General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
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Gene ID | 22943 |
Name | DKK1 |
Synonymous | dickkopf WNT signaling pathway inhibitor 1;DKK1;dickkopf WNT signaling pathway inhibitor 1 |
Definition | dickkopf 1 homolog|dickkopf related protein-1|dickkopf-1 like|dickkopf-like protein 1|dickkopf-related protein 1|hDkk-1 |
Position | 10q11.2 |
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 0.10. |
The copy number variations for various cancers | Top |
There is no record for DKK1 |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) |
Site |
Histology |
Mutation Type |
---|---|---|---|
c.182G>T; p.S61I; 10:52314616-52314616 |
liver | carcinoma | Substitution - Missense |
c.167C>A; p.P56Q; 10:52314601-52314601 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.183C>T; p.S61S; 10:52314617-52314617 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.390G>A; p.G130G; 10:52315069-52315069 |
skin | malignant_melanoma | Substitution - coding silent |
c.140C>A; p.P47Q; 10:52314574-52314574 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.187G>T; p.A63S; 10:52314621-52314621 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.358C>T; p.R120C; 10:52315037-52315037 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.113A>C; p.N38T; 10:52314547-52314547 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.579A>G; p.S193S; 10:52316585-52316585 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.99G>A; p.L33L; 10:52314533-52314533 |
breast | carcinoma | Substitution - coding silent |
c.551A>G; p.Q184R; 10:52316557-52316557 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.352C>T; p.R118*; 10:52315031-52315031 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.352C>T; p.R118*; 10:52315031-52315031 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.245C>A; p.P82Q; 10:52314924-52314924 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.633A>G; p.K211K; 10:52316639-52316639 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.433C>T; p.H145Y; 10:52316321-52316321 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.176C>A; p.A59E; 10:52314610-52314610 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.64G>A; p.G22S; 10:52314498-52314498 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.332G>T; p.C111F; 10:52315011-52315011 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.539A>C; p.H180P; 10:52316427-52316427 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.770C>T; p.S257F; 10:52316776-52316776 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.661A>G; p.T221A; 10:52316667-52316667 |
skin | malignant_melanoma | Substitution - Missense |
c.463A>G; p.T155A; 10:52316351-52316351 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.120C>A; p.N40K; 10:52314554-52314554 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.566G>C; p.C189S; 10:52316572-52316572 |
large_intestine; rectum | NS | Substitution - Missense |
c.320G>A; p.G107D; 10:52314999-52314999 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.91G>A; p.A31T; 10:52314525-52314525 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.748G>A; p.D250N; 10:52316754-52316754 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.748G>A; p.D250N; 10:52316754-52316754 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.674G>A; p.R225K; 10:52316680-52316680 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - Missense |
c.501G>A; p.G167G; 10:52316389-52316389 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.386C>T; p.P129L; 10:52315065-52315065 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.694G>T; p.E232*; 10:52316700-52316700 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.621C>T; p.S207S; 10:52316627-52316627 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.694G>T; p.E232*; 10:52316700-52316700 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.93C>A; p.A31A; 10:52314527-52314527 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.300C>A; p.P100P; 10:52314979-52314979 |
autonomic_ganglia | neuroblastoma | Substitution - coding silent |
c.211G>A; p.G71R; 10:52314645-52314645 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.121G>A; p.A41T; 10:52314555-52314555 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.121G>A; p.A41T; 10:52314555-52314555 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.711T>A; p.C237*; 10:52316717-52316717 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.373G>A; p.A125T; 10:52315052-52315052 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.152G>A; p.G51D; 10:52314586-52314586 |
skin | malignant_melanoma | Substitution - Missense |
c.15C>T; p.G5G; 10:52314449-52314449 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.158C>T; p.A53V; 10:52314592-52314592 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.672G>C; p.R224S; 10:52316678-52316678 |
upper_aerodigestive_tract; larynx | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.205C>T; p.P69S; 10:52314639-52314639 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.572G>T; p.R191L; 10:52316578-52316578 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.292G>A; p.A98T; 10:52314971-52314971 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.620C>A; p.S207Y; 10:52316626-52316626 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.230T>C; p.I77T; 10:52314664-52314664 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.85G>T; p.V29L; 10:52314519-52314519 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.527C>A; p.S176*; 10:52316415-52316415 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.707G>A; p.R236H; 10:52316713-52316713 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.391A>C; p.N131H; 10:52315070-52315070 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.668A>G; p.H223R; 10:52316674-52316674 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.668A>G; p.H223R; 10:52316674-52316674 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.552A>C; p.Q184H; 10:52316558-52316558 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.759A>T; p.Q253H; 10:52316765-52316765 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.139C>A; p.P47T; 10:52314573-52314573 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.29C>A; p.T10N; 10:52314463-52314463 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.138C>T; p.P46P; 10:52314572-52314572 |
skin | malignant_melanoma | Substitution - coding silent |
c.367C>T; p.R123C; 10:52315046-52315046 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.109C>T; p.L37F; 10:52314543-52314543 |
skin | malignant_melanoma | Substitution - Missense |
c.189G>A; p.A63A; 10:52314623-52314623 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.316G>A; p.A106T; 10:52314995-52314995 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.372C>T; p.H124H; 10:52315051-52315051 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.368G>A; p.R123H; 10:52315047-52315047 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.442_443GG>AA; p.G148K; 10:52316330-52316331 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.680G>A; p.G227D; 10:52316686-52316686 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.244-7C>T; p.?; 10:52314916-52314916 |
breast | carcinoma | Unknown |
c.673A>G; p.R225G; 10:52316679-52316679 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.619T>C; p.S207P; 10:52316625-52316625 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.221A>G; p.Y74C; 10:52314655-52314655 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |