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

Basic Information

Gene ID

3627

Name

CXCL10

Synonymous

chemokine (C-X-C motif) ligand 10;CXCL10;chemokine (C-X-C motif) ligand 10

Definition

10 kDa interferon gamma-induced protein|C-X-C motif chemokine 10|gamma IP10|gamma-IP10|interferon-inducible cytokine IP-10|protein 10 from interferon (gamma)-induced cell line|small inducible cytokine subfamily B (Cys-X-Cys), member 10|small-inducible cyt

Position

4q21

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 0.00.

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.249G>T; p.K83N; 4:76022395-76022395

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.249G>T; p.K83N; 4:76022395-76022395

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.138A>G; p.E46E; 4:76022741-76022741

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.223C>T; p.L75L; 4:76022421-76022421

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.100A>G; p.S34G; 4:76022779-76022779

skinmalignant_melanomaSubstitution - Missense

c.114A>G; p.Q38Q; 4:76022765-76022765

skinmalignant_melanomaSubstitution - coding silent

c.108T>C; p.S36S; 4:76022771-76022771

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - coding silent

c.82G>A; p.V28I; 4:76022797-76022797

breastcarcinomaSubstitution - Missense

c.279G>A; p.R93R; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.279G>A; p.R93R; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.279G>A; p.R93R; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.279G>A; p.R93R; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.279G>A; p.R93R; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.237G>A; p.S79S; 4:76022407-76022407

lungcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.273G>A; p.K91K; 4:76022371-76022371

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.22A>G; p.I8V; 4:76023410-76023410

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.23T>C; p.I8T; 4:76023409-76023409

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.178G>A; p.V60I; 4:76022701-76022701

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.236C>T; p.S79L; 4:76022408-76022408

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.42G>A; p.L14L; 4:76023390-76023390

stomachcarcinoma; adenocarcinomaSubstitution - coding silent

c.236C>T; p.S79L; 4:76022408-76022408

skinmalignant_melanomaSubstitution - Missense

c.279G>T; p.R93S; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.279G>T; p.R93S; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.279G>T; p.R93S; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.279G>T; p.R93S; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.279G>T; p.R93S; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.279G>T; p.R93S; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.279G>T; p.R93S; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.279G>T; p.R93S; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense

c.292C>T; p.P98S; 4:76021935-76021935

skinmalignant_melanomaSubstitution - Missense

c.275A>T; p.E92V; 4:76022369-76022369

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.69T>A; p.P23P; 4:76022810-76022810

pancreascarcinomaSubstitution - coding silent

c.61G>A; p.G21R; 4:76023371-76023371

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.279G>C; p.R93S; 4:76021948-76021948

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - Missense


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