| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 11320 |
Name | MGAT4A |
Synonymous | mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme A;MGAT4A;mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme A |
Definition | N-acetylglucosaminyltransferase IVa|N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase IVa|UDP-GlcNAc:a-1,3-D-mannoside b-1,4-acetylglucosaminyltransferase IV|UDP-N-acetylglucosamine: alpha-1,3-D-mannoside beta-1,4-N-acetylglucosaminy |
Position | 2q12 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.866A>G; p.E289G; 2:98645451-98645451 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.243T>G; p.D81E; 2:98678323-98678323 |
skin | malignant_melanoma | Substitution - Missense |
c.401G>T; p.G134V; 2:98675037-98675037 |
skin | malignant_melanoma | Substitution - Missense |
c.1461C>T; p.F487F; 2:98635229-98635229 |
skin | malignant_melanoma | Substitution - coding silent |
c.37G>T; p.A13S; 2:98726296-98726296 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.692G>A; p.R231K; 2:98656358-98656358 |
skin | malignant_melanoma | Substitution - Missense |
c.212G>T; p.R71L; 2:98678354-98678354 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.59delC; p.T20fs*15; 2:98726274-98726274 |
large_intestine; rectum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.332A>C; p.H111P; 2:98675106-98675106 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1243G>A; p.E415K; 2:98639887-98639887 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.407C>T; p.S136L; 2:98663176-98663176 |
skin | malignant_melanoma | Substitution - Missense |
c.1174C>A; p.P392T; 2:98639956-98639956 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.146G>A; p.R49Q; 2:98678420-98678420 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.70T>G; p.Y24D; 2:98726263-98726263 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.822A>C; p.K274N; 2:98645495-98645495 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.116G>A; p.R39Q; 2:98678450-98678450 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.22G>T; p.V8L; 2:98726311-98726311 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.207C>G; p.F69L; 2:98678359-98678359 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.985C>A; p.L329I; 2:98643958-98643958 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1164C>T; p.I388I; 2:98639966-98639966 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1535G>T; p.R512L; 2:98625769-98625769 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1279G>T; p.D427Y; 2:98639851-98639851 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.414C>T; p.V138V; 2:98663169-98663169 |
central_nervous_system; brain | glioma | Substitution - coding silent |
c.1036_1039delCAGA; p.Q346fs*35; 2:98640210-98640213 |
breast | carcinoma | Deletion - Frameshift |
c.501G>T; p.E167D; 2:98663082-98663082 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.403+3A>G; p.?; 2:98675032-98675032 |
stomach | adenocarcinoma | Unknown |
c.1469G>A; p.G490E; 2:98625835-98625835 |
NS | malignant_melanoma | Substitution - Missense |
c.123C>T; p.F41F; 2:98678443-98678443 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1058G>A; p.R353H; 2:98640191-98640191 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.609C>T; p.G203G; 2:98656441-98656441 |
breast | carcinoma | Substitution - coding silent |
c.1021-1G>T; p.?; 2:98640229-98640229 |
liver | carcinoma | Unknown |
c.1021-1G>T; p.?; 2:98640229-98640229 |
liver | carcinoma | Unknown |
c.1117delC; p.Q373fs*9; 2:98640132-98640132 |
liver | carcinoma; hepatocellular_carcinoma | Deletion - Frameshift |
c.1475T>G; p.F492C; 2:98625829-98625829 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1185G>T; p.E395D; 2:98639945-98639945 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.124C>T; p.L42F; 2:98678442-98678442 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.88G>C; p.G30R; 2:98726245-98726245 |
breast | carcinoma | Substitution - Missense |
c.906G>A; p.A302A; 2:98644037-98644037 |
stomach | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1444T>G; p.L482V; 2:98635246-98635246 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.906G>A; p.A302A; 2:98644037-98644037 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.906G>A; p.A302A; 2:98644037-98644037 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.211C>A; p.R71S; 2:98678355-98678355 |
liver | carcinoma | Substitution - Missense |
c.842C>T; p.S281F; 2:98645475-98645475 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.305C>T; p.S102F; 2:98675133-98675133 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.192G>A; p.T64T; 2:98678374-98678374 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.94+6G>A; p.?; 2:98726233-98726233 |
liver | carcinoma; hepatocellular_carcinoma | Unknown |
c.818T>C; p.I273T; 2:98645499-98645499 |
breast | carcinoma | Substitution - Missense |
c.1165C>T; p.H389Y; 2:98639965-98639965 |
skin | malignant_melanoma | Substitution - Missense |
c.579G>A; p.E193E; 2:98658223-98658223 |
breast | carcinoma | Substitution - coding silent |
c.1565_1566GG>AA; p.W522*; 2:98625738-98625739 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |
c.348G>A; p.L116L; 2:98675090-98675090 |
skin | malignant_melanoma | Substitution - coding silent |
c.626C>T; p.S209L; 2:98656424-98656424 |
skin | malignant_melanoma | Substitution - Missense |
c.403G>A; p.V135I; 2:98675035-98675035 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.605C>A; p.S202Y; 2:98656445-98656445 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.825T>A; p.N275K; 2:98645492-98645492 |
oesophagus | carcinoma | Substitution - Missense |
c.985C>T; p.L329F; 2:98643958-98643958 |
skin | malignant_melanoma | Substitution - Missense |
c.1340G>A; p.G447D; 2:98636578-98636578 |
breast | carcinoma | Substitution - Missense |
c.923T>C; p.I308T; 2:98644020-98644020 |
salivary_gland; parotid | carcinoma; adenoid_cystic_carcinoma | Substitution - Missense |
c.409A>G; p.I137V; 2:98663174-98663174 |
liver | carcinoma | Substitution - Missense |
c.409A>G; p.I137V; 2:98663174-98663174 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.1052G>A; p.R351Q; 2:98640197-98640197 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.307C>G; p.L103V; 2:98675131-98675131 |
stomach | adenocarcinoma | Substitution - Missense |
c.548A>T; p.D183V; 2:98658254-98658254 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1124T>C; p.L375P; 2:98640125-98640125 |
skin; upper_arm | malignant_melanoma | Substitution - Missense |
c.255G>A; p.K85K; 2:98678311-98678311 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.50C>T; p.S17F; 2:98726283-98726283 |
skin | malignant_melanoma | Substitution - Missense |
c.468T>G; p.L156L; 2:98663115-98663115 |
breast | carcinoma | Substitution - coding silent |
c.508G>T; p.D170Y; 2:98663075-98663075 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1521C>T; p.P507P; 2:98625783-98625783 |
breast | carcinoma | Substitution - coding silent |
c.277C>A; p.L93M; 2:98675161-98675161 |
liver | carcinoma | Substitution - Missense |
c.1442G>A; p.R481Q; 2:98635248-98635248 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1442G>A; p.R481Q; 2:98635248-98635248 |
oesophagus | carcinoma | Substitution - Missense |
c.1442G>A; p.R481Q; 2:98635248-98635248 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1442G>A; p.R481Q; 2:98635248-98635248 |
skin | malignant_melanoma | Substitution - Missense |
c.1177C>T; p.P393S; 2:98639953-98639953 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1258G>A; p.A420T; 2:98639872-98639872 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.322A>G; p.I108V; 2:98675116-98675116 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.99delA; p.K33fs*2; 2:98678467-98678467 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.1398delT; p.F466fs*8; 2:98636520-98636520 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.715A>C; p.N239H; 2:98655504-98655504 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.987C>T; p.L329L; 2:98643956-98643956 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.115C>T; p.R39*; 2:98678451-98678451 |
stomach | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.249G>C; p.L83F; 2:98678317-98678317 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.683C>T; p.S228F; 2:98656367-98656367 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.1209C>T; p.Y403Y; 2:98639921-98639921 |
skin | malignant_melanoma | Substitution - coding silent |