| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 3872 |
Name | KRT17 |
Synonymous | keratin 17, type I;KRT17;keratin 17, type I |
Definition | 39.1|CK-17|cytokeratin-17|keratin 17 epitope S1|keratin 17 epitope S2|keratin 17 epitope S4|keratin, type I cytoskeletal 17|keratin-17 |
Position | 17q21.2 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.88C>T; p.R30W; 17:41624422-41624422 |
breast | carcinoma | Substitution - Missense |
c.281G>A; p.R94H; 17:41624229-41624229 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.432+1G>A; p.?; 17:41624077-41624077 |
liver | carcinoma | Unknown |
c.1046T>C; p.V349A; 17:41620794-41620794 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.807G>A; p.K269K; 17:41621620-41621620 |
skin | malignant_melanoma | Substitution - coding silent |
c.1249G>A; p.D417N; 17:41619644-41619644 |
skin | malignant_melanoma | Substitution - Missense |
c.1169G>A; p.G390E; 17:41620671-41620671 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.852C>T; p.R284R; 17:41621074-41621074 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.379C>T; p.P127S; 17:41624131-41624131 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1271G>A; p.R424H; 17:41619622-41619622 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1271G>A; p.R424H; 17:41619622-41619622 |
pancreas | carcinoma | Substitution - Missense |
c.1069C>T; p.R357C; 17:41620771-41620771 |
skin | malignant_melanoma | Substitution - Missense |
c.1069C>T; p.R357C; 17:41620771-41620771 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.244G>A; p.G82R; 17:41624266-41624266 |
skin | malignant_melanoma | Substitution - Missense |
c.769C>T; p.R257C; 17:41621658-41621658 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.769C>T; p.R257C; 17:41621658-41621658 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.770G>A; p.R257H; 17:41621657-41621657 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.209G>A; p.G70D; 17:41624301-41624301 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.968C>T; p.S323F; 17:41620872-41620872 |
skin | malignant_melanoma | Substitution - Missense |
c.1154G>A; p.R385H; 17:41620686-41620686 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.814G>A; p.E272K; 17:41621613-41621613 |
breast | carcinoma | Substitution - Missense |
c.89G>A; p.R30Q; 17:41624421-41624421 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.688C>T; p.R230*; 17:41621739-41621739 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Nonsense |
c.996G>T; p.E332D; 17:41620844-41620844 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.770G>C; p.R257P; 17:41621657-41621657 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1127G>A; p.R376Q; 17:41620713-41620713 |
liver | carcinoma | Substitution - Missense |
c.65delG; p.G22fs*93; 17:41624445-41624445 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.65delG; p.G22fs*93; 17:41624445-41624445 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.65delG; p.G22fs*93; 17:41624445-41624445 |
stomach | carcinoma; intestinal_adenocarcinoma | Deletion - Frameshift |
c.986C>T; p.A329V; 17:41620854-41620854 |
meninges | meningioma | Substitution - Missense |
c.392A>C; p.Y131S; 17:41624118-41624118 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.763G>A; p.E255K; 17:41621664-41621664 |
skin | malignant_melanoma | Substitution - Missense |
c.1057_1058delCT; p.L353fs*>80; 17:41620782-41620783 |
breast | carcinoma | Deletion - Frameshift |
c.1111C>A; p.L371M; 17:41620729-41620729 |
liver | carcinoma | Substitution - Missense |
c.910C>T; p.R304W; 17:41621016-41621016 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.910C>T; p.R304W; 17:41621016-41621016 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_T_cell_leukaemia | Substitution - Missense |
c.986C>G; p.A329G; 17:41620854-41620854 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.961-3C>T; p.?; 17:41620882-41620882 |
liver | carcinoma | Unknown |
c.1124C>T; p.T375M; 17:41620716-41620716 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.903G>A; p.S301S; 17:41621023-41621023 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.718G>A; p.E240K; 17:41621709-41621709 |
skin | malignant_melanoma | Substitution - Missense |
c.935T>A; p.I312K; 17:41620991-41620991 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.698T>G; p.V233G; 17:41621729-41621729 |
breast | carcinoma | Substitution - Missense |
c.681C>T; p.N227N; 17:41621746-41621746 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.295C>T; p.L99L; 17:41624215-41624215 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.803G>A; p.R268H; 17:41621624-41621624 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; Burkitt_lymphoma | Substitution - Missense |
c.572G>A; p.R191H; 17:41622455-41622455 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.254A>G; p.K85R; 17:41624256-41624256 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.751C>T; p.R251C; 17:41621676-41621676 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.508C>T; p.R170C; 17:41622957-41622957 |
breast | carcinoma | Substitution - Missense |
c.1156C>T; p.R386C; 17:41620684-41620684 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1294C>T; p.R432C; 17:41619599-41619599 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1294C>T; p.R432C; 17:41619599-41619599 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.682G>A; p.A228T; 17:41621745-41621745 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.113G>A; p.G38D; 17:41624397-41624397 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.364A>G; p.R122G; 17:41624146-41624146 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.280C>T; p.R94C; 17:41624230-41624230 |
ovary | other; neoplasm | Substitution - Missense |
c.280C>T; p.R94C; 17:41624230-41624230 |
breast | carcinoma | Substitution - Missense |
c.919A>G; p.M307V; 17:41621007-41621007 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.370_371insG; p.A124fs*7; 17:41624139-41624140 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.349C>T; p.R117C; 17:41624161-41624161 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.319G>A; p.E107K; 17:41624191-41624191 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.711C>G; p.I237M; 17:41621716-41621716 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.655A>G; p.K219E; 17:41622372-41622372 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.654G>T; p.L218L; 17:41622373-41622373 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1058T>C; p.L353P; 17:41620782-41620782 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.243T>C; p.A81A; 17:41624267-41624267 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.1054C>A; p.Q352K; 17:41620786-41620786 |
breast | carcinoma | Substitution - Missense |
c.802C>A; p.R268S; 17:41621625-41621625 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.1204+1G>A; p.?; 17:41620535-41620535 |
large_intestine; colon | carcinoma; adenocarcinoma | Unknown |
c.1204+1G>A; p.?; 17:41620535-41620535 |
stomach | carcinoma; adenocarcinoma | Unknown |
c.918C>T; p.T306T; 17:41621008-41621008 |
skin | malignant_melanoma | Substitution - coding silent |
c.657G>A; p.K219K; 17:41622370-41622370 |
skin | malignant_melanoma | Substitution - coding silent |
c.1044C>G; p.S348R; 17:41620796-41620796 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.451G>A; p.D151N; 17:41623014-41623014 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.812C>T; p.A271V; 17:41621615-41621615 |
breast | carcinoma | Substitution - Missense |
c.563A>G; p.N188S; 17:41622464-41622464 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.961-6C>A; p.?; 17:41620885-41620885 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Unknown |
c.139G>A; p.G47S; 17:41624371-41624371 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - Missense |
c.917C>G; p.T306S; 17:41621009-41621009 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1026C>T; p.I342I; 17:41620814-41620814 |
skin | malignant_melanoma | Substitution - coding silent |
c.198T>C; p.G66G; 17:41624312-41624312 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.764A>G; p.E255G; 17:41621663-41621663 |
liver | carcinoma | Substitution - Missense |
c.1047G>A; p.V349V; 17:41620793-41620793 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.128G>A; p.G43E; 17:41624382-41624382 |
skin | malignant_melanoma | Substitution - Missense |
c.128G>A; p.G43E; 17:41624382-41624382 |
skin | malignant_melanoma | Substitution - Missense |
c.128G>A; p.G43E; 17:41624382-41624382 |
skin | malignant_melanoma | Substitution - Missense |
c.1009G>A; p.V337M; 17:41620831-41620831 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.50C>T; p.S17F; 17:41624460-41624460 |
skin | malignant_melanoma | Substitution - Missense |
c.307C>T; p.R103C; 17:41624203-41624203 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.576G>A; p.R192R; 17:41622451-41622451 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.509G>A; p.R170H; 17:41622956-41622956 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.506T>C; p.F169S; 17:41622959-41622959 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1164G>A; p.L388L; 17:41620676-41620676 |
skin | malignant_melanoma | Substitution - coding silent |
c.602G>T; p.R201I; 17:41622425-41622425 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.71C>T; p.S24L; 17:41624439-41624439 |
skin | malignant_melanoma | Substitution - Missense |
c.1030G>T; p.G344W; 17:41620810-41620810 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.900C>T; p.I300I; 17:41621026-41621026 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1207G>A; p.V403M; 17:41619686-41619686 |
skin | malignant_melanoma | Substitution - Missense |
c.752G>A; p.R251H; 17:41621675-41621675 |
prostate | adenoma | Substitution - Missense |
c.752G>A; p.R251H; 17:41621675-41621675 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.288C>A; p.A96A; 17:41624222-41624222 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.605C>A; p.A202D; 17:41622422-41622422 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.517T>G; p.F173V; 17:41622510-41622510 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.248G>T; p.G83V; 17:41624262-41624262 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1166A>T; p.E389V; 17:41620674-41620674 |
skin | malignant_melanoma | Substitution - Missense |
c.496G>T; p.A166S; 17:41622969-41622969 |
breast | carcinoma | Substitution - Missense |
c.757C>T; p.L253F; 17:41621670-41621670 |
skin | malignant_melanoma | Substitution - Missense |
c.1182-8delT; p.?; 17:41620566-41620566 |
liver | carcinoma | Unknown |
c.1157G>A; p.R386H; 17:41620683-41620683 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |