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

Basic Information

Gene ID

9486

Name

CHST10

Synonymous

carbohydrate sulfotransferase 10;CHST10;carbohydrate sulfotransferase 10

Definition

HNK-1 sulfotransferase|huHNK-1ST

Position

2q11.2

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

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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 0.13.

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.961G>T; p.E321*; 2:100393355-100393355

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Nonsense

c.27C>T; p.A9A; 2:100406649-100406649

large_intestinecarcinoma; adenocarcinomaSubstitution - coding silent

c.498G>A; p.R166R; 2:100395544-100395544

lungcarcinoma; adenocarcinomaSubstitution - coding silent

c.498G>A; p.R166R; 2:100395544-100395544

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - coding silent

c.235C>A; p.L79M; 2:100398100-100398100

livercarcinomaSubstitution - Missense

c.235C>A; p.L79M; 2:100398100-100398100

livercarcinomaSubstitution - Missense

c.535T>A; p.L179M; 2:100393781-100393781

prostatecarcinoma; adenocarcinomaSubstitution - Missense

c.720C>T; p.F240F; 2:100393596-100393596

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.720C>T; p.F240F; 2:100393596-100393596

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.720C>T; p.F240F; 2:100393596-100393596

skinmalignant_melanomaSubstitution - coding silent

c.251G>A; p.R84H; 2:100398084-100398084

oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.686G>A; p.R229Q; 2:100393630-100393630

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.561T>C; p.I187I; 2:100393755-100393755

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.317C>T; p.S106F; 2:100398018-100398018

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.107G>A; p.S36N; 2:100402649-100402649

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.107G>A; p.S36N; 2:100402649-100402649

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.276C>A; p.C92*; 2:100398059-100398059

ovarycarcinoma; serous_carcinomaSubstitution - Nonsense

c.276C>A; p.C92*; 2:100398059-100398059

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Nonsense

c.418G>T; p.V140F; 2:100397917-100397917

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.623G>A; p.R208Q; 2:100393693-100393693

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.733G>A; p.G245S; 2:100393583-100393583

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.877A>G; p.I293V; 2:100393439-100393439

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Missense

c.767T>G; p.F256C; 2:100393549-100393549

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.300C>A; p.L100L; 2:100398035-100398035

skinmalignant_melanomaSubstitution - coding silent

c.742A>T; p.N248Y; 2:100393574-100393574

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.719T>C; p.F240S; 2:100393597-100393597

skinmalignant_melanomaSubstitution - Missense

c.300C>A; p.L100L; 2:100398035-100398035

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.1018G>A; p.E340K; 2:100393298-100393298

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.820G>T; p.E274*; 2:100393496-100393496

kidneycarcinoma; clear_cell_renal_cell_carcinomaSubstitution - Nonsense

c.488G>A; p.G163D; 2:100395554-100395554

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.550A>G; p.K184E; 2:100393766-100393766

haematopoietic_and_lymphoid_tissuelymphoid_neoplasmSubstitution - Missense

c.890C>A; p.A297D; 2:100393426-100393426

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.497G>A; p.R166Q; 2:100395545-100395545

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.702delG; p.I235fs*18; 2:100393614-100393614

large_intestine; rectumcarcinoma; adenocarcinomaDeletion - Frameshift

c.1041G>T; p.G347G; 2:100393275-100393275

central_nervous_system; braingliomaSubstitution - coding silent

c.453C>T; p.I151I; 2:100395589-100395589

skinmalignant_melanomaSubstitution - coding silent

c.15G>A; p.W5*; 2:100406661-100406661

oesophagus; middle_thirdcarcinoma; squamous_cell_carcinomaSubstitution - Nonsense

c.681G>T; p.R227S; 2:100393635-100393635

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.996C>A; p.I332I; 2:100393320-100393320

oesophaguscarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.100+4C>T; p.?; 2:100406572-100406572

pancreascarcinomaUnknown

c.759C>T; p.D253D; 2:100393557-100393557

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.1048A>G; p.K350E; 2:100393268-100393268

skinmalignant_melanomaSubstitution - Missense

c.47T>C; p.F16S; 2:100406629-100406629

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.276C>T; p.C92C; 2:100398059-100398059

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.584_585delTT; p.L195fs*5; 2:100393731-100393732

endometriumcarcinoma; endometrioid_carcinomaDeletion - Frameshift

c.70T>C; p.F24L; 2:100406606-100406606

skinmalignant_melanomaSubstitution - Missense

c.184G>C; p.E62Q; 2:100402572-100402572

skinmalignant_melanomaSubstitution - Missense

c.740C>T; p.P247L; 2:100393576-100393576

lungcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.225C>T; p.L75L; 2:100398110-100398110

skinmalignant_melanomaSubstitution - coding silent

c.389G>T; p.G130V; 2:100397946-100397946

livercarcinomaSubstitution - Missense

c.794C>T; p.T265M; 2:100393522-100393522

lungcarcinoma; small_cell_carcinomaSubstitution - Missense

c.724C>T; p.R242C; 2:100393592-100393592

endometriumcarcinoma; endometrioid_carcinomaSubstitution - Missense

c.736G>A; p.D246N; 2:100393580-100393580

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.844C>T; p.H282Y; 2:100393472-100393472

thyroidcarcinomaSubstitution - Missense

c.1A>G; p.M1V; 2:100406675-100406675

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.721G>A; p.V241M; 2:100393595-100393595

upper_aerodigestive_tract; mouthcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.961G>C; p.E321Q; 2:100393355-100393355

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense

c.568G>T; p.D190Y; 2:100393748-100393748

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.439T>A; p.S147T; 2:100395603-100395603

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.1017C>T; p.F339F; 2:100393299-100393299

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.1017C>T; p.F339F; 2:100393299-100393299

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.110C>T; p.A37V; 2:100402646-100402646

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.275G>T; p.C92F; 2:100398060-100398060

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.577G>A; p.E193K; 2:100393739-100393739

large_intestine; caecumcarcinoma; adenocarcinomaSubstitution - Missense

c.577G>A; p.E193K; 2:100393739-100393739

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.577G>A; p.E193K; 2:100393739-100393739

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.577G>A; p.E193K; 2:100393739-100393739

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.685C>T; p.R229W; 2:100393631-100393631

lungcarcinoma; adenocarcinomaSubstitution - Missense

c.685C>T; p.R229W; 2:100393631-100393631

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.785A>T; p.H262L; 2:100393531-100393531

breastcarcinoma; basal_(triple-negative)_carcinomaSubstitution - Missense

c.850G>A; p.E284K; 2:100393466-100393466

pancreascarcinomaSubstitution - Missense

c.850G>A; p.E284K; 2:100393466-100393466

pancreascarcinomaSubstitution - Missense

c.294G>A; p.K98K; 2:100398041-100398041

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - coding silent

c.870C>T; p.A290A; 2:100393446-100393446

haematopoietic_and_lymphoid_tissuehaematopoietic_neoplasm; acute_myeloid_leukaemiaSubstitution - coding silent

c.77C>T; p.T26M; 2:100406599-100406599

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.77C>T; p.T26M; 2:100406599-100406599

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.918G>A; p.P306P; 2:100393398-100393398

oesophaguscarcinoma; squamous_cell_carcinomaSubstitution - coding silent

c.918G>A; p.P306P; 2:100393398-100393398

thyroidcarcinomaSubstitution - coding silent

c.918G>A; p.P306P; 2:100393398-100393398

endometriumcarcinoma; endometrioid_carcinomaSubstitution - coding silent

c.1001G>A; p.R334H; 2:100393315-100393315

large_intestinecarcinoma; adenocarcinomaSubstitution - Missense

c.929C>T; p.P310L; 2:100393387-100393387

large_intestine; rectumcarcinoma; adenocarcinomaSubstitution - Missense

c.455C>T; p.P152L; 2:100395587-100395587

oesophagus; lower_thirdcarcinoma; adenocarcinomaSubstitution - Missense

c.929C>T; p.P310L; 2:100393387-100393387

skinmalignant_melanomaSubstitution - Missense

c.929C>T; p.P310L; 2:100393387-100393387

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.929C>T; p.P310L; 2:100393387-100393387

stomachcarcinoma; adenocarcinomaSubstitution - Missense

c.1000C>T; p.R334C; 2:100393316-100393316

oesophaguscarcinoma; adenocarcinomaSubstitution - Missense

c.659G>A; p.G220D; 2:100393657-100393657

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.144G>A; p.P48P; 2:100402612-100402612

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - coding silent

c.302C>T; p.S101L; 2:100398033-100398033

large_intestine; coloncarcinoma; adenocarcinomaSubstitution - Missense

c.302C>T; p.S101L; 2:100398033-100398033

skin; head_neckcarcinoma; squamous_cell_carcinomaSubstitution - Missense


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