General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 115761 |
Name | ARL11 |
Synonymous | ADP-ribosylation factor-like 11;ARL11;ADP-ribosylation factor-like 11 |
Definition | ADP-ribosylation factor-like protein 11|ADP-ribosylation factor-like tumor suppressor protein 1 |
Position | 13q14.2 |
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 0.16. |
The copy number variations for various cancers | Top |
There is no record for ARL11 |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) |
Site |
Histology |
Mutation Type |
---|---|---|---|
c.80C>T; p.T27M; 13:49630527-49630527 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.80C>T; p.T27M; 13:49630527-49630527 |
large_intestine; colon | NS | Substitution - Missense |
c.32C>T; p.A11V; 13:49630479-49630479 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.192_193insG; p.Q67fs*27; 13:49630639-49630640 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.216C>A; p.A72A; 13:49630663-49630663 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.343G>A; p.V115I; 13:49630790-49630790 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.343G>A; p.V115I; 13:49630790-49630790 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.226G>A; p.D76N; 13:49630673-49630673 |
breast | carcinoma | Substitution - Missense |
c.198G>A; p.G66G; 13:49630645-49630645 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.544C>T; p.Q182*; 13:49630991-49630991 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.284G>A; p.R95H; 13:49630731-49630731 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.284G>A; p.R95H; 13:49630731-49630731 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.388C>G; p.L130V; 13:49630835-49630835 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.181C>A; p.L61I; 13:49630628-49630628 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.262C>A; p.L88M; 13:49630709-49630709 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.262C>A; p.L88M; 13:49630709-49630709 |
large_intestine; colon | carcinoma | Substitution - Missense |
c.262C>A; p.L88M; 13:49630709-49630709 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.299C>T; p.A100V; 13:49630746-49630746 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.526C>T; p.R176C; 13:49630973-49630973 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.510G>A; p.W170*; 13:49630957-49630957 |
NS | malignant_melanoma | Substitution - Nonsense |
c.510G>A; p.W170*; 13:49630957-49630957 |
NS | malignant_melanoma | Substitution - Nonsense |
c.187G>A; p.D63N; 13:49630634-49630634 |
skin | malignant_melanoma | Substitution - Missense |
c.201G>T; p.Q67H; 13:49630648-49630648 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.46G>T; p.V16L; 13:49630493-49630493 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.190G>A; p.V64I; 13:49630637-49630637 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.265G>A; p.D89N; 13:49630712-49630712 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.297G>A; p.S99S; 13:49630744-49630744 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.297G>A; p.S99S; 13:49630744-49630744 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.297G>A; p.S99S; 13:49630744-49630744 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - coding silent |
c.193delG; p.Q67fs*41; 13:49630640-49630640 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.392C>T; p.P131L; 13:49630839-49630839 |
thyroid | other; neoplasm | Substitution - Missense |
c.249C>T; p.I83I; 13:49630696-49630696 |
skin | malignant_melanoma | Substitution - coding silent |
c.33G>A; p.A11A; 13:49630480-49630480 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.530G>A; p.S177N; 13:49630977-49630977 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.258C>T; p.Y86Y; 13:49630705-49630705 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.253G>A; p.V85M; 13:49630700-49630700 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.40C>A; p.Q14K; 13:49630487-49630487 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.290C>T; p.P97L; 13:49630737-49630737 |
skin | malignant_melanoma | Substitution - Missense |
c.454C>T; p.R152W; 13:49630901-49630901 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.369G>A; p.K123K; 13:49630816-49630816 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.369G>A; p.K123K; 13:49630816-49630816 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.50T>C; p.M17T; 13:49630497-49630497 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.490G>A; p.E164K; 13:49630937-49630937 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.252C>A; p.L84L; 13:49630699-49630699 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.324C>T; p.N108N; 13:49630771-49630771 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.325G>A; p.D109N; 13:49630772-49630772 |
skin | malignant_melanoma | Substitution - Missense |
c.325G>A; p.D109N; 13:49630772-49630772 |
skin | malignant_melanoma | Substitution - Missense |
c.68C>T; p.A23V; 13:49630515-49630515 |
breast | carcinoma | Substitution - Missense |
c.446G>A; p.W149*; 13:49630893-49630893 |
thyroid | other; neoplasm | Substitution - Nonsense |
c.177G>A; p.L59L; 13:49630624-49630624 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |