| General information | Literature | Expression | Regulation | Mutation | Homolog | Interaction |
Basic Information | |
|---|---|
Gene ID | 59277 |
Name | NTN4 |
Synonymous | netrin 4;NTN4;netrin 4 |
Definition | beta-netrin|hepar-derived netrin-like protein|netrin-4 |
Position | 12q22 |
Gene Type | protein-coding |
COSMIC somatic mutation [Top] | |||
Mutation (CDS; AA; Chr) | Site | Histology | Mutation Type |
|---|---|---|---|
c.823C>T; p.H275Y; 12:95737907-95737907 |
prostate | adenoma | Substitution - Missense |
c.823C>T; p.H275Y; 12:95737907-95737907 |
skin | malignant_melanoma | Substitution - Missense |
c.1678T>A; p.F560I; 12:95665882-95665882 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1394+1G>A; p.?; 12:95683497-95683497 |
skin; face | carcinoma; squamous_cell_carcinoma | Unknown |
c.464A>C; p.K155T; 12:95787060-95787060 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1671G>A; p.L557L; 12:95665889-95665889 |
skin | malignant_melanoma | Substitution - coding silent |
c.134G>A; p.R45Q; 12:95787390-95787390 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1216C>T; p.P406S; 12:95683676-95683676 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1649A>T; p.K550M; 12:95665911-95665911 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1103G>A; p.G368E; 12:95710518-95710518 |
skin | malignant_melanoma | Substitution - Missense |
c.435C>A; p.D145E; 12:95787089-95787089 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; acute_myeloid_leukaemia | Substitution - Missense |
c.1029C>T; p.F343F; 12:95710592-95710592 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1029C>T; p.F343F; 12:95710592-95710592 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - coding silent |
c.938A>T; p.D313V; 12:95713265-95713265 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.175G>A; p.E59K; 12:95787349-95787349 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.175G>A; p.E59K; 12:95787349-95787349 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.175G>A; p.E59K; 12:95787349-95787349 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.987C>T; p.C329C; 12:95713216-95713216 |
prostate | carcinoma | Substitution - coding silent |
c.209T>A; p.L70Q; 12:95787315-95787315 |
oesophagus | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1780G>A; p.D594N; 12:95659193-95659193 |
NS | malignant_melanoma | Substitution - Missense |
c.323C>G; p.S108C; 12:95787201-95787201 |
haematopoietic_and_lymphoid_tissue | haematopoietic_neoplasm; myelofibrosis | Substitution - Missense |
c.900A>C; p.A300A; 12:95713303-95713303 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.900A>C; p.A300A; 12:95713303-95713303 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.217C>T; p.R73W; 12:95787307-95787307 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.217C>T; p.R73W; 12:95787307-95787307 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.806A>C; p.D269A; 12:95737924-95737924 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; Burkitt_lymphoma | Substitution - Missense |
c.914A>G; p.Q305R; 12:95713289-95713289 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1285C>T; p.R429*; 12:95683607-95683607 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.1210G>A; p.V404I; 12:95683682-95683682 |
upper_aerodigestive_tract; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1202G>A; p.G401E; 12:95683690-95683690 |
skin | malignant_melanoma | Substitution - Missense |
c.1084T>A; p.C362S; 12:95710537-95710537 |
kidney | carcinoma; clear_cell_renal_cell_carcinoma | Substitution - Missense |
c.326C>T; p.A109V; 12:95787198-95787198 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.613T>C; p.Y205H; 12:95738117-95738117 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.787T>A; p.F263I; 12:95737943-95737943 |
skin | malignant_melanoma | Substitution - Missense |
c.1122C>T; p.C374C; 12:95710499-95710499 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.568C>T; p.P190S; 12:95786956-95786956 |
skin | malignant_melanoma | Substitution - Missense |
c.568C>T; p.P190S; 12:95786956-95786956 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1681C>T; p.R561*; 12:95665879-95665879 |
skin | malignant_melanoma | Substitution - Nonsense |
c.265C>T; p.H89Y; 12:95787259-95787259 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.265C>T; p.H89Y; 12:95787259-95787259 |
upper_aerodigestive_tract; mouth | carcinoma | Substitution - Missense |
c.265C>T; p.H89Y; 12:95787259-95787259 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1441G>A; p.V481M; 12:95682776-95682776 |
prostate | carcinoma | Substitution - Missense |
c.1138C>T; p.R380C; 12:95710483-95710483 |
skin | malignant_melanoma | Substitution - Missense |
c.1138C>T; p.R380C; 12:95710483-95710483 |
skin | malignant_melanoma | Substitution - Missense |
c.1628A>G; p.E543G; 12:95665932-95665932 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1652T>C; p.V551A; 12:95665908-95665908 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1236C>T; p.F412F; 12:95683656-95683656 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1236C>T; p.F412F; 12:95683656-95683656 |
urinary_tract; bladder | carcinoma; transitional_cell_carcinoma | Substitution - coding silent |
c.91G>A; p.E31K; 12:95787433-95787433 |
skin | malignant_melanoma | Substitution - Missense |
c.1012G>A; p.A338T; 12:95710609-95710609 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1516T>C; p.C506R; 12:95670141-95670141 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1425T>C; p.V475V; 12:95682792-95682792 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1753T>G; p.L585V; 12:95659220-95659220 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.676G>T; p.V226L; 12:95738054-95738054 |
liver | carcinoma | Substitution - Missense |
c.1518C>T; p.C506C; 12:95670139-95670139 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1181C>T; p.P394L; 12:95683711-95683711 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1181C>T; p.P394L; 12:95683711-95683711 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1181C>T; p.P394L; 12:95683711-95683711 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1473G>A; p.W491*; 12:95682744-95682744 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1473G>A; p.W491*; 12:95682744-95682744 |
skin | malignant_melanoma | Substitution - Nonsense |
c.1060C>T; p.R354C; 12:95710561-95710561 |
skin | malignant_melanoma | Substitution - Missense |
c.802G>C; p.A268P; 12:95737928-95737928 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1276delG; p.V426fs*44; 12:95683616-95683616 |
large_intestine | carcinoma; adenocarcinoma | Deletion - Frameshift |
c.981C>T; p.N327N; 12:95713222-95713222 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - coding silent |
c.1141G>A; p.D381N; 12:95710480-95710480 |
ovary | carcinoma; serous_carcinoma | Substitution - Missense |
c.490T>C; p.C164R; 12:95787034-95787034 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.203C>T; p.T68M; 12:95787321-95787321 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.203C>T; p.T68M; 12:95787321-95787321 |
central_nervous_system; brain | glioma | Substitution - Missense |
c.361C>T; p.L121L; 12:95787163-95787163 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.982G>A; p.E328K; 12:95713221-95713221 |
skin | malignant_melanoma | Substitution - Missense |
c.982G>A; p.E328K; 12:95713221-95713221 |
skin | malignant_melanoma | Substitution - Missense |
c.982G>A; p.E328K; 12:95713221-95713221 |
skin | malignant_melanoma | Substitution - Missense |
c.982G>A; p.E328K; 12:95713221-95713221 |
skin | malignant_melanoma | Substitution - Missense |
c.1168G>T; p.D390Y; 12:95710453-95710453 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.133C>T; p.R45*; 12:95787391-95787391 |
lung | carcinoma; small_cell_carcinoma | Substitution - Nonsense |
c.768C>T; p.F256F; 12:95737962-95737962 |
skin | malignant_melanoma | Substitution - coding silent |
c.1883A>G; p.K628R; 12:95659090-95659090 |
skin | malignant_melanoma | Substitution - Missense |
c.703C>G; p.P235A; 12:95738027-95738027 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.381C>A; p.F127L; 12:95787143-95787143 |
NS | NS | Substitution - Missense |
c.940C>T; p.R314W; 12:95713263-95713263 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1182G>A; p.P394P; 12:95683710-95683710 |
breast | carcinoma | Substitution - coding silent |
c.1369C>A; p.P457T; 12:95683523-95683523 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1369C>A; p.P457T; 12:95683523-95683523 |
upper_aerodigestive_tract; mouth | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1379G>A; p.G460E; 12:95683513-95683513 |
oesophagus; middle_third | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.275C>T; p.S92F; 12:95787249-95787249 |
breast | carcinoma | Substitution - Missense |
c.364G>A; p.E122K; 12:95787160-95787160 |
skin | malignant_melanoma | Substitution - Missense |
c.1134C>G; p.F378L; 12:95710487-95710487 |
urinary_tract; bladder | carcinoma | Substitution - Missense |
c.1680C>T; p.F560F; 12:95665880-95665880 |
skin | malignant_melanoma | Substitution - coding silent |
c.328G>A; p.E110K; 12:95787196-95787196 |
skin | malignant_melanoma | Substitution - Missense |
c.1712G>A; p.W571*; 12:95665848-95665848 |
skin | malignant_melanoma | Substitution - Nonsense |
c.20T>G; p.L7R; 12:95790290-95790290 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1007G>C; p.G336A; 12:95710614-95710614 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1308G>A; p.V436V; 12:95683584-95683584 |
urinary_tract; bladder | carcinoma | Substitution - coding silent |
c.1030G>A; p.D344N; 12:95710591-95710591 |
skin | malignant_melanoma | Substitution - Missense |
c.1777G>A; p.E593K; 12:95659196-95659196 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1777G>A; p.E593K; 12:95659196-95659196 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.1301G>C; p.C434S; 12:95683591-95683591 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.1838C>A; p.P613H; 12:95659135-95659135 |
large_intestine; caecum | carcinoma; adenocarcinoma | Substitution - Missense |
c.1148G>A; p.R383Q; 12:95710473-95710473 |
skin | malignant_melanoma | Substitution - Missense |
c.1148G>A; p.R383Q; 12:95710473-95710473 |
skin | malignant_melanoma | Substitution - Missense |
c.658A>G; p.K220E; 12:95738072-95738072 |
skin; trunk | malignant_melanoma | Substitution - Missense |
c.338A>C; p.H113P; 12:95787186-95787186 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.109C>T; p.R37W; 12:95787415-95787415 |
stomach | carcinoma; adenocarcinoma | Substitution - Missense |
c.114G>A; p.M38I; 12:95787410-95787410 |
skin | malignant_melanoma | Substitution - Missense |
c.1456G>A; p.E486K; 12:95682761-95682761 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.408C>T; p.S136S; 12:95787116-95787116 |
skin | malignant_melanoma | Substitution - coding silent |
c.1325G>A; p.G442E; 12:95683567-95683567 |
skin | malignant_melanoma | Substitution - Missense |
c.999G>T; p.K333N; 12:95710622-95710622 |
liver | carcinoma; hepatocellular_carcinoma | Substitution - Missense |
c.999G>T; p.K333N; 12:95710622-95710622 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.1355C>T; p.A452V; 12:95683537-95683537 |
pancreas | carcinoma | Substitution - Missense |
c.1355C>T; p.A452V; 12:95683537-95683537 |
pancreas | carcinoma | Substitution - Missense |
c.622G>A; p.E208K; 12:95738108-95738108 |
skin | malignant_melanoma | Substitution - Missense |
c.1149G>A; p.R383R; 12:95710472-95710472 |
skin | malignant_melanoma | Substitution - coding silent |
c.506G>A; p.G169D; 12:95787018-95787018 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1165C>T; p.P389S; 12:95710456-95710456 |
skin | malignant_melanoma | Substitution - Missense |
c.375C>A; p.F125L; 12:95787149-95787149 |
endometrium | carcinoma; endometrioid_carcinoma | Substitution - Missense |
c.2T>C; p.M1T; 12:95790308-95790308 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1418A>C; p.H473P; 12:95682799-95682799 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.733C>A; p.P245T; 12:95737997-95737997 |
large_intestine | carcinoma; adenocarcinoma | Substitution - Missense |
c.1418A>C; p.H473P; 12:95682799-95682799 |
central_nervous_system; brain | glioma; astrocytoma_Grade_IV | Substitution - Missense |
c.417G>T; p.P139P; 12:95787107-95787107 |
lung | carcinoma; squamous_cell_carcinoma | Substitution - coding silent |
c.1220C>T; p.A407V; 12:95683672-95683672 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.333T>G; p.D111E; 12:95787191-95787191 |
thyroid | carcinoma | Substitution - Missense |
c.1723G>A; p.G575R; 12:95665837-95665837 |
haematopoietic_and_lymphoid_tissue | lymphoid_neoplasm; chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma | Substitution - Missense |
c.1843C>T; p.L615F; 12:95659130-95659130 |
large_intestine; rectum | carcinoma; adenocarcinoma | Substitution - Missense |
c.304C>T; p.P102S; 12:95787220-95787220 |
skin | malignant_melanoma | Substitution - Missense |
c.949G>A; p.E317K; 12:95713254-95713254 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.949G>A; p.E317K; 12:95713254-95713254 |
skin; head_neck | carcinoma; squamous_cell_carcinoma | Substitution - Missense |
c.1600T>C; p.S534P; 12:95665960-95665960 |
lung | carcinoma; adenocarcinoma | Substitution - Missense |
c.1515A>G; p.K505K; 12:95670142-95670142 |
breast | carcinoma | Substitution - coding silent |
c.615C>A; p.Y205*; 12:95738115-95738115 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Nonsense |
c.95A>G; p.K32R; 12:95787429-95787429 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1356G>A; p.A452A; 12:95683536-95683536 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - coding silent |
c.535G>A; p.A179T; 12:95786989-95786989 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |
c.1838C>G; p.P613R; 12:95659135-95659135 |
oesophagus | carcinoma; adenocarcinoma | Substitution - Missense |
c.1172C>G; p.A391G; 12:95710449-95710449 |
pancreas | carcinoma; acinar_carcinoma | Substitution - Missense |
c.751T>C; p.Y251H; 12:95737979-95737979 |
lung; right_upper_lobe | carcinoma; adenocarcinoma | Substitution - Missense |
c.1142A>G; p.D381G; 12:95710479-95710479 |
large_intestine; colon | carcinoma; adenocarcinoma | Substitution - Missense |