EuRBPDB

Basic Information
Cancer Related Information

Description

RBPome

Expression

Transcripts

Gene Model

Pathways

Phenotypes

PPI

Orthologs

Gene Ontology

Description

Ensembl ID: ENSG00000076928 (Gene tree)
Gene ID: 9138
Gene Symbol: ARHGEF1
Alias: P115-RHOGEF|SUB1.5|LBCL2
Full Name: Rho guanine nucleotide exchange factor 1
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Plus strand
Length: 46,990 bases
Position: chr19:41,883,161-41,930,150
Accession: 681
RBP type: non-canonical RBP
Summary: Rho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein coupled receptors. The encoded protein may form complex with G proteins and stimulate Rho-dependent signals. Multiple alternatively spliced transcript variants have been found for this gene, but the full-length nature of some variants has not been defined. [provided by RefSeq, Jul 2008]

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
22658674	Insights into RNA biology from an atlas of mammalian mRNA-binding proteins	RIC & Hela	2012 May 31	Castello A	DOI: 10.1016/j.cell.2012.04.031
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
ENST00000617585	ARHGEF1-223	737	-	-	- (aa)	-	-
ENST00000598587	ARHGEF1-216	359	-	-	- (aa)	-	-
ENST00000599846	ARHGEF1-219	3393	-	ENSP00000470715	968 (aa)	-	M0QZR4
ENST00000594258	ARHGEF1-207	919	-	ENSP00000470042	307 (aa)	-	M0QYS3
ENST00000347545	ARHGEF1-202	3091	-	ENSP00000344429	879 (aa)	-	Q92888
ENST00000598444	ARHGEF1-215	425	-	-	- (aa)	-	-
ENST00000594513	ARHGEF1-209	325	-	-	- (aa)	-	-
ENST00000595897	ARHGEF1-213	2973	-	-	- (aa)	-	-
ENST00000354532	ARHGEF1-203	3243	-	ENSP00000346532	912 (aa)	-	Q92888
ENST00000596957	ARHGEF1-214	570	-	-	- (aa)	-	-
ENST00000599589	ARHGEF1-218	2636	-	ENSP00000469735	702 (aa)	-	M0QYC1
ENST00000593609	ARHGEF1-205	576	-	-	- (aa)	-	-
ENST00000594044	ARHGEF1-206	834	-	-	- (aa)	-	-
ENST00000600387	ARHGEF1-221	2272	-	-	- (aa)	-	-
ENST00000598812	ARHGEF1-217	588	-	ENSP00000473229	88 (aa)	-	M0R3H5
ENST00000378152	ARHGEF1-204	2986	-	ENSP00000367394	948 (aa)	-	Q92888
ENST00000594417	ARHGEF1-208	769	-	ENSP00000471942	128 (aa)	-	M0R1K8
ENST00000337665	ARHGEF1-201	3171	-	ENSP00000337261	927 (aa)	-	Q92888
ENST00000594521	ARHGEF1-210	826	-	ENSP00000470557	275 (aa)	-	M0QZH8
ENST00000595723	ARHGEF1-211	872	-	ENSP00000472466	291 (aa)	-	M0R2C7
ENST00000595770	ARHGEF1-212	663	NR_135626	-	- (aa)	-	-
ENST00000600274	ARHGEF1-220	3439	-	-	- (aa)	-	-
ENST00000600517	ARHGEF1-222	428	-	ENSP00000469409	68 (aa)	-	M0QXV6

Gene Model

Click here to download ENSG00000076928's gene model file

Pathways

Pathway ID	Pathway Name	Source
hsa04270	Vascular smooth muscle contraction	KEGG
hsa04611	Platelet activation	KEGG
hsa04810	Regulation of actin cytoskeleton	KEGG
hsa04928	Parathyroid hormone synthesis, secretion and action	KEGG
hsa05163	Human cytomegalovirus infection	KEGG
hsa05200	Pathways in cancer	KEGG
hsa05205	Proteoglycans in cancer	KEGG

Phenotypes

ensgID	Trait	pValue	Pubmed ID
ENSG00000076928	Body Height	4.6056322927704E-10	17903300
ENSG00000076928	Body Height	4.92245488132124E-9	17903300
ENSG00000076928	Body Height	2.32580733047009E-7	17903300
ENSG00000076928	Body Height	4.39096805994889E-9	17903300
ENSG00000076928	Hypertension	6.9647986E-006	-

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000076928'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
ENSG00000076928	ARHGEF1	99	89.364	ENSMUSG00000040940	Arhgef1	98	91.304	Mus_musculus

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0001664	G protein-coupled receptor binding	-	IEA	Function
GO:0003723	RNA binding	22658674.	HDA	Function
GO:0005089	Rho guanyl-nucleotide exchange factor activity	-	IEA	Function
GO:0005096	GTPase activator activity	-	IEA	Function
GO:0005515	protein binding	12681510.20300064.25416956.	IPI	Function
GO:0005737	cytoplasm	10747909.	TAS	Component
GO:0005829	cytosol	-	IDA	Component
GO:0005829	cytosol	-	TAS	Component
GO:0005886	plasma membrane	-	IDA	Component
GO:0007186	G protein-coupled receptor signaling pathway	-	TAS	Process
GO:0007266	Rho protein signal transduction	10747909.	TAS	Process
GO:0008283	cell proliferation	8810315.	TAS	Process
GO:0035023	regulation of Rho protein signal transduction	-	IEA	Process
GO:0043065	positive regulation of apoptotic process	-	TAS	Process
GO:0043547	positive regulation of GTPase activity	-	IEA	Process
GO:0051056	regulation of small GTPase mediated signal transduction	-	TAS	Process

Cancer associated literatures

PID	Title	Article	Time	Author	Doi
26911374	Cdc42 and Rac1 activity is reduced in human pheochromocytoma and correlates with FARP1 and ARHGEF1 expression.	Endocr Relat Cancer	2016 Apr	Crois?? P	doi: 10.1530/ERC-15-0502
12748184	Hyaluronan-mediated CD44 interaction with RhoGEF and Rho kinase promotes Grb2-associated binder-1 phosphorylation and phosphatidylinositol 3-kinase signaling leading to cytokine (macrophage-colony stimulating factor) production and breast tumor progression.	J Biol Chem	2003 Aug 8	Bourguignon LY	-
23070684	miR-143 inhibits the metastasis of pancreatic cancer and an associated signaling pathway.	Tumour Biol	2012 Dec	Hu Y	doi: 10.1007/s13277-012-0446-8

Differential Expression

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq
ACC	chr19	41906751	Missense_Mutation	novel	G902W	0.23
BLCA	chr19	41906791	3'UTR	novel		0.31
BLCA	chr19	41888758	Missense_Mutation	novel	E40K	0.44
BLCA	chr19	41906492	Missense_Mutation	NA	E843K	0.37
BLCA	chr19	41888099	Missense_Mutation	rs183598386	R6P	0.14
BLCA	chr19	41895399	Missense_Mutation	rs781882065	R310W	0.35
BLCA	chr19	41905947	Missense_Mutation	rs376841668	E805K	0.24
BLCA	chr19	41888099	Missense_Mutation	rs183598386	R6Q	0.18
BLCA	chr19	41892206	Intron	novel		0.22
BLCA	chr19	41903712	Silent	novel	L615L	0.2
BLCA	chr19	41902562	Silent	novel	Q509Q	0.09
BLCA	chr19	41904288	Missense_Mutation	novel	S689C	0.13
BLCA	chr19	41903309	Missense_Mutation	NA	E581K	0.19
BLCA	chr19	41898553	Silent	NA	P411P	0.3
BRCA	chr19	41923195	Missense_Mutation	novel	K657M	0.13
BRCA	chr19	41906495	Missense_Mutation	NA	D844Y	0.39
BRCA	chr19	41905211	Silent	NA	L762L	0.43
BRCA	chr19	41898375	Intron	novel		0.46
BRCA	chr19	41895420	Missense_Mutation	NA	P317S	0.16
BRCA	chr19	41884461	Intron	novel		0.22
BRCA	chr19	41892052	Missense_Mutation	NA	G85C	0.39
BRCA	chr19	41888261	Missense_Mutation	NA	E32Q	0.16
BRCA	chr19	41892794	Nonsense_Mutation	NA	E187*	0.45
BRCA	chr19	41888273	Missense_Mutation	NA	E36Q	0.27
BRCA	chr19	41892122	Missense_Mutation	NA	A108V	0.13
BRCA	chr19	41888217	Missense_Mutation	NA	G17D	0.39
BRCA	chr19	41906622	Splice_Site	NA	X885_splice	0.24
CESC	chr19	41928978	Missense_Mutation	novel	Y97S	0.31
CESC	chr19	41892487	Intron	NA		0.52
CESC	chr19	41892848	Missense_Mutation	novel	Q205K	0.18
CESC	chr19	41892849	Missense_Mutation	novel	Q205R	0.18
CESC	chr19	41894503	Missense_Mutation	novel	S266N	0.42
CESC	chr19	41907427	3'UTR	novel		0.45
CESC	chr19	41895383	Silent	rs782392629	G304G	0.07
CESC	chr19	41903387	Missense_Mutation	novel	R607S	0.29
CESC	chr19	41907189	3'UTR	rs542363730		0.71
COAD	chr19	41898529	Silent	rs200140005	P403P	0.24
COAD	chr19	41906771	Silent	NA	Q908Q	0.25
COAD	chr19	41892022	Splice_Region	novel		0.28
COAD	chr19	41902558	Missense_Mutation	novel	F508Y	0.35
COAD	chr19	41902627	Missense_Mutation	NA	R531H	0.35
COAD	chr19	41888804	Missense_Mutation	rs782343511	R55H	0.32
COAD	chr19	41896394	Missense_Mutation	novel	E345K	0.33
COAD	chr19	41905793	Silent	rs376174015	N790N	0.15
COAD	chr19	41906537	Frame_Shift_Del	NA	*G859Afs4**	0.32
COAD	chr19	41896482	Missense_Mutation	novel	S374I	0.15
COAD	chr19	41902809	Missense_Mutation	NA	R550H	0.3
COAD	chr19	41896386	Frame_Shift_Del	NA	*L344Wfs12**	0.31
COAD	chr19	41892644	Missense_Mutation	novel	R137W	0.43
COAD	chr19	41894227	Missense_Mutation	novel	I222T	0.13
COAD	chr19	41905936	Splice_Region	rs368319532		0.19
COAD	chr19	41896445	Missense_Mutation	rs781864535	P362S	0.58
COAD	chr19	41901995	Missense_Mutation	novel	N459S	0.36
COAD	chr19	41894479	Missense_Mutation	novel	P258L	0.3
COAD	chr19	41896386	Frame_Shift_Del	NA	*L344Wfs12**	0.32
COAD	chr19	41906794	3'UTR	rs369026490		0.25
COAD	chr19	41905946	Silent	rs144745694	T804T	0.18
COAD	chr19	41892043	Missense_Mutation	rs374342194	D82N	0.31
DLBC	chr19	41906592	Missense_Mutation	novel	S876N	0.17
ESCA	chr19	41898244	Intron	novel		0.09
ESCA	chr19	41907193	3'UTR	novel		0.47
ESCA	chr19	41904317	Missense_Mutation	novel	D699H	0.2
ESCA	chr19	41896773	Intron	novel		0.27
ESCA	chr19	41902342	Missense_Mutation	NA	V495M	0.56
GBM	chr19	41905784	Missense_Mutation	novel	S787R	0.08
GBM	chr19	41892816	Missense_Mutation	rs529943853	A194V	0.56
GBM	chr19	41903406	Missense_Mutation	novel	L613Q	0.28
GBM	chr19	41894471	Silent	rs782763644	S255S	0.54
HNSC	chr19	41901886	Splice_Site	novel	X423_splice	0.2
HNSC	chr19	41904098	Missense_Mutation	novel	D661Y	0.15
HNSC	chr19	41905763	Silent	novel	T780T	0.31
HNSC	chr19	41902644	Frame_Shift_Del	novel	*A538Rfs14**	0.43
HNSC	chr19	41902818	Missense_Mutation	novel	Q553L	0.27
HNSC	chr19	41894453	In_Frame_Del	novel	M250_E257del	0.34
HNSC	chr19	41893301	Missense_Mutation	novel	K214N	0.31
HNSC	chr19	41902812	Missense_Mutation	novel	R551H	0.21
HNSC	chr19	41895373	Missense_Mutation	rs200700112	R301Q	0.19
KIRC	chr19	41904347	Missense_Mutation	NA	R709W	0.4
KIRC	chr19	41892073	Missense_Mutation	novel	A92P	0.22
LGG	chr19	41892108	Silent	rs782384716	F103F	0.5
LGG	chr19	41892817	Silent	rs781919682	A194A	0.33
LIHC	chr19	41904962	Silent	novel	F725F	0.27
LIHC	chr19	41892801	In_Frame_Ins	novel	H192_R196dup	0.35
LUAD	chr19	41892206	Intron	novel		0.07
LUAD	chr19	41894629	Missense_Mutation	NA	P282L	0.69
LUAD	chr19	41906578	Missense_Mutation	novel	Q871H	0.24
LUAD	chr19	41888232	Missense_Mutation	NA	S22I	0.26
LUAD	chr19	41884451	Intron	rs545498995		0.17
LUAD	chr19	41892144	Intron	rs782802836		0.25
LUAD	chr19	41892814	Silent	NA	V193V	0.45
LUAD	chr19	41884437	Intron	novel		0.07
LUAD	chr19	41903772	Silent	NA	L635L	0.36
LUAD	chr19	41888082	5'UTR	novel		0.41
LUAD	chr19	41895414	Missense_Mutation	novel	G315R	0.08
LUAD	chr19	41906542	Silent	NA	G859G	0.26
LUSC	chr19	41895473	Silent	NA	P334P	0.2
LUSC	chr19	41892329	Splice_Site	NA	X109_splice	0.16
LUSC	chr19	41892739	Missense_Mutation	novel	W168C	0.08
LUSC	chr19	41892731	Missense_Mutation	novel	T166A	0.47
LUSC	chr19	41888279	Splice_Site	novel	X37_splice	0.26
LUSC	chr19	41901885	Splice_Site	novel	X423_splice	0.11
LUSC	chr19	41892228	Intron	novel		0.08
LUSC	chr19	41906499	Missense_Mutation	rs782293753	N845S	0.42
LUSC	chr19	41892343	Missense_Mutation	NA	P113S	0.23
OV	chr19	41892605	Missense_Mutation	NA	R124G	0.28
OV	chr19	41884474	Intron	NA		0.33
OV	chr19	41888821	Missense_Mutation	NA	A61T	0.39
OV	chr19	41892790	Missense_Mutation	novel	S185R	0.67
OV	chr19	41905814	Silent	rs149372116	T797T	0.13
OV	chr19	41894257	Missense_Mutation	NA	R232Q	0.2
OV	chr19	41905191	Missense_Mutation	NA	T756P	0.31
OV	chr19	41905177	Missense_Mutation	novel	W751S	0.31
OV	chr19	41896674	Intron	NA		0.38
PAAD	chr19	41892805	Missense_Mutation	novel	E190D	0.22
PAAD	chr19	41902342	Missense_Mutation	NA	V495M	0.16
PRAD	chr19	41906786	Nonstop_Mutation	NA	913Cext19	0.37
PRAD	chr19	41888800	Missense_Mutation	rs782110668	R54W	0.41
PRAD	chr19	41905219	Missense_Mutation	novel	P765L	0.47
READ	chr19	41892671	Nonsense_Mutation	novel	Q146*	0.33
SARC	chr19	41892166	Intron	novel		0.35
SARC	chr19	41892167	Intron	novel		0.38
SKCM	chr19	41892232	Intron	novel		0.31
SKCM	chr19	41888097	Silent	novel	A5A	0.43
SKCM	chr19	41906792	3'UTR	novel		0.52
SKCM	chr19	41895445	Missense_Mutation	NA	S325F	0.29
SKCM	chr19	41895461	Silent	novel	S330S	0.22
SKCM	chr19	41902573	Missense_Mutation	rs781854393	S513F	0.3
SKCM	chr19	41892333	Splice_Region	NA	V109V	0.37
SKCM	chr19	41894297	Silent	NA	F245F	0.45
SKCM	chr19	41892649	Silent	rs782354288	F138F	0.5
SKCM	chr19	41892649	Silent	rs782354288	F138F	0.4
SKCM	chr19	41892720	Missense_Mutation	NA	L162P	0.25
SKCM	chr19	41905967	Silent	novel	L811L	0.16
STAD	chr19	41894481	Missense_Mutation	NA	A259S	0.29
STAD	chr19	41901912	Silent	rs377396950	H431H	0.31
STAD	chr19	41902653	Missense_Mutation	NA	V540M	0.35
STAD	chr19	41906487	Missense_Mutation	rs375950739	A841V	0.27
STAD	chr19	41898564	Missense_Mutation	NA	V415A	0.62
STAD	chr19	41892336	Silent	rs782791739	L110L	0.08
STAD	chr19	41892049	Silent	NA	L84L	0.36
STAD	chr19	41892289	Intron	novel		0.07
STAD	chr19	41903318	Missense_Mutation	NA	E584K	0.14
STAD	chr19	41893293	Missense_Mutation	NA	E212K	0.17
STAD	chr19	41902800	Missense_Mutation	NA	P547L	0.19
STAD	chr19	41902348	Silent	NA	L497L	0.37
STAD	chr19	41895424	Missense_Mutation	novel	G318V	0.29
STAD	chr19	41895396	Missense_Mutation	NA	S309P	0.35
STAD	chr19	41905234	Missense_Mutation	rs781883859	R770H	0.42
UCEC	chr19	41888266	Silent	rs41306984	N33N	0.45
UCEC	chr19	41904271	Silent	rs782266591	E683E	0.19
UCEC	chr19	41923142	Silent	novel	A639A	0.43
UCEC	chr19	41905256	Silent	NA	P777P	0.5
UCEC	chr19	41892661	Silent	NA	V142V	0.22
UCEC	chr19	41902289	Missense_Mutation	rs782431103	R477H	0.52
UCEC	chr19	41907440	3'UTR	novel		0.48
UCEC	chr19	41892733	Silent	NA	T166T	0.32
UCEC	chr19	41898515	Missense_Mutation	NA	R399W	0.28
UCEC	chr19	41902024	Missense_Mutation	NA	E469K	0.21
UCEC	chr19	41894272	Missense_Mutation	novel	D237V	0.22
UCEC	chr19	41895480	Nonsense_Mutation	novel	E337*	0.14
UCEC	chr19	41892777	Missense_Mutation	rs782691132	R181Q	0.15
UCEC	chr19	41902652	Silent	novel	F539F	0.05
UCEC	chr19	41902803	Missense_Mutation	novel	R548Q	0.48
UCEC	chr19	41894281	Missense_Mutation	rs368940793	S240L	0.43
UCEC	chr19	41895477	Missense_Mutation	rs782364939	R336W	0.4
UCEC	chr19	41906572	Missense_Mutation	novel	E869D	0.49
UCEC	chr19	41896726	Intron	novel		0.24
UCEC	chr19	41902797	Missense_Mutation	rs781793791	R546H	0.54
UCEC	chr19	41894475	Missense_Mutation	rs782629121	E257K	0.33
UCEC	chr19	41896462	Silent	rs199929341	D367D	0.45
UCEC	chr19	41902289	Missense_Mutation	rs782431103	R477H	0.47
UCEC	chr19	41902886	Missense_Mutation	rs782335508	G576R	0.37
UCEC	chr19	41898515	Missense_Mutation	NA	R399W	0.14
UCEC	chr19	41892606	Missense_Mutation	NA	R124H	0.22
UCEC	chr19	41907427	3'UTR	novel		0.13
UCEC	chr19	41892649	Silent	rs782354288	F138F	0.27
UCEC	chr19	41888211	Missense_Mutation	rs781793490	R15Q	0.53
UCEC	chr19	41903316	Missense_Mutation	novel	T583K	0.5
UCEC	chr19	41892361	Missense_Mutation	rs371771035	A119T	0.37
UCEC	chr19	41895384	Missense_Mutation	rs201550936	V305M	0.39
UCEC	chr19	41884475	Intron	novel		0.24
UCEC	chr19	41896386	Frame_Shift_Del	NA	*L344Wfs12**	0.34
UCEC	chr19	41898324	Intron	novel		0.33
UCEC	chr19	41896386	Frame_Shift_Del	NA	*L344Wfs12**	0.7
UCEC	chr19	41902335	Silent	novel	I492I	0.14
UCEC	chr19	41923135	Missense_Mutation	novel	M637T	0.32
UCEC	chr19	41888266	Silent	rs41306984	N33N	0.36
UCEC	chr19	41903398	Missense_Mutation	novel	E610D	0.09
UCEC	chr19	41892316	Intron	novel		0.5
UCEC	chr19	41894281	Missense_Mutation	rs368940793	S240L	0.44
UCEC	chr19	41896526	Intron	novel		0.53
UCEC	chr19	41904964	Missense_Mutation	NA	Y726C	0.54
UCEC	chr19	41893278	Missense_Mutation	novel	T207A	0.4
UCEC	chr19	41898334	Intron	novel		0.29
UCEC	chr19	41895405	Missense_Mutation	rs782161306	R312W	0.15
UCEC	chr19	41894464	Missense_Mutation	novel	R253L	0.38
UCEC	chr19	41905178	Missense_Mutation	NA	W751C	0.31
UCEC	chr19	41902800	Missense_Mutation	NA	P547L	0.44
UCEC	chr19	41892802	Silent	novel	R189R	0.53
UCEC	chr19	41888277	Missense_Mutation	novel	T37I	0.15
UCEC	chr19	41894449	Splice_Site	novel	X249_splice	0.1
UCEC	chr19	41898422	Intron	novel		0.4
UCEC	chr19	41892776	Missense_Mutation	rs782100845	R181W	0.36
UCEC	chr19	41892308	Intron	novel		0.36
UCEC	chr19	41888094	Silent	NA	F4F	0.2
UCEC	chr19	41894276	Missense_Mutation	novel	K238N	0.17
UCEC	chr19	41901952	Missense_Mutation	novel	P445S	0.43
UCEC	chr19	41902617	Missense_Mutation	novel	A528T	0.5
UCEC	chr19	41906541	Missense_Mutation	rs782700907	G859D	0.42
UCEC	chr19	41892605	Missense_Mutation	rs369826806	R124C	0.26
UCEC	chr19	41892605	Missense_Mutation	rs369826806	R124C	0.38
UCEC	chr19	41906020	Missense_Mutation	rs782226783	R829Q	0.47
UCEC	chr19	41928950	Missense_Mutation	novel	G702E	0.3
UCEC	chr19	41907394	3'UTR	novel		0.31

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
KIRP	DEL	0.0451	0.054726
READ	DEL	0.0606	0.23023
UCS	DEL	0.2143	0.12448

Survival Analysis

Cancer	P-value	Q-value
THYM	0.0038	Kaplan-Meier Survival Analysis
KIRC	0.0001	Kaplan-Meier Survival Analysis
MESO	0.047	Kaplan-Meier Survival Analysis
ACC	0.00069	Kaplan-Meier Survival Analysis
UCS	0.0046	Kaplan-Meier Survival Analysis
HNSC	0.041	Kaplan-Meier Survival Analysis
LUSC	0.021	Kaplan-Meier Survival Analysis
BRCA	0.0016	Kaplan-Meier Survival Analysis
ESCA	0.044	Kaplan-Meier Survival Analysis
KIRP	0.0087	Kaplan-Meier Survival Analysis
COAD	0.0065	Kaplan-Meier Survival Analysis
PAAD	0.015	Kaplan-Meier Survival Analysis
LAML	0.00098	Kaplan-Meier Survival Analysis
KICH	0.049	Kaplan-Meier Survival Analysis
UCEC	0.013	Kaplan-Meier Survival Analysis
OV	0.027	Kaplan-Meier Survival Analysis

Drugs

EuRBPDB

Description

RBPome

Expression

Transcripts

Gene Model

Pathways

Phenotypes

PPI

Orthologs

Gene Ontology

Select Dataset :

Input Drug :

Input Cell Line :

Eesembl ID

Cell lines and drugs in GSE70138 or GSE92742