c.103G>A; p.G35S; 22:31225806-31225806 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.91G>A; p.E31K; 22:31225794-31225794 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.752C>T; p.A251V; 22:31262689-31262689 |
breast | carcinoma | Substitution - Missense |
c.91G>A; p.E31K; 22:31225794-31225794 |
skin | malignant_melanoma | Substitution - Missense |
c.1044G>T; p.V348V; 22:31266986-31266986 |
prostate | carcinoma | Substitution - coding silent |
c.1332_1333delTA; p.M445fs*71; 22:31271150-31271151 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.905C>T; p.P302L; 22:31265996-31265996 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.599C>A; p.P200H; 22:31262181-31262181 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.558C>G; p.N186K; 22:31262140-31262140 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1265C>T; p.P422L; 22:31268148-31268148 |
skin | malignant_melanoma | Substitution - Missense |
c.1265C>T; p.P422L; 22:31268148-31268148 |
kidney | Wilms_tumour | Substitution - Missense |
c.1578G>A; p.T526T; 22:31273471-31273471 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1563G>A; p.K521K; 22:31273456-31273456 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.452C>T; p.T151M; 22:31259978-31259978 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1478G>A; p.R493H; 22:31272624-31272624 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.452C>T; p.T151M; 22:31259978-31259978 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |