| Gene ID | 2524 |
| Symbol | FUT2 |
| Synonymous | B12QTL1|SE|SEC2|Se2|sej |
| Full name | fucosyltransferase 2 (secretor status included) |
| Gene description | GDP-L-fucose:beta-D-galactoside 2-alpha-L-fucosyltransferase 2|alpha (1,2) fucosyltransferase|alpha(1,2)FT 2|alpha(1,2)FT2|galactoside 2-alpha-L-fucosyltransferase 2|secretor blood group alpha-2-fucosyltransferase|secretor factor |
| Cytoband | 19q13.3 |
| Gene type | protein-coding |
| Synonymous | MIM:182100; HGNC:HGNC:4013; Ensembl:ENSG00000176920; HPRD:01629; Vega:OTTHUMG00000164427 |
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.772G>A; p.G258S; 19:48703728-48703728 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.478C>A; p.L160I; 19:48703434-48703434 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.662G>T; p.R221L; 19:48703618-48703618 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.870G>A; p.T290T; 19:48703826-48703826 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.249C>T; p.Y83Y; 19:48703205-48703205 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.249C>T; p.Y83Y; 19:48703205-48703205 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.64G>A; p.V22I; 19:48703020-48703020 |
skin | malignant_melanoma | Substitution - Missense |
c.418A>T; p.I140F; 19:48703374-48703374 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.577G>A; p.G193S; 19:48703533-48703533 |
skin | malignant_melanoma | Substitution - Missense |
c.279C>T; p.A93A; 19:48703235-48703235 |
skin | malignant_melanoma | Substitution - coding silent |
c.62C>T; p.T21M; 19:48703018-48703018 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.444C>G; p.T148T; 19:48703400-48703400 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.194C>T; p.T65M; 19:48703150-48703150 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; acute_lymphoblastic_leukaemia | Substitution - Missense |
c.423G>A; p.P141P; 19:48703379-48703379 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.525G>C; p.R175R; 19:48703481-48703481 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - coding silent |
c.896C>T; p.T299M; 19:48703852-48703852 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.597T>C; p.H199H; 19:48703553-48703553 |
breast | carcinoma | Substitution - coding silent |
c.270G>A; p.G90G; 19:48703226-48703226 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.981G>T; p.L327L; 19:48703937-48703937 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.2T>C; p.M1T; 19:48702958-48702958 |
liver | carcinoma | Substitution - Missense |
c.2T>C; p.M1T; 19:48702958-48702958 |
liver | carcinoma | Substitution - Missense |
c.749G>A; p.R250Q; 19:48703705-48703705 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.89A>T; p.Q30L; 19:48703045-48703045 |
skin | malignant_melanoma | Substitution - Missense |
c.658C>T; p.R220W; 19:48703614-48703614 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.894C>T; p.L298L; 19:48703850-48703850 |
liver | carcinoma | Substitution - coding silent |
c.985G>C; p.E329Q; 19:48703941-48703941 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.894C>T; p.L298L; 19:48703850-48703850 |
liver | carcinoma | Substitution - coding silent |
c.409delT; p.Y137fs*51; 19:48703365-48703365 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Deletion - Frameshift |
c.288G>A; p.P96P; 19:48703244-48703244 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.433G>A; p.V145I; 19:48703389-48703389 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.461G>A; p.W154*; 19:48703417-48703417 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.461G>A; p.W154*; 19:48703417-48703417 |
breast | carcinoma | Substitution - Nonsense |
c.461G>A; p.W154*; 19:48703417-48703417 |
breast | carcinoma | Substitution - Nonsense |
c.243A>G; p.T81T; 19:48703199-48703199 |
central_nervous_system; brain | primitive_neuroectodermal_tumour-medulloblastoma | Substitution - coding silent |
c.461G>A; p.W154*; 19:48703417-48703417 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.461G>A; p.W154*; 19:48703417-48703417 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.46A>T; p.I16F; 19:48703002-48703002 |
thyroid | other; neoplasm | Substitution - Missense |
c.660G>A; p.R220R; 19:48703616-48703616 |
breast | carcinoma | Substitution - coding silent |
c.523C>T; p.R175W; 19:48703479-48703479 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.423delG; p.E143fs*45; 19:48703379-48703379 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.167G>A; p.G56E; 19:48703123-48703123 |
skin | malignant_melanoma | Substitution - Missense |
c.575C>T; p.P192L; 19:48703531-48703531 |
liver | carcinoma | Substitution - Missense |
c.61A>C; p.T21P; 19:48703017-48703017 |
skin | malignant_melanoma | Substitution - Missense |
c.231C>T; p.G77G; 19:48703187-48703187 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.10G>A; p.V4I; 19:48702966-48702966 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.238G>A; p.A80T; 19:48703194-48703194 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.654C>T; p.A218A; 19:48703610-48703610 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.203C>T; p.A68V; 19:48703159-48703159 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.40C>A; p.H14N; 19:48702996-48702996 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.363G>A; p.R121R; 19:48703319-48703319 |
skin | malignant_melanoma | Substitution - coding silent |
c.182G>A; p.R61K; 19:48703138-48703138 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.531G>A; p.E177E; 19:48703487-48703487 |
skin | malignant_melanoma | Substitution - coding silent |
c.349G>A; p.A117T; 19:48703305-48703305 |
bone; extraskeletal | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.344A>C; p.H115P; 19:48703300-48703300 |
kidney | carcinoma; papillary_renal_cell_carcinoma | Substitution - Missense |
c.342G>A; p.L114L; 19:48703298-48703298 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.570C>T; p.S190S; 19:48703526-48703526 |
skin | malignant_melanoma | Substitution - coding silent |
c.570C>T; p.S190S; 19:48703526-48703526 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.873C>T; p.F291F; 19:48703829-48703829 |
prostate | carcinoma; adenocarcinoma | Substitution - coding silent |
c.239C>A; p.A80D; 19:48703195-48703195 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.993A>G; p.T331T; 19:48703949-48703949 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.413G>C; p.R138P; 19:48703369-48703369 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.916C>T; p.L306L; 19:48703872-48703872 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.642delG; p.V216fs*71; 19:48703598-48703598 |
large_intestine; rectum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.353C>T; p.T118M; 19:48703309-48703309 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.204A>G; p.A68A; 19:48703160-48703160 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.175C>T; p.Q59*; 19:48703131-48703131 |
pancreas | carcinoma | Substitution - Nonsense |
c.886G>A; p.A296T; 19:48703842-48703842 |
skin | malignant_melanoma | Substitution - Missense |
c.886G>A; p.A296T; 19:48703842-48703842 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.212G>A; p.R71H; 19:48703168-48703168 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1003G>A; p.A335T; 19:48703959-48703959 |
kidney | carcinoma; renal_cell_carcinoma | Substitution - Missense |
c.948C>T; p.F316F; 19:48703904-48703904 |
skin | malignant_melanoma | Substitution - coding silent |
c.661C>T; p.R221*; 19:48703617-48703617 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Nonsense |
c.390C>T; p.N130N; 19:48703346-48703346 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.425G>A; p.G142E; 19:48703381-48703381 |
skin | malignant_melanoma | Substitution - Missense |
c.390C>T; p.N130N; 19:48703346-48703346 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - coding silent |
c.967G>A; p.E323K; 19:48703923-48703923 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; mantle_cell_lymphoma | Substitution - Missense |
c.670C>A; p.Q224K; 19:48703626-48703626 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |