Pulmonary Arterial Hypertension KnowledgeBase (bioinfom_tsdb)
bioinfom_tsdb
Pulmonary Arterial Hypertension KnowledgeBase
General information | Literature | Expression | Regulation | Variant | Interaction

Basic Information

Gene ID

3621

Name

ING1

Synonymous

inhibitor of growth family, member 1;ING1;inhibitor of growth family, member 1

Definition

growth inhibitor ING1|growth inhibitory protein ING1|inhibitor of growth protein 1|tumor suppressor ING1

Position

13q34

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

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

Top

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

Top

Loss of Function mutations compare to missense mutation.
The ratio of the loss-of-function mutations over missense mutations is 0.34.

The copy number variations for various cancers

Top

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.576C>T; p.A192A; 13:110719668-110719668

lung; middle_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.625G>T; p.E209*; 13:110719717-110719717

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.494A>C; p.N165T; 13:110719586-110719586

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.603C>T; p.A201A; 13:110719695-110719695

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.767G>A; p.C256Y; 13:110719859-110719859

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.253G>A; p.G85S; 13:110719345-110719345

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - Missense

c.700G>A; p.E234K; 13:110719792-110719792

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.763A>T; p.K255*; 13:110719855-110719855

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.585G>C; p.E195D; 13:110719677-110719677

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.679G>T; p.D227Y; 13:110719771-110719771

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.679G>T; p.D227Y; 13:110719771-110719771

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.703T>C; p.W235R; 13:110719795-110719795

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.703T>C; p.W235R; 13:110719795-110719795

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.674G>A; p.G225D; 13:110719766-110719766

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.705G>A; p.W235*; 13:110719797-110719797

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.391G>A; p.A131T; 13:110719483-110719483

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.178C>T; p.R60C; 13:110719270-110719270

oesophaguscarcinomaSubstitution - Missense

c.445C>T; p.R149C; 13:110719537-110719537

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.705G>T; p.W235C; 13:110719797-110719797

ovarycarcinoma; serous_carcinomaSubstitution - Missense

c.740C>A; p.P247H; 13:110719832-110719832

ovarycarcinoma; adenocarcinomaSubstitution - Missense

c.154G>T; p.D52Y; 13:110719246-110719246

autonomic_ganglianeuroblastomaSubstitution - Missense

c.505G>A; p.D169N; 13:110719597-110719597

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.485C>T; p.A162V; 13:110719577-110719577

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.514G>T; p.A172S; 13:110719606-110719606

breastcarcinomaSubstitution - Missense

c.657C>A; p.S219S; 13:110719749-110719749

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.414G>A; p.A138A; 13:110719506-110719506

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.33C>T; p.H11H; 13:110714182-110714182

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.469G>A; p.E157K; 13:110719561-110719561

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.727C>T; p.L243F; 13:110719819-110719819

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.487T>C; p.S163P; 13:110719579-110719579

thyroidother; neoplasmSubstitution - Missense

c.514G>A; p.A172T; 13:110719606-110719606

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.586C>T; p.R196*; 13:110719678-110719678

central_nervous_system; braingliomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

stomachcarcinoma; adenocarcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

stomachcarcinoma; adenocarcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

urinary_tract; bladdercarcinoma; transitional_cell_carcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

urinary_tract; bladdercarcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.586C>T; p.R196*; 13:110719678-110719678

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.507C>T; p.D169D; 13:110719599-110719599

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.513C>T; p.G171G; 13:110719605-110719605

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.513C>T; p.G171G; 13:110719605-110719605

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.230C>T; p.A77V; 13:110719322-110719322

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.512G>A; p.G171D; 13:110719604-110719604

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.345G>A; p.A115A; 13:110719437-110719437

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.305G>A; p.R102H; 13:110719397-110719397

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.274G>A; p.V92M; 13:110719366-110719366

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.305G>A; p.R102H; 13:110719397-110719397

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.202C>T; p.R68W; 13:110719294-110719294

haematopoietic_and_lymphoid_tissuelymphoid_neoplasm; acute_lymphoblastic_leukaemiaSubstitution - Missense

c.273C>T; p.I91I; 13:110719365-110719365

skinmalignant_melanomaSubstitution - coding silent

c.484G>A; p.A162T; 13:110719576-110719576

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.435C>T; p.P145P; 13:110719527-110719527

breastcarcinomaSubstitution - coding silent

c.575C>T; p.A192V; 13:110719667-110719667

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.688G>T; p.E230*; 13:110719780-110719780

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.259G>A; p.E87K; 13:110719351-110719351

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.630C>G; p.P210P; 13:110719722-110719722

lung; right_upper_lobecarcinoma; adenocarcinomaSubstitution - coding silent

c.259G>A; p.E87K; 13:110719351-110719351

breastcarcinomaSubstitution - Missense

c.58C>G; p.L20V; 13:110714207-110714207

breastcarcinomaSubstitution - Missense

c.492C>A; p.S164R; 13:110719584-110719584

central_nervous_system; brainglioma; astrocytoma_Grade_IVSubstitution - Missense

c.777G>A; p.E259E; 13:110719869-110719869

breastcarcinomaSubstitution - coding silent

c.644G>A; p.C215Y; 13:110719736-110719736

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.475C>A; p.R159S; 13:110719567-110719567

skinmalignant_melanomaSubstitution - Missense

c.678C>T; p.C226C; 13:110719770-110719770

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.770G>A; p.R257Q; 13:110719862-110719862

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.770delG; p.E259fs*>21; 13:110719862-110719862

large_intestine; coloncarcinoma; adenocarcinomaDeletion - Frameshift

c.625G>A; p.E209K; 13:110719717-110719717

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.247G>C; p.E83Q; 13:110719339-110719339

breastcarcinomaSubstitution - Missense

c.69C>T; p.I23I; 13:110714218-110714218

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.483C>T; p.N161N; 13:110719575-110719575

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent


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