Pulmonary Arterial Hypertension KnowledgeBase (bioinfom_tsdb)
bioinfom_tsdb
Pulmonary Arterial Hypertension KnowledgeBase
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

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We used uniprot protein structure data from ensemble BioMart database. The size of circle shows the relative mutation number.

The non-synonymous (top) and synonymous (bottom) mutational percentage for various cancers

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The non-synonymous mutational pattern in 17 major cancer types.
The synonymous mutational pattern in 17 major cancer types.

Loss of Function mutations compare to missense mutations

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Loss of Function mutations compare to missense mutation.
The ratio of the loss-of-function mutations over missense mutations is 0.14.

The copy number variations for various cancers

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The copy number variations in 17 major cancer groups: 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; NS, 11; Ovary, 12; Pancreas, 13; Prostate, 14; Skin, 15; Stomach, 16; Thyroid, 17; Urinary tract

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

skinmalignant_melanomaSubstitution - coding silent

c.507C>G; p.I169M; 8:451300-451300

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.357C>A; p.I119I; 8:435683-435683

breastcarcinomaSubstitution - coding silent

c.961C>T; p.R321W; 8:463124-463124

breastcarcinomaSubstitution - Missense

c.735C>T; p.D245D; 8:458443-458443

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.547C>T; p.L183F; 8:451340-451340

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.1040C>A; p.A347D; 8:468740-468740

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.121_122delAT; p.I41fs*8; 8:413200-413201

pancreascarcinoma; adenocarcinomaDeletion - Frameshift

c.338C>G; p.S113*; 8:435664-435664

urinary_tract; bladdercarcinomaSubstitution - Nonsense

c.570T>C; p.S190S; 8:451363-451363

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.138C>G; p.I46M; 8:431344-431344

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.138C>G; p.I46M; 8:431344-431344

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.497C>A; p.P166H; 8:451290-451290

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.469C>G; p.Q157E; 8:450077-450077

cervixcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.657T>A; p.T219T; 8:451450-451450

prostatecarcinomaSubstitution - coding silent

c.1031G>A; p.C344Y; 8:468731-468731

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.357C>T; p.I119I; 8:435683-435683

skinmalignant_melanomaSubstitution - coding silent

c.892T>G; p.L298V; 8:463055-463055

livercarcinomaSubstitution - Missense

c.624C>T; p.A208A; 8:451417-451417

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.568T>C; p.S190P; 8:451361-451361

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.438G>T; p.K146N; 8:450046-450046

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.616A>G; p.I206V; 8:451409-451409

breastcarcinomaSubstitution - Missense

c.939C>T; p.Y313Y; 8:463102-463102

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.426C>T; p.G142G; 8:450034-450034

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.1060A>G; p.T354A; 8:468760-468760

livercarcinomaSubstitution - Missense

c.597G>A; p.W199*; 8:451390-451390

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.15T>C; p.G5G; 8:413094-413094

oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - coding silent

c.239-1G>T; p.?; 8:432885-432885

large_intestine; rectumcarcinoma; adenocarcinomaUnknown

c.603C>T; p.C201C; 8:451396-451396

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.427G>A; p.V143M; 8:450035-450035

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.988G>T; p.D330Y; 8:467720-467720

breastcarcinomaSubstitution - Missense

c.193delA; p.R67fs*44; 8:431399-431399

large_intestine; caecumcarcinoma; adenocarcinomaDeletion - Frameshift

c.604C>T; p.R202*; 8:451397-451397

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.193delA; p.R67fs*44; 8:431399-431399

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.315A>G; p.E105E; 8:435641-435641

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.570T>A; p.S190S; 8:451363-451363

lungcarcinoma; non_small_cell_carcinomaSubstitution - coding silent

c.1072C>A; p.P358T; 8:468772-468772

adrenal_gland; adrenal_glandadrenal_cortical_carcinoma; functioningSubstitution - Missense

c.1072C>T; p.P358S; 8:468772-468772

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.470delA; p.K158fs*11; 8:450078-450078

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.399delA; p.K134fs*4; 8:450007-450007

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.399delA; p.K134fs*4; 8:450007-450007

large_intestinecarcinoma; adenocarcinomaDeletion - Frameshift

c.1015-2A>G; p.?; 8:468713-468713

oesophagus; lower_thirdcarcinoma; squamous_cell_carcinomaUnknown

c.784C>T; p.L262F; 8:458492-458492

haematopoietic_and_lymphoid_tissue; central_nervous_systemlymphoid_neoplasm; primary_central_nervous_system_lymphomaSubstitution - Missense

c.833C>A; p.A278D; 8:458541-458541

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.533C>T; p.S178F; 8:451326-451326

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.113G>A; p.R38H; 8:413192-413192

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.1087G>A; p.D363N; 8:468787-468787

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.113G>A; p.R38H; 8:413192-413192

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.349C>T; p.Q117*; 8:435675-435675

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.436A>C; p.K146Q; 8:450044-450044

oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.517C>G; p.L173V; 8:451310-451310

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.75T>C; p.C25C; 8:413154-413154

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent


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