| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 7293 |
Name | TNFRSF4 |
Synonymous | tumor necrosis factor receptor superfamily, member 4;TNFRSF4;tumor necrosis factor receptor superfamily, member 4 |
Definition | ACT35 antigen|ATC35 antigen|CD134 antigen|OX40 antigen|OX40 cell surface antigen|OX40 homologue|OX40L receptor|TAX transcriptionally-activated glycoprotein 1 receptor|lymphoid activation antigene ACT35|tax-transcriptionally activated glycoprotein 1 recept |
Position | 1p36 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.515delC; p.P172fs*>106; 1:1212061-1212061 |
large_intestine; caecum | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.515delC; p.P172fs*>106; 1:1212061-1212061 |
large_intestine; colon | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.28C>T; p.R10C; 1:1214100-1214100 |
thyroid | other; neoplasm | Substitution - Missense |
c.337A>C; p.T113P; 1:1213025-1213025 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.502G>A; p.D168N; 1:1212074-1212074 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.337A>C; p.T113P; 1:1213025-1213025 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.490G>A; p.A164T; 1:1212086-1212086 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.312C>T; p.D104D; 1:1213050-1213050 |
lung | carcinoma; adenocarcinoma | Substitution - coding silent |
c.765G>A; p.G255G; 1:1211624-1211624 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - coding silent |
c.201C>T; p.C67C; 1:1213730-1213730 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.9G>T; p.V3V; 1:1214119-1214119 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - coding silent |
c.163C>T; p.R55C; 1:1213768-1213768 |
bone | Ewings_sarcoma-peripheral_primitive_neuroectodermal_tumour | Substitution - Missense |
c.487G>A; p.D163N; 1:1212089-1212089 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.43G>A; p.A15T; 1:1214085-1214085 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.525G>A; p.Q175Q; 1:1212051-1212051 |
skin | malignant_melanoma | Substitution - coding silent |
c.630C>A; p.P210P; 1:1211946-1211946 |
liver | carcinoma | Substitution - coding silent |
c.641C>T; p.A214V; 1:1211826-1211826 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.745G>A; p.D249N; 1:1211722-1211722 |
skin | malignant_melanoma | Substitution - Missense |
c.745G>A; p.D249N; 1:1211722-1211722 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.745G>A; p.D249N; 1:1211722-1211722 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.745G>A; p.D249N; 1:1211722-1211722 |
stomach | carcinoma; intestinal_adenocarcinoma | Substitution - Missense |
c.548_549insC; p.A184fs*10; 1:1212027-1212028 |
large_intestine; colon | carcinoma; adenocarcinoma | Insertion - Frameshift |
c.534G>A; p.E178E; 1:1212042-1212042 |
thyroid | other; neoplasm | Substitution - coding silent |
c.534G>A; p.E178E; 1:1212042-1212042 |
thyroid | other; neoplasm | Substitution - coding silent |
c.631G>T; p.G211W; 1:1211945-1211945 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.760C>T; p.P254S; 1:1211707-1211707 |
skin | malignant_melanoma | Substitution - Missense |
c.518C>G; p.A173G; 1:1212058-1212058 |
lung; right_lower_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.545C>T; p.P182L; 1:1212031-1212031 |
skin | malignant_melanoma | Substitution - Missense |
c.804C>T; p.A268A; 1:1211585-1211585 |
pancreas | carcinoma | Substitution - coding silent |
c.643G>A; p.V215I; 1:1211824-1211824 |
skin | malignant_melanoma | Substitution - Missense |
c.726_727GG>AA; p.D243N; 1:1211740-1211741 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.177C>A; p.S59S; 1:1213754-1213754 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.275G>T; p.G92V; 1:1213087-1213087 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.299C>T; p.T100M; 1:1213063-1213063 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.346C>A; p.L116M; 1:1213016-1213016 |
prostate | carcinoma; adenocarcinoma | Substitution - Missense |
c.819C>T; p.T273T; 1:1211570-1211570 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.390A>G; p.P130P; 1:1212685-1212685 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.80C>T; p.T27M; 1:1214048-1214048 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.496T>C; p.C166R; 1:1212080-1212080 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.593C>A; p.T198N; 1:1211983-1211983 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.133G>A; p.E45K; 1:1213995-1213995 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.381C>T; p.P127P; 1:1212694-1212694 |
skin | malignant_melanoma | Substitution - coding silent |
c.551_552CC>TT; p.A184V; 1:1212024-1212025 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.380C>T; p.P127L; 1:1212695-1212695 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.316G>C; p.V106L; 1:1213046-1213046 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.790C>T; p.Q264*; 1:1211599-1211599 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Nonsense |