EuRBPDB

Note: to get the extension of tumor abbreviations.

Cancer Related Information
Basic Information

Differential Expression

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq
ACC	chr5	37328403	Missense_Mutation	novel	G611S	0.03
BLCA	chr5	37324062	Missense_Mutation	NA	E713Q	0.5
BLCA	chr5	37328394	Missense_Mutation	novel	Y614N	0.3
BLCA	chr5	37291979	Missense_Mutation	rs140076285	S1366C	0.27
BLCA	chr5	37329237	Missense_Mutation	rs375786815	P589L	0.51
BLCA	chr5	37358120	Missense_Mutation	NA	E142K	0.18
BLCA	chr5	37292926	Silent	NA	L1330L	0.32
BLCA	chr5	37371086	5'UTR	novel		0.27
BLCA	chr5	37370928	Missense_Mutation	NA	A17V	0.16
BLCA	chr5	37371038	5'UTR	NA		0.24
BLCA	chr5	37370951	Silent	NA	A9A	0.18
BLCA	chr5	37350199	Missense_Mutation	novel	L264I	0.15
BLCA	chr5	37291914	Missense_Mutation	novel	E1388Q	0.05
BLCA	chr5	37325911	Missense_Mutation	novel	E694V	0.54
BLCA	chr5	37325912	Missense_Mutation	novel	E694Q	0.54
BLCA	chr5	37294429	Missense_Mutation	novel	T1277S	0.09
BLCA	chr5	37350176	Silent	novel	F271F	0.17
BLCA	chr5	37329241	Missense_Mutation	novel	L588V	0.34
BLCA	chr5	37325914	Missense_Mutation	novel	R693I	0.12
BLCA	chr5	37318032	Missense_Mutation	novel	G754E	0.06
BLCA	chr5	37351232	Missense_Mutation	novel	F227L	0.39
BLCA	chr5	37370956	Missense_Mutation	NA	A8T	0.12
BLCA	chr5	37331708	Missense_Mutation	novel	E536K	0.3
BLCA	chr5	37363931	Missense_Mutation	novel	L117I	0.15
BRCA	chr5	37371041	5'UTR	novel		0.11
BRCA	chr5	37309145	Nonsense_Mutation	novel	C917*	0.08
BRCA	chr5	37310552	Missense_Mutation	NA	K876N	0.31
BRCA	chr5	37333593	Missense_Mutation	rs751958347	A463V	0.31
BRCA	chr5	37314312	Missense_Mutation	NA	E774D	0.28
BRCA	chr5	37370951	Silent	NA	A9A	0.3
BRCA	chr5	37298936	Missense_Mutation	novel	H1242R	0.24
BRCA	chr5	37327635	Missense_Mutation	NA	I673N	0.16
BRCA	chr5	37348559	Missense_Mutation	novel	R314T	0.1
BRCA	chr5	37358117	Missense_Mutation	NA	T143P	0.3
BRCA	chr5	37310629	Missense_Mutation	rs749163402	A851T	0.27
BRCA	chr5	37303356	Missense_Mutation	NA	R1074T	0.25
BRCA	chr5	37341209	Missense_Mutation	novel	R376T	0.32
BRCA	chr5	37370888	Silent	NA	I30I	0.15
BRCA	chr5	37330051	Silent	NA	R571R	0.29
CESC	chr5	37298883	Missense_Mutation	rs764447032	R1260C	0.1
CESC	chr5	37370940	Missense_Mutation	novel	S13C	0.3
CESC	chr5	37305173	Missense_Mutation	novel	E981K	0.11
CESC	chr5	37310686	Missense_Mutation	NA	E832Q	0.35
CESC	chr5	37331754	Silent	NA	L520L	0.77
CESC	chr5	37341119	Nonsense_Mutation	NA	S406*	0.44
CESC	chr5	37299505	Missense_Mutation	novel	A1209T	0.32
CESC	chr5	37364299	Missense_Mutation	NA	I81M	0.39
CESC	chr5	37341236	Missense_Mutation	novel	R367M	0.19
CESC	chr5	37333580	Missense_Mutation	novel	L467F	0.45
CESC	chr5	37327720	Missense_Mutation	novel	Q645E	0.45
CESC	chr5	37341239	Missense_Mutation	NA	V366A	0.5
CESC	chr5	37302793	Missense_Mutation	NA	E1145Q	0.17
CESC	chr5	37307402	Missense_Mutation	rs766476048	S933C	0.21
COAD	chr5	37294331	Missense_Mutation	NA	R1310W	0.15
COAD	chr5	37307431	Splice_Region	NA	V923V	0.3
COAD	chr5	37305119	Missense_Mutation	NA	P999T	0.09
COAD	chr5	37325902	Missense_Mutation	novel	A697V	0.18
COAD	chr5	37351289	Silent	novel	L208L	0.34
COAD	chr5	37337880	Missense_Mutation	NA	D429Y	0.29
COAD	chr5	37333551	Frame_Shift_Del	NA	*N477Tfs7**	0.25
COAD	chr5	37350157	Splice_Region	novel		0.26
COAD	chr5	37348536	Missense_Mutation	novel	A322T	0.33
COAD	chr5	37352772	Missense_Mutation	NA	V174A	0.27
COAD	chr5	37337864	Missense_Mutation	novel	V434A	0.05
COAD	chr5	37364270	Missense_Mutation	novel	P91H	0.06
COAD	chr5	37294327	Splice_Site	NA	X1310_splice	0.25
COAD	chr5	37333554	Nonsense_Mutation	NA	L476*	0.23
COAD	chr5	37333487	Missense_Mutation	NA	K498N	0.13
COAD	chr5	37333507	Nonsense_Mutation	novel	Q492*	0.34
COAD	chr5	37291931	Missense_Mutation	NA	S1382F	0.31
GBM	chr5	37292959	Frame_Shift_Ins	novel	*P1320Cfs13**	0.1
GBM	chr5	37352790	Missense_Mutation	rs371884662	A168V	0.28
GBM	chr5	37301503	Nonsense_Mutation	novel	Y1165*	0.04
GBM	chr5	37303258	Splice_Site	novel	X1106_splice	0.2
GBM	chr5	37310656	Missense_Mutation	novel	I842V	0.44
GBM	chr5	37370720	Intron	novel		0.24
GBM	chr5	37301475	Missense_Mutation	novel	V1175L	0.06
GBM	chr5	37309208	Missense_Mutation	novel	M896I	0.56
GBM	chr5	37329194	Silent	novel	Y603Y	0.27
GBM	chr5	37333583	Missense_Mutation	novel	E466D	0.16
GBM	chr5	37291895	3'UTR	novel		0.09
GBM	chr5	37292020	Silent	novel	L1352L	0.1
GBM	chr5	37302805	Missense_Mutation	novel	L1141I	0.42
HNSC	chr5	37331731	Frame_Shift_Del	novel	*V528Gfs55**	0.25
HNSC	chr5	37307311	Missense_Mutation	novel	Q963H	0.15
HNSC	chr5	37331793	Splice_Region	novel	G507G	0.08
HNSC	chr5	37363937	Missense_Mutation	novel	A115P	0.04
HNSC	chr5	37329276	Missense_Mutation	rs748082598	Y576C	0.28
HNSC	chr5	37371000	5'UTR	novel		0.08
HNSC	chr5	37291850	3'UTR	novel		0.06
HNSC	chr5	37348504	Splice_Site	novel	X332_splice	0.08
HNSC	chr5	37303381	Nonsense_Mutation	NA	R1066*	0.23
HNSC	chr5	37302828	Nonsense_Mutation	novel	S1133*	0.19
HNSC	chr5	37363893	Silent	novel	E129E	0.45
HNSC	chr5	37327721	Silent	novel	T644T	0.1
KIRC	chr5	37318023	Missense_Mutation	novel	Q757L	0.04
KIRP	chr5	37307307	Missense_Mutation	rs780165777	F965L	0.39
LAML	chr5	37298870	Nonsense_Mutation	novel	L1264*	0.16
LAML	chr5	37309171	Missense_Mutation	novel	N909H	0.14
LAML	chr5	37325905	Missense_Mutation	novel	T696I	0.14
LGG	chr5	37309221	Missense_Mutation	NA	E892G	0.27
LGG	chr5	37351222	Missense_Mutation	NA	K231E	0.15
LGG	chr5	37292964	Missense_Mutation	novel	K1318Q	0.1
LGG	chr5	37294407	Silent	rs768396938	F1284F	0.42
LGG	chr5	37324103	Missense_Mutation	novel	E699A	0.1
LGG	chr5	37350242	Silent	novel	Q249Q	0.05
LGG	chr5	37363975	Missense_Mutation	NA	C102S	0.46
LIHC	chr5	37352798	Silent	novel	L165L	0.18
LIHC	chr5	37302881	Silent	novel	L1115L	0.44
LIHC	chr5	37291907	Missense_Mutation	novel	L1390R	0.14
LIHC	chr5	37341087	Splice_Region	novel		0.64
LIHC	chr5	37370880	Missense_Mutation	novel	Q33R	0.13
LIHC	chr5	37351305	Missense_Mutation	NA	D203G	0.32
LUAD	chr5	37328355	Splice_Region	novel		0.56
LUAD	chr5	37303321	Missense_Mutation	rs774103498	E1086K	0.09
LUAD	chr5	37291969	Silent	rs189615754	S1369S	0.24
LUAD	chr5	37342639	Missense_Mutation	novel	D335Y	0.43
LUAD	chr5	37305071	Nonsense_Mutation	novel	E1015*	0.08
LUAD	chr5	37341107	Missense_Mutation	NA	R410I	0.21
LUAD	chr5	37348540	Missense_Mutation	novel	Q320H	0.07
LUAD	chr5	37370894	Silent	NA	R28R	0.19
LUAD	chr5	37370891	Silent	rs772659342	L29L	0.23
LUAD	chr5	37370733	Intron	novel		0.49
LUAD	chr5	37299541	Missense_Mutation	novel	K1197E	0.17
LUAD	chr5	37331714	Missense_Mutation	novel	E534Q	0.07
LUAD	chr5	37310622	Missense_Mutation	novel	D853V	0.06
LUAD	chr5	37364285	Missense_Mutation	novel	R86K	0.13
LUAD	chr5	37363970	In_Frame_Ins	novel	N103dup	0.37
LUSC	chr5	37299467	Nonsense_Mutation	NA	W1221*	0.38
LUSC	chr5	37294428	Silent	novel	T1277T	0.13
LUSC	chr5	37352785	Missense_Mutation	rs771577745	P170S	0.11
LUSC	chr5	37328380	Silent	rs73749020	S618S	0.33
LUSC	chr5	37358094	Silent	novel	V150V	0.16
LUSC	chr5	37305095	Missense_Mutation	NA	D1007N	0.23
LUSC	chr5	37352815	Missense_Mutation	novel	H160Y	0.42
LUSC	chr5	37298931	Missense_Mutation	novel	L1244V	0.26
LUSC	chr5	37371090	5'UTR	novel		0.06
LUSC	chr5	37348554	Missense_Mutation	NA	A316S	0.14
LUSC	chr5	37303356	Missense_Mutation	NA	R1074T	0.07
LUSC	chr5	37292923	Silent	NA	L1331L	0.22
LUSC	chr5	37307390	Missense_Mutation	NA	A937V	0.33
LUSC	chr5	37350173	Silent	NA	T272T	0.44
LUSC	chr5	37358096	Missense_Mutation	novel	V150M	0.15
LUSC	chr5	37363986	Splice_Site	novel	X99_splice	0.79
LUSC	chr5	37370865	Missense_Mutation	novel	R38P	0.14
LUSC	chr5	37292969	Missense_Mutation	NA	R1316T	0.29
LUSC	chr5	37350200	Silent	NA	F263F	0.12
LUSC	chr5	37309177	Missense_Mutation	novel	I907V	0.07
LUSC	chr5	37310698	Missense_Mutation	novel	I828L	0.61
LUSC	chr5	37303332	Missense_Mutation	novel	W1082L	0.31
LUSC	chr5	37350185	Missense_Mutation	novel	L268F	0.27
MESO	chr5	37303327	Missense_Mutation	novel	Y1084D	0.06
MESO	chr5	37299488	Silent	novel	P1214P	0.58
OV	chr5	37318009	Nonsense_Mutation	NA	E762*	0.22
OV	chr5	37302890	Silent	novel	Q1112Q	0.07
OV	chr5	37291877	3'UTR	novel		0.05
OV	chr5	37327715	Silent	NA	A646A	0.17
OV	chr5	37299560	Silent	NA	G1190G	0.35
OV	chr5	37292977	Frame_Shift_Del	novel	*W1314Gfs4**	0.1
OV	chr5	37301542	Missense_Mutation	novel	R1152S	0.12
OV	chr5	37348576	Missense_Mutation	novel	D308E	0.04
OV	chr5	37330073	Silent	NA	R563R	0.46
OV	chr5	37302859	Missense_Mutation	NA	L1123V	0.15
OV	chr5	37310669	Missense_Mutation	rs780853280	L837F	0.16
OV	chr5	37307422	Nonsense_Mutation	NA	Y926*	0.19
OV	chr5	37325954	Missense_Mutation	novel	A680P	0.24
PAAD	chr5	37370875	Missense_Mutation	novel	Q35E	0.03
PAAD	chr5	37324053	Missense_Mutation	novel	G716S	0.15
PAAD	chr5	37331724	Silent	novel	G530G	0.21
PAAD	chr5	37370705	Intron	novel		0.19
READ	chr5	37304750	Missense_Mutation	NA	K1051Q	0.15
READ	chr5	37307376	Missense_Mutation	NA	P942S	0.27
READ	chr5	37358085	Silent	novel	K153K	0.07
READ	chr5	37307395	Silent	NA	T935T	0.27
READ	chr5	37299538	Missense_Mutation	novel	L1198F	0.13
READ	chr5	37299548	Missense_Mutation	novel	D1194E	0.15
READ	chr5	37318017	Missense_Mutation	novel	M759T	0.38
SARC	chr5	37348584	Missense_Mutation	novel	G306R	0.38
SKCM	chr5	37292974	Missense_Mutation	novel	W1314C	0.31
SKCM	chr5	37350179	Silent	NA	Q270Q	0.56
SKCM	chr5	37364379	Missense_Mutation	novel	P55S	0.45
SKCM	chr5	37328380	Silent	NA	S618S	0.45
SKCM	chr5	37341234	Silent	NA	L368L	0.58
SKCM	chr5	37364375	Missense_Mutation	NA	T56I	0.09
SKCM	chr5	37298910	Missense_Mutation	rs764584056	L1251F	0.27
SKCM	chr5	37309244	Silent	novel	S884S	0.61
SKCM	chr5	37309183	Nonsense_Mutation	NA	Q905*	0.16
SKCM	chr5	37337847	Missense_Mutation	NA	P440S	0.33
SKCM	chr5	37363936	Missense_Mutation	novel	A115V	0.09
SKCM	chr5	37364275	Silent	novel	L89L	0.22
SKCM	chr5	37342640	Silent	rs769531630	I334I	0.18
SKCM	chr5	37302805	Missense_Mutation	novel	L1141F	0.15
SKCM	chr5	37299532	Missense_Mutation	NA	E1200K	0.39
SKCM	chr5	37309172	Silent	NA	S908S	0.16
SKCM	chr5	37309174	Missense_Mutation	NA	S908C	0.17
SKCM	chr5	37337847	Missense_Mutation	NA	P440S	0.41
SKCM	chr5	37342625	Silent	NA	F339F	0.18
SKCM	chr5	37337847	Missense_Mutation	NA	P440S	0.2
SKCM	chr5	37294407	Silent	rs768396938	F1284F	0.33
STAD	chr5	37333592	Silent	rs142662644	A463A	0.08
STAD	chr5	37329255	Missense_Mutation	novel	R583I	0.23
STAD	chr5	37341206	Missense_Mutation	novel	Q377R	0.17
STAD	chr5	37350234	Missense_Mutation	NA	R252K	0.04
STAD	chr5	37294435	Missense_Mutation	novel	V1275A	0.08
STAD	chr5	37309164	Missense_Mutation	NA	V911A	0.37
STAD	chr5	37298961	Missense_Mutation	NA	T1234A	0.36
STAD	chr5	37364284	Silent	NA	R86R	0.1
STAD	chr5	37301482	Missense_Mutation	novel	Q1172H	0.09
STAD	chr5	37371052	5'UTR	novel		0.5
STAD	chr5	37314288	Silent	NA	Q782Q	0.25
STAD	chr5	37352809	Nonsense_Mutation	rs765177729	R162*	0.13
STAD	chr5	37291969	Silent	rs189615754	S1369S	0.28
STAD	chr5	37342564	Missense_Mutation	novel	A360S	0.12
STAD	chr5	37309177	Frame_Shift_Del	NA	*I907Lfs17**	0.15
STAD	chr5	37292896	Missense_Mutation	NA	Q1340H	0.17
STAD	chr5	37294414	Missense_Mutation	NA	V1282A	0.1
STAD	chr5	37314325	Missense_Mutation	NA	A770D	0.15
STAD	chr5	37342576	Missense_Mutation	novel	C356S	0.4
STAD	chr5	37299556	Missense_Mutation	NA	F1192I	0.46
THCA	chr5	37299503	Silent	rs149980171	A1209A	0.05
THCA	chr5	37314313	Nonsense_Mutation	novel	*E774Gfs7**	0.11
UCEC	chr5	37291908	Missense_Mutation	novel	L1390F	0.08
UCEC	chr5	37303351	Missense_Mutation	rs376467373	R1076C	0.14
UCEC	chr5	37303330	Missense_Mutation	rs767440970	R1083W	0.44
UCEC	chr5	37333624	Missense_Mutation	novel	G453S	0.48
UCEC	chr5	37294407	Silent	rs768396938	F1284F	0.38
UCEC	chr5	37302867	Missense_Mutation	rs373119361	R1120Q	0.41
UCEC	chr5	37304815	Missense_Mutation	rs776784941	R1029Q	0.47
UCEC	chr5	37309267	Missense_Mutation	novel	A877T	0.38
UCEC	chr5	37298928	Missense_Mutation	novel	S1245G	0.34
UCEC	chr5	37309128	Splice_Site	novel	X923_splice	0.37
UCEC	chr5	37310714	Silent	NA	T822T	0.15
UCEC	chr5	37303381	Nonsense_Mutation	NA	R1066*	0.11
UCEC	chr5	37314234	Silent	rs747162889	E800E	0.35
UCEC	chr5	37299496	Missense_Mutation	novel	S1212P	0.15
UCEC	chr5	37303351	Missense_Mutation	rs376467373	R1076C	0.32
UCEC	chr5	37314258	Silent	novel	L792L	0.06
UCEC	chr5	37324062	Nonsense_Mutation	novel	E713*	0.37
UCEC	chr5	37307366	Missense_Mutation	novel	L945P	0.25
UCEC	chr5	37337859	Missense_Mutation	novel	H436Y	0.19
UCEC	chr5	37341179	Missense_Mutation	rs368991435	T386M	0.29
UCEC	chr5	37291905	Missense_Mutation	novel	H1391N	0.39
UCEC	chr5	37302790	Nonsense_Mutation	novel	E1146*	0.16
UCEC	chr5	37307393	Missense_Mutation	NA	A936V	0.23
UCEC	chr5	37301509	Silent	rs767130555	R1163R	0.4
UCEC	chr5	37309160	Silent	novel	D912D	0.47
UCEC	chr5	37307353	Missense_Mutation	novel	F949L	0.46
UCEC	chr5	37318017	Missense_Mutation	novel	M759K	0.48
UCEC	chr5	37341196	Silent	novel	A380A	0.27
UCEC	chr5	37291970	Missense_Mutation	novel	S1369L	0.36
UCEC	chr5	37307353	Missense_Mutation	novel	F949L	0.38
UCEC	chr5	37318045	Missense_Mutation	rs780373258	R750C	0.4
UCEC	chr5	37302817	Missense_Mutation	rs758413180	D1137N	0.27
UCEC	chr5	37364337	Nonsense_Mutation	novel	G69*	0.24
UCEC	chr5	37331700	Missense_Mutation	novel	F538L	0.12
UCEC	chr5	37351203	Missense_Mutation	novel	E237G	0.28
UCEC	chr5	37363947	Silent	rs754151251	P111P	0.44
UCEC	chr5	37370870	Missense_Mutation	novel	E36D	0.28
UCEC	chr5	37292022	Missense_Mutation	novel	L1352I	0.45
UCEC	chr5	37292930	Missense_Mutation	novel	V1329A	0.38
UCEC	chr5	37298882	Missense_Mutation	rs142078226	R1260H	0.37
UCEC	chr5	37351356	Missense_Mutation	rs759024955	G186D	0.46
UCEC	chr5	37364304	Nonsense_Mutation	novel	E80*	0.53
UCEC	chr5	37301453	Missense_Mutation	novel	L1182P	0.09
UCEC	chr5	37303351	Missense_Mutation	rs376467373	R1076C	0.13
UCEC	chr5	37342635	Missense_Mutation	rs376696300	R336H	0.26
UCEC	chr5	37324060	Missense_Mutation	novel	E713D	0.29
UCEC	chr5	37298937	Missense_Mutation	novel	H1242Y	0.09
UCEC	chr5	37370755	Intron	novel		0.28
UCEC	chr5	37333593	Missense_Mutation	rs751958347	A463V	0.46
UCEC	chr5	37330116	Missense_Mutation	novel	A549V	0.51
UCEC	chr5	37333629	Missense_Mutation	novel	T451I	0.31
UCEC	chr5	37364256	Nonsense_Mutation	novel	Q96*	0.36
UCEC	chr5	37370683	Intron	novel		0.58
UCEC	chr5	37314271	Missense_Mutation	novel	S788L	0.05
UCEC	chr5	37302900	Missense_Mutation	NA	I1109S	0.3
UCEC	chr5	37301489	Missense_Mutation	novel	S1170F	0.49
UCEC	chr5	37310629	Missense_Mutation	rs749163402	A851T	0.34
UCEC	chr5	37327750	Missense_Mutation	novel	P635T	0.22
UCEC	chr5	37370773	Intron	novel		0.22
UCEC	chr5	37305149	Missense_Mutation	NA	A989T	0.33
UCEC	chr5	37307400	Missense_Mutation	novel	L934I	0.45
UCEC	chr5	37370680	Intron	novel		0.5
UCEC	chr5	37342590	Missense_Mutation	novel	S351Y	0.41
UCEC	chr5	37364373	Missense_Mutation	rs144607433	V57I	0.26
UCS	chr5	37291874	3'UTR	novel		0.29

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
COAD	AMP	0.1663	0.030224
LUAD	AMP	0.5291	6.849e-09
LUSC	AMP	0.6766	3.0539e-09
TGCT	DEL	0.5867	0.11998
THCA	DEL	0	0.23456

Survival Analysis

Cancer	P-value	Q-value
THYM	0.0071	Kaplan-Meier Survival Analysis
KIRC	0.0071	Kaplan-Meier Survival Analysis
SARC	0.032	Kaplan-Meier Survival Analysis
MESO	0.00039	Kaplan-Meier Survival Analysis
ACC	0.016	Kaplan-Meier Survival Analysis
BRCA	0.0085	Kaplan-Meier Survival Analysis
KIRP	0.002	Kaplan-Meier Survival Analysis
PAAD	0.05	Kaplan-Meier Survival Analysis
READ	0.022	Kaplan-Meier Survival Analysis
KICH	0.0046	Kaplan-Meier Survival Analysis
UCEC	0.0073	Kaplan-Meier Survival Analysis
LIHC	0.0001	Kaplan-Meier Survival Analysis
LGG	0.023	Kaplan-Meier Survival Analysis

Drugs

Cell lines and drugs in GSE70138 or GSE92742

Description

RBPome

Expression

Transcripts

Gene Model

Pathways

PPI

Orthologs

Gene Ontology

Description

Ensembl ID: ENSG00000113569 (Gene tree)
Gene ID: 9631
Gene Symbol: NUP155
Alias: KIAA0791|N155
Full Name: nucleoporin 155
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Minus strand
Length: 83,319 bases
Position: chr5:37,288,137-37,371,455
Accession: 8063
RBP type: non-canonical RBP
Summary: Nucleoporins are proteins that play an important role in the assembly and functioning of the nuclear pore complex (NPC) which regulates the movement of macromolecules across the nuclear envelope (NE). The protein encoded by this gene plays a role in the fusion of NE vesicles and formation of the double membrane NE. The protein may also be involved in cardiac physiology and may be associated with the pathogenesis of atrial fibrillation. Alternative splicing results in multiple transcript variants of this gene. A pseudogene associated with this gene is located on chromosome 6. [provided by RefSeq, May 2013]

RNA binding proteome (RBPome)

PID	Title	Method	Time	Author	Doi
30528433	The Human RNA-Binding Proteome and Its Dynamics during Translational Arrest	XRNAX & HEK293	2018 Dec 6	Trendel J	DOI: 10.1016/j.cell.2018.11.004
29431736	Capturing the interactome of newly transcribed RNA	PolyT-RICK & Hela	2018 Feb 12	Bao X	DOI: 10.1038/nmeth.4595
29431736	Capturing the interactome of newly transcribed RNA	RICK & Hela	2018 Feb 12	Bao X	DOI: 10.1038/nmeth.4595
30528433	The Human RNA-Binding Proteome and Its Dynamics during Translational Arrest	XRNAX & Hela	2018 Dec 6	Trendel J	DOI: 10.1016/j.cell.2018.11.004

Expression

Transcripts

Transcript ID	Name	Length	RefSeq ID	Protein ID	Length	RefSeq ID	UniportKB ID
ENST00000515054	NUP155-208	824	-	-	- (aa)	-	-
ENST00000513532	NUP155-207	4088	-	ENSP00000422019	1327 (aa)	-	E9PF10
ENST00000507233	NUP155-204	459	-	-	- (aa)	-	-
ENST00000502533	NUP155-203	1896	-	-	- (aa)	-	-
ENST00000381843	NUP155-202	4200	-	ENSP00000371265	1332 (aa)	-	O75694
ENST00000507675	NUP155-205	673	-	ENSP00000423484	54 (aa)	-	D6RA13
ENST00000508182	NUP155-206	702	-	-	- (aa)	-	-
ENST00000231498	NUP155-201	8143	XM_011514165	ENSP00000231498	1391 (aa)	XP_011512467	O75694

Gene Model

Click here to download ENSG00000113569's gene model file

Pathways

Pathway ID	Pathway Name	Source
hsa03013	RNA transport	KEGG

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000113569's network

* RBP PPI network refers to all genes directly bind to RBP

Orthologs identified by RBPome

Ensembl ID	Gene Symbol	Coverage	Identiy	Ortholog	Gene Symbol	Coverage	Identiy	Species
ENSG00000113569	NUP155	99	32.582	FBgn0021761	Nup154	99	32.837	Drosophila_melanogaster
ENSG00000113569	NUP155	100	95.120	ENSMUSG00000022142	Nup155	100	94.828	Mus_musculus

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0000972	transcription-dependent tethering of RNA polymerase II gene DNA at nuclear periphery	21873635.	IBA	Process
GO:0005215	transporter activity	10191094.	TAS	Function
GO:0005515	protein binding	25416956.	IPI	Function
GO:0005635	nuclear envelope	19070573.	IDA	Component
GO:0005635	nuclear envelope	-	TAS	Component
GO:0006110	regulation of glycolytic process	-	TAS	Process
GO:0006406	mRNA export from nucleus	-	TAS	Process
GO:0006409	tRNA export from nucleus	-	TAS	Process
GO:0006606	protein import into nucleus	21873635.	IBA	Process
GO:0006998	nuclear envelope organization	19070573.	IDA	Process
GO:0016020	membrane	19946888.	HDA	Component
GO:0016032	viral process	-	TAS	Process
GO:0016925	protein sumoylation	-	TAS	Process
GO:0017056	structural constituent of nuclear pore	21873635.	IBA	Function
GO:0019083	viral transcription	-	TAS	Process
GO:0031965	nuclear membrane	-	IDA	Component
GO:0036228	protein localization to nuclear inner membrane	21873635.	IBA	Process
GO:0043657	host cell	-	IEA	Component
GO:0044611	nuclear pore inner ring	21873635.	IBA	Component
GO:0060964	regulation of gene silencing by miRNA	-	TAS	Process
GO:0075733	intracellular transport of virus	-	TAS	Process
GO:0086014	atrial cardiac muscle cell action potential	-	IEA	Process
GO:1900034	regulation of cellular response to heat	-	TAS	Process

EuRBPDB

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Eesembl ID

Cell lines and drugs in GSE70138 or GSE92742

Description

RBPome

Expression

Transcripts

Gene Model

Pathways

PPI

Orthologs

Gene Ontology

Note: Click here to get the extension of tumor abbreviations.

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Input Drug :

Input Cell Line :

Eesembl ID

Cell lines and drugs in GSE70138 or GSE92742

Note: to get the extension of tumor abbreviations.