General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 1634 |
Name | DCN |
Synonymous | decorin;DCN;decorin |
Definition | PG-S2|bone proteoglycan II|decorin proteoglycan|dermatan sulphate proteoglycans II|proteoglycan core protein|small leucine-rich protein 1B |
Position | 12q21.33 |
Gene Type | protein-coding |
Mutation summary: | Mutations in domains Mutational pattern in 17 major cancer types LoF vs missense mutations All the copy number variations from COSMIC database V72 All the mutations from COSMIC database V72 |
Mutation summary in protein domains | Top |
The non-synonymous (top) and synonymous (bottom) mutational percentage for various cancers | Top |
Loss of Function mutations compare to missense mutations | Top |
The ratio of the loss-of-function mutations over missense mutations is 0.14. |
The copy number variations for various cancers | Top |
The copy number variations in 17 major cancer types: 1; Breast, 2; Central nervous system, 3; Cervix, 4; Endometrium, 5; Haematopoietic and lymphoid_tissue, 6; Kidney, 7; Large intestine, 8; Liver, 9; Lung, 10; Not specific, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary tract |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) |
Site |
Histology |
Mutation Type |
---|---|---|---|
c.661C>T; p.P221S; 12:91153181-91153181 |
skin | malignant_melanoma | Substitution - Missense |
c.661C>T; p.P221S; 12:91153181-91153181 |
skin | malignant_melanoma | Substitution - Missense |
c.2T>C; p.M1T; 12:91178551-91178551 |
skin; arm | malignant_melanoma | Substitution - Missense |
c.296G>A; p.G99E; 12:91164633-91164633 |
skin | malignant_melanoma | Substitution - Missense |
c.1066G>A; p.G356R; 12:91146072-91146072 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1066G>A; p.G356R; 12:91146072-91146072 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.616C>T; p.R206C; 12:91157111-91157111 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.46G>A; p.A16T; 12:91178507-91178507 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.593G>A; p.G198E; 12:91157134-91157134 |
skin | malignant_melanoma | Substitution - Missense |
c.699C>T; p.I233I; 12:91153143-91153143 |
skin | malignant_melanoma | Substitution - coding silent |
c.673G>A; p.E225K; 12:91153169-91153169 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.447C>T; p.P149P; 12:91158387-91158387 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.442_443insA; p.M148fs*12; 12:91158391-91158392 |
large_intestine | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.486C>T; p.I162I; 12:91158348-91158348 |
skin | malignant_melanoma | Substitution - coding silent |
c.532G>A; p.V178I; 12:91158302-91158302 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.623C>T; p.A208V; 12:91157104-91157104 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.765C>A; p.N255K; 12:91151774-91151774 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Missense |
c.653-2A>G; p.?; 12:91153191-91153191 |
liver | carcinoma; hepatocellular_carcinoma | Unknown |
c.49G>A; p.G17R; 12:91178504-91178504 |
skin | malignant_melanoma | Substitution - Missense |
c.420G>T; p.Q140H; 12:91158414-91158414 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.283G>A; p.E95K; 12:91164646-91164646 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.283G>A; p.E95K; 12:91164646-91164646 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.283G>A; p.E95K; 12:91164646-91164646 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.283G>A; p.E95K; 12:91164646-91164646 |
skin | malignant_melanoma | Substitution - Missense |
c.283G>A; p.E95K; 12:91164646-91164646 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.283G>A; p.E95K; 12:91164646-91164646 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.195C>T; p.V65V; 12:91178358-91178358 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.693C>T; p.N231N; 12:91153149-91153149 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.138C>T; p.F46F; 12:91178415-91178415 |
skin | malignant_melanoma | Substitution - coding silent |
c.923G>C; p.G308A; 12:91146215-91146215 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.449A>C; p.K150T; 12:91158385-91158385 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.497G>A; p.R166Q; 12:91158337-91158337 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.29T>C; p.L10P; 12:91178524-91178524 |
skin | malignant_melanoma | Substitution - Missense |
c.127G>T; p.D43Y; 12:91178426-91178426 |
soft_tissue; striated_muscle | rhabdomyosarcoma; embryonal | Substitution - Missense |
c.205G>A; p.D69N; 12:91178348-91178348 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.860G>A; p.G287E; 12:91151679-91151679 |
skin | malignant_melanoma | Substitution - Missense |
c.541C>A; p.L181M; 12:91157186-91157186 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.397C>T; p.R133*; 12:91158437-91158437 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Nonsense |
c.397C>T; p.R133*; 12:91158437-91158437 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Nonsense |
c.1048C>T; p.R350C; 12:91146090-91146090 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.630C>A; p.T210T; 12:91157097-91157097 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.641G>A; p.S214N; 12:91157086-91157086 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.974C>T; p.S325L; 12:91146164-91146164 |
skin | malignant_melanoma | Substitution - Missense |
c.244G>C; p.D82H; 12:91164685-91164685 |
lung | carcinoma; small_cell_carcinoma | Substitution - Missense |
c.612C>T; p.Y204Y; 12:91157115-91157115 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1011G>A; p.W337*; 12:91146127-91146127 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1003C>T; p.Q335*; 12:91146135-91146135 |
skin | malignant_melanoma | Substitution - Nonsense |
c.671C>T; p.T224M; 12:91153171-91153171 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.671C>T; p.T224M; 12:91153171-91153171 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.671C>T; p.T224M; 12:91153171-91153171 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.514G>A; p.G172R; 12:91158320-91158320 |
skin | malignant_melanoma | Substitution - Missense |
c.324+1G>T; p.?; 12:91164604-91164604 |
lung | carcinoma; adenocarcinoma | Unknown |
c.427G>A; p.E143K; 12:91158407-91158407 |
skin | malignant_melanoma | Substitution - Missense |
c.901A>G; p.N301D; 12:91146237-91146237 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1032C>G; p.F344L; 12:91146106-91146106 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1032C>G; p.F344L; 12:91146106-91146106 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.1029C>T; p.T343T; 12:91146109-91146109 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1007A>T; p.Y336F; 12:91146131-91146131 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.399A>G; p.R133R; 12:91158435-91158435 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.399A>G; p.R133R; 12:91158435-91158435 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.399A>G; p.R133R; 12:91158435-91158435 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.882C>T; p.I294I; 12:91151657-91151657 |
skin | malignant_melanoma | Substitution - coding silent |
c.187C>T; p.R63*; 12:91178366-91178366 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.426G>T; p.K142N; 12:91158408-91158408 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.597G>T; p.M199I; 12:91157130-91157130 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.3G>A; p.M1I; 12:91178550-91178550 |
skin | malignant_melanoma | Substitution - Missense |
c.878A>G; p.Y293C; 12:91151661-91151661 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.606C>A; p.L202L; 12:91157121-91157121 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.912C>T; p.I304I; 12:91146226-91146226 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.131G>A; p.R44H; 12:91178422-91178422 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.706G>T; p.V236F; 12:91153136-91153136 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.706G>T; p.V236F; 12:91153136-91153136 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.912C>A; p.I304I; 12:91146226-91146226 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.640A>T; p.S214C; 12:91157087-91157087 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.650A>G; p.Q217R; 12:91157077-91157077 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.650A>G; p.Q217R; 12:91157077-91157077 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1032C>T; p.F344F; 12:91146106-91146106 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.466C>T; p.R156C; 12:91158368-91158368 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1048C>A; p.R350S; 12:91146090-91146090 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.322C>T; p.H108Y; 12:91164607-91164607 |
skin | malignant_melanoma | Substitution - Missense |
c.24_26delTCT; p.L10delL; 12:91178527-91178529 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - In frame |
c.265C>T; p.Q89*; 12:91164664-91164664 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.833A>G; p.N278S; 12:91151706-91151706 |
skin | malignant_melanoma | Substitution - Missense |
c.76G>T; p.D26Y; 12:91178477-91178477 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.288C>A; p.I96I; 12:91164641-91164641 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.1045G>A; p.V349M; 12:91146093-91146093 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.860G>T; p.G287V; 12:91151679-91151679 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.52C>T; p.P18S; 12:91178501-91178501 |
skin | malignant_melanoma | Substitution - Missense |
c.1077_1080delGTAA; p.K359fs?; 12:91146058-91146061 |
endometrium | carcinoma; endometrioid_carcinoma | Deletion - Frameshift |
c.665C>T; p.S222F; 12:91153177-91153177 |
skin | malignant_melanoma | Substitution - Missense |
c.1049G>A; p.R350H; 12:91146089-91146089 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.530T>C; p.I177T; 12:91158304-91158304 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.530T>C; p.I177T; 12:91158304-91158304 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.731T>C; p.L244P; 12:91153111-91153111 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.569G>A; p.G190E; 12:91157158-91157158 |
breast | carcinoma | Substitution - Missense |
c.135C>G; p.D45E; 12:91178418-91178418 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.425A>C; p.K142T; 12:91158409-91158409 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.176A>G; p.Q59R; 12:91178377-91178377 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.502G>A; p.V168I; 12:91158332-91158332 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.523C>T; p.Q175*; 12:91158311-91158311 |
skin | malignant_melanoma | Substitution - Nonsense |
c.121C>T; p.P41S; 12:91178432-91178432 |
skin | malignant_melanoma | Substitution - Missense |
c.662C>A; p.P221H; 12:91153180-91153180 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.325G>A; p.A109T; 12:91158509-91158509 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myeloid_leukaemia | Substitution - Missense |
c.325G>A; p.A109T; 12:91158509-91158509 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; chronic_myeloid_leukaemia | Substitution - Missense |
c.51A>C; p.G17G; 12:91178502-91178502 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.852A>G; p.V284V; 12:91151687-91151687 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.912C>G; p.I304M; 12:91146226-91146226 |
breast | carcinoma | Substitution - Missense |
c.534C>T; p.V178V; 12:91158300-91158300 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.659C>A; p.P220H; 12:91153183-91153183 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.430T>A; p.L144M; 12:91158404-91158404 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.149T>A; p.L50Q; 12:91178404-91178404 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.300C>A; p.D100E; 12:91164629-91164629 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.283G>T; p.E95*; 12:91164646-91164646 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Nonsense |