General information | Literature | Expression | Regulation | Variant | Interaction |
Basic Information |
|
---|---|
Gene ID | 26260 |
Name | FBXO25 |
Synonymous | F-box protein 25;FBXO25;F-box protein 25 |
Definition | F-box only protein 25|F-box protein Fbx25 |
Position | 8p23.3 |
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.465C>T; p.I155I; 8:450073-450073 |
skin | malignant_melanoma | Substitution - coding silent |
c.507C>G; p.I169M; 8:451300-451300 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.357C>A; p.I119I; 8:435683-435683 |
breast | carcinoma | Substitution - coding silent |
c.961C>T; p.R321W; 8:463124-463124 |
breast | carcinoma | Substitution - Missense |
c.735C>T; p.D245D; 8:458443-458443 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.547C>T; p.L183F; 8:451340-451340 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1040C>A; p.A347D; 8:468740-468740 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.121_122delAT; p.I41fs*8; 8:413200-413201 |
pancreas | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.338C>G; p.S113*; 8:435664-435664 |
urinary_tract; bladder | carcinoma | Substitution - Nonsense |
c.570T>C; p.S190S; 8:451363-451363 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.138C>G; p.I46M; 8:431344-431344 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.138C>G; p.I46M; 8:431344-431344 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.497C>A; p.P166H; 8:451290-451290 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.469C>G; p.Q157E; 8:450077-450077 |
cervix | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.657T>A; p.T219T; 8:451450-451450 |
prostate | carcinoma | Substitution - coding silent |
c.1031G>A; p.C344Y; 8:468731-468731 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.357C>T; p.I119I; 8:435683-435683 |
skin | malignant_melanoma | Substitution - coding silent |
c.892T>G; p.L298V; 8:463055-463055 |
liver | carcinoma | Substitution - Missense |
c.624C>T; p.A208A; 8:451417-451417 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.568T>C; p.S190P; 8:451361-451361 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.438G>T; p.K146N; 8:450046-450046 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.616A>G; p.I206V; 8:451409-451409 |
breast | carcinoma | Substitution - Missense |
c.939C>T; p.Y313Y; 8:463102-463102 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.426C>T; p.G142G; 8:450034-450034 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1060A>G; p.T354A; 8:468760-468760 |
liver | carcinoma | Substitution - Missense |
c.597G>A; p.W199*; 8:451390-451390 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.15T>C; p.G5G; 8:413094-413094 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - coding silent |
c.239-1G>T; p.?; 8:432885-432885 |
large_intestine; rectum | carcinoma; adenocarcinoma | Unknown |
c.603C>T; p.C201C; 8:451396-451396 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - coding silent |
c.427G>A; p.V143M; 8:450035-450035 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.988G>T; p.D330Y; 8:467720-467720 |
breast | carcinoma | Substitution - Missense |
c.193delA; p.R67fs*44; 8:431399-431399 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.604C>T; p.R202*; 8:451397-451397 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Nonsense |
c.193delA; p.R67fs*44; 8:431399-431399 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.315A>G; p.E105E; 8:435641-435641 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.570T>A; p.S190S; 8:451363-451363 |
lung | carcinoma; non_small_cell_carcinoma | Substitution - coding silent |
c.1072C>A; p.P358T; 8:468772-468772 |
adrenal_gland; adrenal_gland | adrenal_cortical_carcinoma; functioning | Substitution - Missense |
c.1072C>T; p.P358S; 8:468772-468772 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.470delA; p.K158fs*11; 8:450078-450078 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.399delA; p.K134fs*4; 8:450007-450007 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.399delA; p.K134fs*4; 8:450007-450007 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1015-2A>G; p.?; 8:468713-468713 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Unknown |
c.784C>T; p.L262F; 8:458492-458492 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.833C>A; p.A278D; 8:458541-458541 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.533C>T; p.S178F; 8:451326-451326 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.113G>A; p.R38H; 8:413192-413192 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1087G>A; p.D363N; 8:468787-468787 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.113G>A; p.R38H; 8:413192-413192 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.349C>T; p.Q117*; 8:435675-435675 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.436A>C; p.K146Q; 8:450044-450044 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.517C>G; p.L173V; 8:451310-451310 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.75T>C; p.C25C; 8:413154-413154 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |