| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 50515 |
Name | CHST11 |
Synonymous | carbohydrate (chondroitin 4) sulfotransferase 11;CHST11;carbohydrate (chondroitin 4) sulfotransferase 11 |
Definition | C4S-1|IgH/CHST11 fusion|carbohydrate sulfotransferase 11|chondroitin 4-O-sulfotransferase 1 |
Position | 12q |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.656G>A; p.R219H; 12:104757400-104757400 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.704T>A; p.V235D; 12:104757448-104757448 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.369G>T; p.V123V; 12:104757113-104757113 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.469G>T; p.V157F; 12:104757213-104757213 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.814C>T; p.H272Y; 12:104757558-104757558 |
skin | malignant_melanoma | Substitution - Missense |
c.993C>T; p.Y331Y; 12:104757737-104757737 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.5A>C; p.K2T; 12:104457416-104457416 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.503G>A; p.S168N; 12:104757247-104757247 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.451C>T; p.P151S; 12:104757195-104757195 |
skin; scalp | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.336G>A; p.V112V; 12:104757080-104757080 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.402C>T; p.L134L; 12:104757146-104757146 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.661C>T; p.R221W; 12:104757405-104757405 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.547C>T; p.L183L; 12:104757291-104757291 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.661C>T; p.R221W; 12:104757405-104757405 |
large_intestine; colon | adenoma | Substitution - Missense |
c.179T>A; p.L60Q; 12:104601966-104601966 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.852G>T; p.E284D; 12:104757596-104757596 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.473C>A; p.S158Y; 12:104757217-104757217 |
prostate | carcinoma | Substitution - Missense |
c.84G>A; p.L28L; 12:104457495-104457495 |
stomach | carcinoma; diffuse_adenocarcinoma | Substitution - coding silent |
c.524G>A; p.R175H; 12:104757268-104757268 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.865G>A; p.V289I; 12:104757609-104757609 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.348C>T; p.H116H; 12:104757092-104757092 |
prostate | carcinoma | Substitution - coding silent |
c.125G>T; p.R42L; 12:104601912-104601912 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.348C>T; p.H116H; 12:104757092-104757092 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.840G>C; p.E280D; 12:104757584-104757584 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.559G>A; p.E187K; 12:104757303-104757303 |
skin | malignant_melanoma | Substitution - Missense |
c.600C>T; p.F200F; 12:104757344-104757344 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.759G>T; p.E253D; 12:104757503-104757503 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1000T>C; p.Y334H; 12:104757744-104757744 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.475G>A; p.A159T; 12:104757219-104757219 |
breast | carcinoma | Substitution - Missense |
c.475G>A; p.A159T; 12:104757219-104757219 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.475G>A; p.A159T; 12:104757219-104757219 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.475G>A; p.A159T; 12:104757219-104757219 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.475G>A; p.A159T; 12:104757219-104757219 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.475G>A; p.A159T; 12:104757219-104757219 |
pancreas | carcinoma | Substitution - Missense |
c.1008C>T; p.L336L; 12:104757752-104757752 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.284C>A; p.T95K; 12:104757028-104757028 |
thyroid | other; neoplasm | Substitution - Missense |
c.905C>T; p.P302L; 12:104757649-104757649 |
skin | malignant_melanoma | Substitution - Missense |
c.81C>A; p.I27I; 12:104457492-104457492 |
thyroid | carcinoma | Substitution - coding silent |
c.553G>C; p.V185L; 12:104757297-104757297 |
pancreas | carcinoma | Substitution - Missense |
c.469G>A; p.V157I; 12:104757213-104757213 |
stomach | adenocarcinoma | Substitution - Missense |
c.170G>A; p.R57Q; 12:104601957-104601957 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.170G>A; p.R57Q; 12:104601957-104601957 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.781A>C; p.T261P; 12:104757525-104757525 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.525C>A; p.R175R; 12:104757269-104757269 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.525C>A; p.R175R; 12:104757269-104757269 |
oesophagus | carcinoma; adenocarcinoma | Substitution - coding silent |
c.857C>T; p.S286F; 12:104757601-104757601 |
pancreas | carcinoma | Substitution - Missense |
c.398G>A; p.R133Q; 12:104757142-104757142 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.398G>A; p.R133Q; 12:104757142-104757142 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.700G>A; p.D234N; 12:104757444-104757444 |
skin | malignant_melanoma | Substitution - Missense |
c.521A>G; p.H174R; 12:104757265-104757265 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.769G>A; p.E257K; 12:104757513-104757513 |
pancreas | carcinoma | Substitution - Missense |
c.315C>G; p.N105K; 12:104757059-104757059 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.715G>T; p.E239*; 12:104757459-104757459 |
liver | carcinoma | Substitution - Nonsense |
c.93C>G; p.F31L; 12:104457504-104457504 |
skin | malignant_melanoma | Substitution - Missense |
c.590G>A; p.R197H; 12:104757334-104757334 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.474C>T; p.S158S; 12:104757218-104757218 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.937G>A; p.E313K; 12:104757681-104757681 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.825C>T; p.L275L; 12:104757569-104757569 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.897G>A; p.L299L; 12:104757641-104757641 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.455C>T; p.A152V; 12:104757199-104757199 |
skin | malignant_melanoma | Substitution - Missense |
c.751C>T; p.R251W; 12:104757495-104757495 |
breast | carcinoma | Substitution - Missense |
c.714G>T; p.E238D; 12:104757458-104757458 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.211C>T; p.L71F; 12:104756955-104756955 |
haematopoietic_and_lymphoid_tissue; central_nervous_system | lymphoid_neoplasm; primary_central_nervous_system_lymphoma | Substitution - Missense |
c.798C>T; p.C266C; 12:104757542-104757542 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.411C>T; p.V137V; 12:104757155-104757155 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.800A>C; p.H267P; 12:104757544-104757544 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - Missense |
c.705C>G; p.V235V; 12:104757449-104757449 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.669C>T; p.N223N; 12:104757413-104757413 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.191A>G; p.Y64C; 12:104601978-104601978 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.175C>T; p.P59S; 12:104601962-104601962 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.417C>T; p.T139T; 12:104757161-104757161 |
breast | carcinoma | Substitution - coding silent |
c.985C>T; p.Q329*; 12:104757729-104757729 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.837C>G; p.Y279*; 12:104757581-104757581 |
skin | malignant_melanoma | Substitution - Nonsense |
c.662G>A; p.R221Q; 12:104757406-104757406 |
autonomic_ganglia | neuroblastoma | Substitution - Missense |
c.662G>A; p.R221Q; 12:104757406-104757406 |
liver | carcinoma | Substitution - Missense |
c.83T>G; p.L28R; 12:104457494-104457494 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.125G>A; p.R42Q; 12:104601912-104601912 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.1026T>G; p.N342K; 12:104757770-104757770 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.125G>A; p.R42Q; 12:104601912-104601912 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.801T>C; p.H267H; 12:104757545-104757545 |
thyroid | other; neoplasm | Substitution - coding silent |
c.992A>G; p.Y331C; 12:104757736-104757736 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.864C>T; p.Y288Y; 12:104757608-104757608 |
breast | carcinoma | Substitution - coding silent |
c.864C>T; p.Y288Y; 12:104757608-104757608 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.349G>A; p.E117K; 12:104757093-104757093 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.296G>A; p.R99Q; 12:104757040-104757040 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.645G>T; p.K215N; 12:104757389-104757389 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.468C>T; p.H156H; 12:104757212-104757212 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.711C>T; p.F237F; 12:104757455-104757455 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.994G>A; p.E332K; 12:104757738-104757738 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.711C>T; p.F237F; 12:104757455-104757455 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.994G>A; p.E332K; 12:104757738-104757738 |
skin | malignant_melanoma | Substitution - Missense |
c.568G>A; p.E190K; 12:104757312-104757312 |
skin | malignant_melanoma | Substitution - Missense |
c.468C>T; p.H156H; 12:104757212-104757212 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.711C>T; p.F237F; 12:104757455-104757455 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.994G>A; p.E332K; 12:104757738-104757738 |
oesophagus | carcinoma | Substitution - Missense |
c.711C>T; p.F237F; 12:104757455-104757455 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.480C>T; p.N160N; 12:104757224-104757224 |
skin | malignant_melanoma | Substitution - coding silent |
c.1028A>G; p.Y343C; 12:104757772-104757772 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.269G>A; p.R90Q; 12:104757013-104757013 |
skin | malignant_melanoma | Substitution - Missense |
c.269G>A; p.R90Q; 12:104757013-104757013 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.913G>A; p.A305T; 12:104757657-104757657 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.397C>T; p.R133W; 12:104757141-104757141 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.567C>T; p.F189F; 12:104757311-104757311 |
bone; rib | chondrosarcoma | Substitution - coding silent |
c.567C>T; p.F189F; 12:104757311-104757311 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.241C>T; p.R81W; 12:104756985-104756985 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |