| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 84572 |
Name | GNPTG |
Synonymous | N-acetylglucosamine-1-phosphate transferase, gamma subunit;GNPTG;N-acetylglucosamine-1-phosphate transferase, gamma subunit |
Definition | N-acetylglucosamine-1-phosphotransferase subunit gamma|UDP-N-acetylglucosamine-1-phosphotransferase subunit gamma|glcNAc-1-phosphotransferase subunit gamma |
Position | 16p13.3 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.609+10C>T; p.?; 16:1362544-1362544 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Unknown |
c.603C>T; p.T201T; 16:1362528-1362528 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.603C>T; p.T201T; 16:1362528-1362528 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.646G>A; p.A216T; 16:1362647-1362647 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.779A>C; p.K260T; 16:1362862-1362862 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.602delC; p.Q203fs*7; 16:1362527-1362527 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.872C>T; p.S291F; 16:1363045-1363045 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.341C>T; p.A114V; 16:1362061-1362061 |
skin | malignant_melanoma | Substitution - Missense |
c.341C>T; p.A114V; 16:1362061-1362061 |
skin | malignant_melanoma | Substitution - Missense |
c.777G>A; p.L259L; 16:1362860-1362860 |
breast | carcinoma | Substitution - coding silent |
c.201C>G; p.L67L; 16:1361765-1361765 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.874C>T; p.P292S; 16:1363047-1363047 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.489C>T; p.F163F; 16:1362283-1362283 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.489C>T; p.F163F; 16:1362283-1362283 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.305G>A; p.S102N; 16:1361943-1361943 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.699T>C; p.G233G; 16:1362700-1362700 |
large_intestine | carcinoma; adenocarcinoma | Substitution - coding silent |
c.233C>T; p.T78M; 16:1361797-1361797 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.235T>C; p.Y79H; 16:1361873-1361873 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.777G>T; p.L259L; 16:1362860-1362860 |
ovary | carcinoma; serous_carcinoma | Substitution - coding silent |
c.812C>G; p.T271R; 16:1362895-1362895 |
oesophagus; lower_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.211T>C; p.C71R; 16:1361775-1361775 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.557G>A; p.R186Q; 16:1362482-1362482 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.400C>A; p.R134R; 16:1362120-1362120 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.865G>A; p.A289T; 16:1363038-1363038 |
pancreas | carcinoma | Substitution - Missense |
c.865G>A; p.A289T; 16:1363038-1363038 |
pancreas | carcinoma | Substitution - Missense |
c.265G>A; p.V89M; 16:1361903-1361903 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.588C>T; p.A196A; 16:1362513-1362513 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.427G>A; p.G143R; 16:1362221-1362221 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.592G>T; p.E198*; 16:1362517-1362517 |
lung | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.687G>A; p.Q229Q; 16:1362688-1362688 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.425G>A; p.C142Y; 16:1362219-1362219 |
oesophagus; lower_third | carcinoma; adenocarcinoma | Substitution - Missense |
c.405G>A; p.Q135Q; 16:1362125-1362125 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.751G>T; p.E251*; 16:1362834-1362834 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.565G>A; p.D189N; 16:1362490-1362490 |
breast | carcinoma | Substitution - Missense |
c.606C>A; p.P202P; 16:1362531-1362531 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.340G>A; p.A114T; 16:1362060-1362060 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.630G>A; p.R210R; 16:1362631-1362631 |
breast | carcinoma | Substitution - coding silent |
c.676G>A; p.E226K; 16:1362677-1362677 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.114G>A; p.V38V; 16:1352242-1352242 |
biliary_tract; gallbladder | carcinoma; adenocarcinoma | Substitution - coding silent |
c.798C>T; p.H266H; 16:1362881-1362881 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.833_838delACTTGG; p.N278_E280>K; 16:1363006-1363011 |
lung | carcinoma; adenocarcinoma | Complex - deletion inframe |
c.638T>G; p.F213C; 16:1362639-1362639 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.197G>A; p.R66Q; 16:1361761-1361761 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.455C>G; p.S152C; 16:1362249-1362249 |
breast | carcinoma | Substitution - Missense |
c.516C>T; p.H172H; 16:1362310-1362310 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |