EuRBPDB

Basic Information
Cancer Related Information

Description

RBPome

Expression

Transcripts

Gene Model

Phenotypes

GWAS

PPI

Gene Ontology

Description

Ensembl ID: ENSG00000010292 (Gene tree)
Gene ID: 9918
Gene Symbol: NCAPD2
Alias: CNAP1|hCAP-D2|CAP-D2|KIAA0159
Full Name: non-SMC condensin I complex subunit D2
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Plus strand
Length: 38,611 bases
Position: chr12:6,493,356-6,531,966
Accession: 24305
RBP type: non-canonical RBP
Summary: (Non-SMC Condensin I Complex Subunit D2) is a Protein Coding gene. Diseases associated with NCAPD2 include Microcephaly 21, Primary, Autosomal Recessive and Microcephaly. Among its related pathways are Cell Cycle, Mitotic and Mitotic Prometaphase. Gene Ontology (GO) annotations related to this gene include binding and histone binding. An important paralog of this gene is NCAPD3.

RNA binding proteome (RBPome)

PID	Title	Method	Time	Author	Doi
30607034	Comprehensive identification of RNA protein interactions in any organism using orthogonal organic phase separation (OOPS)	OOPS & HEK293	2019 Jan 3	Queiroz RML	DOI: 10.1038/s41587-018-0001-2
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
30607034	Comprehensive identification of RNA protein interactions in any organism using orthogonal organic phase separation (OOPS)	OOPS & MCF10A	2019 Jan 3	Queiroz RML	DOI: 10.1038/s41587-018-0001-2
30607034	Comprehensive identification of RNA protein interactions in any organism using orthogonal organic phase separation (OOPS)	OOPS & U2OS	2019 Jan 3	Queiroz RML	DOI: 10.1038/s41587-018-0001-2

Expression

Transcripts

Transcript ID	Name	Length	RefSeq ID	Protein ID	Length	RefSeq ID	UniportKB ID
ENST00000536090	NCAPD2-204	654	-	-	- (aa)	-	-
ENST00000542492	NCAPD2-212	1052	-	-	- (aa)	-	-
ENST00000382457	NCAPD2-202	2844	-	ENSP00000371895	919 (aa)	-	E7EN77
ENST00000536538	NCAPD2-205	765	-	-	- (aa)	-	-
ENST00000542472	NCAPD2-211	444	-	-	- (aa)	-	-
ENST00000539885	NCAPD2-209	558	-	-	- (aa)	-	-
ENST00000541399	NCAPD2-210	584	-	-	- (aa)	-	-
ENST00000545732	NCAPD2-213	543	-	-	- (aa)	-	-
ENST00000539084	NCAPD2-207	4290	-	ENSP00000438495	81 (aa)	-	F5H431
ENST00000315579	NCAPD2-201	5548	-	ENSP00000325017	1401 (aa)	-	Q15021
ENST00000535804	NCAPD2-203	537	-	-	- (aa)	-	-
ENST00000538600	NCAPD2-206	290	-	-	- (aa)	-	-
ENST00000539714	NCAPD2-208	533	-	ENSP00000444377	118 (aa)	-	F5GZK7

Gene Model

Click here to download ENSG00000010292's gene model file

Phenotypes

ensgID	Trait	pValue	Pubmed ID
ENSG00000010292	Gastrointestinal Neoplasms	5.7020000E-005	23504502

GWAS

ensgID	SNP	Chromosome	Position	SNP-risk	Trait	PubmedID	95% CI	Or or BEAT	EFO ID
ENSG00000010292	rs10849478	12	6512085	C	Blood protein levels	30072576	[NR] unit increase	0.7364076	EFO_0007937
ENSG00000010292	rs10849478	12	6512085	C	Blood protein levels	30072576	[0.084-0.182] unit increase	0.133	EFO_0007937

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000010292's network

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

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0000228	nuclear chromosome	12138188.	IDA	Component
GO:0000779	condensed chromosome, centromeric region	21873635.	IBA	Component
GO:0000793	condensed chromosome	12138188.	IDA	Component
GO:0000796	condensin complex	11136719.12138188.	IDA	Component
GO:0000797	condensin core heterodimer	10958694.	NAS	Component
GO:0000799	nuclear condensin complex	21873635.	IBA	Component
GO:0003682	chromatin binding	21873635.	IBA	Function
GO:0005515	protein binding	12138188.17268547.26496610.	IPI	Function
GO:0005634	nucleus	10958694.	NAS	Component
GO:0005654	nucleoplasm	-	IDA	Component
GO:0005737	cytoplasm	12138188.	IDA	Component
GO:0005737	cytoplasm	10958694.	NAS	Component
GO:0005829	cytosol	-	IDA	Component
GO:0005829	cytosol	-	TAS	Component
GO:0007076	mitotic chromosome condensation	21873635.	IBA	Process
GO:0007076	mitotic chromosome condensation	11136719.	IDA	Process
GO:0007076	mitotic chromosome condensation	27737959.	IMP	Process
GO:0007076	mitotic chromosome condensation	10958694.	NAS	Process
GO:0010032	meiotic chromosome condensation	21873635.	IBA	Process
GO:0016020	membrane	19946888.	HDA	Component
GO:0042393	histone binding	21873635.	IBA	Function
GO:0042393	histone binding	12138188.	IDA	Function
GO:0042393	histone binding	10958694.	NAS	Function
GO:0051301	cell division	-	IEA	Process
GO:0051304	chromosome separation	21873635.	IBA	Process

Differential Expression

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq
ACC	chr12	6530786	Silent	novel	Q1311Q	0.42
BLCA	chr12	6514370	Missense_Mutation	novel	L231F	0.35
BLCA	chr12	6529898	Missense_Mutation	novel	I1259M	0.52
BLCA	chr12	6528243	Silent	novel	R1072R	0.03
BLCA	chr12	6525673	Missense_Mutation	NA	L769V	0.43
BLCA	chr12	6528748	Silent	novel	D1123D	0.27
BLCA	chr12	6510471	Intron	novel		0.2
BLCA	chr12	6522999	Missense_Mutation	novel	A709D	0.23
BLCA	chr12	6517009	Missense_Mutation	rs369341180	R390Q	0.44
BLCA	chr12	6531473	3'UTR	novel		0.64
BLCA	chr12	6528715	Silent	rs149244253	A1112A	0.1
BLCA	chr12	6528984	Missense_Mutation	rs766002564	R1173C	0.17
BLCA	chr12	6517022	Missense_Mutation	NA	Q394H	0.17
BLCA	chr12	6517664	Missense_Mutation	NA	Q463H	0.13
BLCA	chr12	6528727	Missense_Mutation	novel	M1116I	0.35
BLCA	chr12	6514580	Missense_Mutation	NA	I278V	0.51
BLCA	chr12	6514480	Missense_Mutation	novel	I244M	0.44
BRCA	chr12	6522979	Silent	novel	L702L	0.1
BRCA	chr12	6521082	Silent	NA	L562L	0.26
BRCA	chr12	6522015	Missense_Mutation	NA	M644I	0.15
BRCA	chr12	6522847	Missense_Mutation	novel	E658D	0.08
BRCA	chr12	6517009	Missense_Mutation	rs369341180	R390Q	0.18
BRCA	chr12	6510334	Intron	rs771660530		0.29
BRCA	chr12	6526993	Missense_Mutation	novel	S946N	0.12
BRCA	chr12	6528274	Missense_Mutation	NA	L1082P	0.25
CESC	chr12	6530812	Missense_Mutation	NA	S1320C	0.27
CESC	chr12	6509779	Missense_Mutation	novel	Y64H	0.07
CESC	chr12	6509780	In_Frame_Ins	novel	Y64_S65insG	0.07
CESC	chr12	6516925	Missense_Mutation	NA	R362K	0.3
CESC	chr12	6525601	Missense_Mutation	novel	K745E	0.52
CESC	chr12	6526478	Missense_Mutation	novel	P866L	0.29
CESC	chr12	6529584	Missense_Mutation	rs771553945	R1215H	0.42
CESC	chr12	6527014	Missense_Mutation	novel	R953Q	0.33
CESC	chr12	6528835	Missense_Mutation	NA	F1152L	0.33
CESC	chr12	6495223	Missense_Mutation	novel	R42T	0.13
COAD	chr12	6522850	Missense_Mutation	NA	F659L	0.39
COAD	chr12	6510106	Nonsense_Mutation	novel	E79*	0.14
COAD	chr12	6527776	Splice_Site	novel	X970_splice	0.34
COAD	chr12	6528209	Silent	novel	F1060F	0.33
COAD	chr12	6528995	Silent	novel	D1176D	0.35
COAD	chr12	6509716	Splice_Site	novel	X43_splice	0.1
COAD	chr12	6528282	Missense_Mutation	rs199911941	R1085C	0.43
COAD	chr12	6529515	Missense_Mutation	novel	Q1192R	0.39
COAD	chr12	6530753	Silent	NA	I1300I	0.12
COAD	chr12	6528236	Silent	NA	P1069P	0.13
COAD	chr12	6525707	Missense_Mutation	NA	M780T	0.27
COAD	chr12	6510653	Missense_Mutation	novel	L96P	0.24
COAD	chr12	6528076	Missense_Mutation	novel	K1043R	0.14
COAD	chr12	6526307	Frame_Shift_Del	rs775519918	*F837Sfs36**	0.57
COAD	chr12	6526929	Missense_Mutation	novel	N925D	0.03
COAD	chr12	6526931	Silent	novel	N925N	0.03
COAD	chr12	6509728	Missense_Mutation	NA	A47T	0.34
COAD	chr12	6530721	Missense_Mutation	NA	R1290W	0.27
COAD	chr12	6522838	Missense_Mutation	novel	E655D	0.06
COAD	chr12	6522850	Missense_Mutation	NA	F659L	0.36
COAD	chr12	6510083	Missense_Mutation	rs200920120	R71Q	0.18
ESCA	chr12	6514286	Silent	novel	Y203Y	0.12
ESCA	chr12	6526155	Silent	novel	A812A	0.78
ESCA	chr12	6514316	Missense_Mutation	novel	H213Q	0.22
ESCA	chr12	6521005	Nonsense_Mutation	rs770092608	R537*	0.27
GBM	chr12	6526959	Silent	novel	L935L	0.25
GBM	chr12	6526943	Silent	novel	L929L	0.04
GBM	chr12	6521929	Missense_Mutation	novel	K616E	0.04
GBM	chr12	6528062	Silent	novel	S1038S	0.1
GBM	chr12	6514830	Silent	novel	G299G	0.46
GBM	chr12	6522912	Missense_Mutation	novel	P680H	0.43
GBM	chr12	6526898	Silent	novel	S914S	0.05
GBM	chr12	6528722	Missense_Mutation	novel	V1115M	0.47
GBM	chr12	6517645	Missense_Mutation	novel	L457S	0.18
GBM	chr12	6527026	Missense_Mutation	novel	E957A	0.06
GBM	chr12	6526914	Missense_Mutation	novel	T920A	0.48
HNSC	chr12	6529594	Splice_Site	novel	X1218_splice	0.26
HNSC	chr12	6528294	Missense_Mutation	novel	L1089V	0.29
HNSC	chr12	6510345	Intron	novel		0.14
HNSC	chr12	6510102	Silent	novel	L77L	0.13
HNSC	chr12	6529938	Frame_Shift_Del	novel	*A1274Pfs8**	0.19
HNSC	chr12	6514327	Missense_Mutation	novel	R217L	0.18
HNSC	chr12	6509765	Missense_Mutation	novel	H59P	0.19
HNSC	chr12	6529850	Missense_Mutation	novel	M1243I	0.82
HNSC	chr12	6522996	Missense_Mutation	novel	S708C	0.3
HNSC	chr12	6514910	Missense_Mutation	novel	L326P	0.35
HNSC	chr12	6526293	Missense_Mutation	rs562898088	L830V	0.3
KIRC	chr12	6510076	Missense_Mutation	NA	H69N	0.3
KIRP	chr12	6529577	Silent	NA	R1213R	0.17
KIRP	chr12	6528326	Splice_Region	NA	A1099A	0.23
KIRP	chr12	6530794	Missense_Mutation	NA	P1314Q	0.33
LGG	chr12	6526470	Silent	NA	L863L	0.07
LGG	chr12	6510083	Missense_Mutation	rs200920120	R71Q	0.15
LGG	chr12	6526989	Missense_Mutation	NA	V945L	0.56
LIHC	chr12	6530969	Missense_Mutation	novel	V1338A	0.4
LIHC	chr12	6509792	Missense_Mutation	novel	H68L	0.28
LUAD	chr12	6526156	Nonsense_Mutation	novel	Q813*	0.32
LUAD	chr12	6510713	Missense_Mutation	NA	A116V	0.05
LUAD	chr12	6531357	Missense_Mutation	rs747329947	T1384I	0.16
LUAD	chr12	6517461	Silent	novel	L428L	0.18
LUAD	chr12	6521868	Silent	NA	V595V	0.31
LUAD	chr12	6495194	Silent	NA	L32L	0.52
LUAD	chr12	6526455	Silent	novel	V858V	0.29
LUAD	chr12	6528049	Missense_Mutation	novel	S1034F	0.28
LUAD	chr12	6528204	Silent	novel	L1059L	0.27
LUAD	chr12	6510373	Intron	novel		0.04
LUAD	chr12	6514780	Nonsense_Mutation	novel	G283*	0.07
LUAD	chr12	6526320	Silent	NA	L839L	0.64
LUAD	chr12	6526344	Missense_Mutation	novel	E847Q	0.15
LUAD	chr12	6514921	Splice_Site	NA	X329_splice	0.39
LUSC	chr12	6527034	Missense_Mutation	novel	E960Q	0.1
LUSC	chr12	6516903	Nonsense_Mutation	novel	E355*	0.32
LUSC	chr12	6517871	Missense_Mutation	novel	E501K	0.1
LUSC	chr12	6526119	Silent	rs115791107	G800G	0.25
LUSC	chr12	6521059	Missense_Mutation	novel	E555Q	0.13
LUSC	chr12	6527970	Missense_Mutation	novel	K1008Q	0.04
LUSC	chr12	6521069	Missense_Mutation	novel	E558V	0.24
LUSC	chr12	6527025	Nonsense_Mutation	novel	E957*	0.07
LUSC	chr12	6510354	Intron	novel		0.16
LUSC	chr12	6510244	Intron	rs760296122		0.27
LUSC	chr12	6528788	Silent	NA	L1137L	0.36
LUSC	chr12	6528840	Missense_Mutation	rs199672478	N1154S	0.26
LUSC	chr12	6530793	Missense_Mutation	novel	P1314A	0.22
LUSC	chr12	6510700	Missense_Mutation	rs780825688	A112T	0.11
LUSC	chr12	6526126	Missense_Mutation	novel	E803K	0.22
LUSC	chr12	6531387	Missense_Mutation	rs773097640	A1394V	0.14
MESO	chr12	6510294	Intron	novel		0.49
OV	chr12	6526167	Silent	NA	C816C	0.41
OV	chr12	6526989	Missense_Mutation	NA	V945L	0.08
OV	chr12	6526941	Missense_Mutation	novel	L929M	0.06
OV	chr12	6528012	Missense_Mutation	novel	C1022S	0.04
OV	chr12	6528206	Silent	novel	L1059L	0.02
OV	chr12	6526967	Missense_Mutation	novel	Q937H	0.08
OV	chr12	6527001	Missense_Mutation	novel	L949V	0.11
OV	chr12	6527851	Missense_Mutation	novel	E994D	0.13
OV	chr12	6495092	5'UTR	novel		0.04
OV	chr12	6526978	Nonsense_Mutation	novel	L941*	0.05
OV	chr12	6516898	In_Frame_Ins	novel	Q353delinsHLP	0.24
OV	chr12	6516899	Nonsense_Mutation	novel	*L354Yfs5**	0.21
PAAD	chr12	6509751	Silent	novel	L54L	0.04
PAAD	chr12	6510699	Silent	rs754881441	N111N	0.16
PAAD	chr12	6514375	Missense_Mutation	rs754200286	R233H	0.09
PAAD	chr12	6517640	Missense_Mutation	novel	Q455H	0.17
PAAD	chr12	6527858	Missense_Mutation	rs750894814	R997C	0.16
PRAD	chr12	6510480	Intron	novel		0.21
PRAD	chr12	6516840	Missense_Mutation	rs762678605	R334C	0.31
PRAD	chr12	6517362	Splice_Region	novel		0.42
READ	chr12	6526894	Missense_Mutation	novel	E913V	0.1
READ	chr12	6528951	Missense_Mutation	rs746072942	A1162T	0.26
READ	chr12	6517642	Missense_Mutation	NA	K456T	0.24
READ	chr12	6510356	Intron	novel		0.4
SARC	chr12	6527858	Missense_Mutation	rs750894814	R997C	0.26
SARC	chr12	6526919	Silent	NA	F921F	0.29
SKCM	chr12	6528192	Missense_Mutation	NA	Q1055K	0.26
SKCM	chr12	6528198	Missense_Mutation	rs754648578	R1057C	0.39
SKCM	chr12	6522006	Silent	rs559407977	I641I	0.3
SKCM	chr12	6514911	Silent	NA	L326L	0.17
SKCM	chr12	6510529	Intron	novel		0.17
SKCM	chr12	6527857	Silent	NA	I996I	0.19
SKCM	chr12	6526476	Silent	novel	I865I	0.23
SKCM	chr12	6514793	Missense_Mutation	NA	P287L	0.26
SKCM	chr12	6526313	Silent	NA	P836P	0.29
SKCM	chr12	6510474	Intron	rs771378502		0.07
SKCM	chr12	6521906	Missense_Mutation	novel	S608F	0.45
SKCM	chr12	6522944	Missense_Mutation	novel	E691K	0.27
SKCM	chr12	6528235	Missense_Mutation	novel	P1069L	0.48
SKCM	chr12	6525670	Missense_Mutation	novel	P768S	0.45
SKCM	chr12	6514794	Silent	novel	P287P	0.42
SKCM	chr12	6531467	3'UTR	rs774544730		0.37
SKCM	chr12	6526911	Missense_Mutation	NA	P919S	0.56
SKCM	chr12	6527857	Silent	NA	I996I	0.3
SKCM	chr12	6510759	Missense_Mutation	NA	F131L	0.28
SKCM	chr12	6509734	Nonsense_Mutation	rs550146120	R49*	0.38
SKCM	chr12	6526919	Silent	NA	F921F	0.39
SKCM	chr12	6516923	Silent	novel	T361T	0.53
SKCM	chr12	6529841	Silent	NA	L1240L	0.34
SKCM	chr12	6509734	Nonsense_Mutation	rs550146120	R49*	0.45
SKCM	chr12	6521026	Nonsense_Mutation	novel	Q544*	0.12
SKCM	chr12	6514306	Missense_Mutation	rs756503239	T210I	0.52
STAD	chr12	6514803	Silent	NA	L290L	0.14
STAD	chr12	6510504	Intron	novel		0.29
STAD	chr12	6510743	Missense_Mutation	rs748909515	R126H	0.49
STAD	chr12	6510254	Intron	novel		0.39
STAD	chr12	6521995	Frame_Shift_Ins	novel	*G639Wfs9**	0.31
STAD	chr12	6516939	Missense_Mutation	novel	D367N	0.39
STAD	chr12	6529843	Missense_Mutation	rs145700246	R1241H	0.21
STAD	chr12	6528194	Missense_Mutation	NA	Q1055H	0.35
STAD	chr12	6527999	Silent	novel	L1017L	0.74
STAD	chr12	6530794	Missense_Mutation	NA	P1314Q	0.39
STAD	chr12	6525636	Silent	NA	L756L	0.11
STAD	chr12	6526901	Silent	novel	P915P	0.3
STAD	chr12	6514808	Missense_Mutation	rs150197479	R292Q	0.21
STAD	chr12	6528282	Missense_Mutation	rs199911941	R1085C	0.12
STAD	chr12	6521992	Missense_Mutation	NA	A637T	0.38
STAD	chr12	6528762	Missense_Mutation	NA	K1128R	0.2
STAD	chr12	6510629	Missense_Mutation	NA	V88A	0.17
THCA	chr12	6510405	Intron	novel		0.09
THYM	chr12	6531059	Missense_Mutation	novel	D1368G	0.17
UCEC	chr12	6510686	Missense_Mutation	NA	G107E	0.34
UCEC	chr12	6531033	Missense_Mutation	NA	K1359N	0.35
UCEC	chr12	6528783	Missense_Mutation	rs764924444	A1135V	0.14
UCEC	chr12	6529516	Missense_Mutation	novel	Q1192H	0.47
UCEC	chr12	6531468	3'UTR	novel		0.22
UCEC	chr12	6517427	Silent	novel	K416K	0.1
UCEC	chr12	6510774	Silent	novel	S136S	0.07
UCEC	chr12	6521006	Missense_Mutation	rs778277993	R537Q	0.6
UCEC	chr12	6531452	3'UTR	novel		0.32
UCEC	chr12	6522850	Missense_Mutation	NA	F659L	0.44
UCEC	chr12	6495171	Nonsense_Mutation	novel	Q25*	0.3
UCEC	chr12	6516935	Silent	novel	F365F	0.36
UCEC	chr12	6525616	Missense_Mutation	novel	P750S	0.31
UCEC	chr12	6517413	Missense_Mutation	rs201272617	R412C	0.23
UCEC	chr12	6517677	Missense_Mutation	novel	A468T	0.43
UCEC	chr12	6528715	Silent	rs149244253	A1112A	0.49
UCEC	chr12	6495146	Missense_Mutation	NA	E16D	0.2
UCEC	chr12	6525634	Missense_Mutation	NA	L756M	0.21
UCEC	chr12	6521005	Nonsense_Mutation	rs770092608	R537*	0.16
UCEC	chr12	6531326	Splice_Site	novel	X1374_splice	0.08
UCEC	chr12	6531047	Missense_Mutation	NA	V1364A	0.24
UCEC	chr12	6514463	Splice_Site	novel	X239_splice	0.22
UCEC	chr12	6516841	Missense_Mutation	rs771302335	R334H	0.16
UCEC	chr12	6527009	Silent	rs370594671	R951R	0.22
UCEC	chr12	6530755	Missense_Mutation	novel	K1301R	0.45
UCEC	chr12	6521830	Missense_Mutation	rs776884151	R583W	0.38
UCEC	chr12	6521996	Missense_Mutation	rs755462892	I638T	0.35
UCEC	chr12	6522850	Missense_Mutation	NA	F659L	0.34
UCEC	chr12	6510083	Missense_Mutation	rs200920120	R71Q	0.36
UCEC	chr12	6529516	Silent	novel	Q1192Q	0.3
UCEC	chr12	6531391	Silent	rs766471840	S1395S	0.69
UCEC	chr12	6495119	Silent	novel	E7E	0.42
UCEC	chr12	6514886	Missense_Mutation	novel	S318N	0.37
UCEC	chr12	6517027	Splice_Site	novel	X395_splice	0.52
UCEC	chr12	6521999	Missense_Mutation	novel	G639D	0.41
UCEC	chr12	6510294	Intron	novel		0.48
UCEC	chr12	6528963	Missense_Mutation	novel	L1166I	0.58
UCEC	chr12	6531561	3'UTR	novel		0.38
UCEC	chr12	6517671	Missense_Mutation	NA	T466A	0.35
UCEC	chr12	6521880	Missense_Mutation	NA	K599N	0.41
UCEC	chr12	6529813	Missense_Mutation	NA	S1231L	0.4
UCEC	chr12	6530974	Missense_Mutation	rs369464603	P1340S	0.41
UCEC	chr12	6521866	Missense_Mutation	novel	V595F	0.21
UCEC	chr12	6510225	Intron	novel		0.04
UCEC	chr12	6526613	Missense_Mutation	rs145781104	P911L	0.42
UCEC	chr12	6516916	Missense_Mutation	rs776764263	R359Q	0.36
UCEC	chr12	6521035	Missense_Mutation	rs200077145	E547K	0.48
UCEC	chr12	6526306	Frame_Shift_Ins	rs772347389	*F837Lfs11**	0.38
UCEC	chr12	6522903	Missense_Mutation	rs148424921	R677H	0.45
UCEC	chr12	6517009	Missense_Mutation	rs369341180	R390Q	0.26
UCEC	chr12	6528984	Missense_Mutation	rs766002564	R1173C	0.46
UCEC	chr12	6530791	Missense_Mutation	NA	A1313V	0.21
UCEC	chr12	6510700	Missense_Mutation	rs780825688	A112T	0.35
UCEC	chr12	6495189	Missense_Mutation	novel	V31I	0.31
UCEC	chr12	6517011	Missense_Mutation	novel	I391V	0.24
UCEC	chr12	6511151	Nonsense_Mutation	novel	W162*	0.39
UCEC	chr12	6526163	Missense_Mutation	novel	V815A	0.16
UCEC	chr12	6510304	Intron	novel		0.39
UCEC	chr12	6510356	Intron	novel		0.14
UCEC	chr12	6510764	Missense_Mutation	novel	T133I	0.17
UCEC	chr12	6511191	Silent	novel	L176L	0.35
UCEC	chr12	6525681	Silent	rs757787808	R771R	0.37
UCEC	chr12	6528047	Silent	novel	L1033L	0.38
UCEC	chr12	6528313	Missense_Mutation	novel	P1095H	0.21
UCEC	chr12	6528738	Missense_Mutation	novel	I1120T	0.19
UCEC	chr12	6522931	Silent	rs370930042	E686E	0.41
UCEC	chr12	6526897	Missense_Mutation	rs141629311	S914F	0.11
UCEC	chr12	6517940	Missense_Mutation	novel	L524I	0.33
UCEC	chr12	6517864	Silent	NA	Q498Q	0.3
UCEC	chr12	6522950	Missense_Mutation	rs775825528	V693M	0.25
UCEC	chr12	6523287	Missense_Mutation	novel	N719H	0.45

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
DLBC	DEL	0.1042	0.11856
MESO	DEL	0.0805	0.17495
PAAD	DEL	0.125	0.0019175
TGCT	AMP	0.9467	3.5918e-21
THYM	AMP	0.0325	0.24554

Survival Analysis

Cancer	P-value	Q-value
THYM	0.0026	Kaplan-Meier Survival Analysis
KIRC	0.0024	Kaplan-Meier Survival Analysis
STAD	0.0074	Kaplan-Meier Survival Analysis
SARC	0.00037	Kaplan-Meier Survival Analysis
MESO	0.00011	Kaplan-Meier Survival Analysis
SKCM	0.0021	Kaplan-Meier Survival Analysis
KIRP	0.00012	Kaplan-Meier Survival Analysis
PAAD	0.0032	Kaplan-Meier Survival Analysis
READ	0.032	Kaplan-Meier Survival Analysis
UCEC	0.0053	Kaplan-Meier Survival Analysis
LIHC	0.0001	Kaplan-Meier Survival Analysis
LUAD	0.00011	Kaplan-Meier Survival Analysis
UVM	0.0018	Kaplan-Meier Survival Analysis

Drugs

EuRBPDB

Description

RBPome

Expression

Transcripts

Gene Model

Phenotypes

GWAS

PPI

Gene Ontology

Select Dataset :

Input Drug :

Input Cell Line :

Eesembl ID

Cell lines and drugs in GSE70138 or GSE92742