EuRBPDB

Basic Information
Cancer Related Information

Description

RBPome

Expression

Transcripts

Gene Model

Phenotypes

GWAS

PPI

Orthologs

Gene Ontology

Description

Ensembl ID: ENSG00000050405 (Gene tree)
Gene ID: 51474
Gene Symbol: LIMA1
Alias: EPLIN
Full Name: LIM domain and actin binding 1
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Minus strand
Length: 107,791 bases
Position: chr12:50,175,780-50,283,570
Accession: 24636
RBP type: non-canonical RBP
Summary: This gene encodes a cytoskeleton-associated protein that inhibits actin filament depolymerization and cross-links filaments in bundles. It is downregulated in some cancer cell lines. Alternatively spliced transcript variants encoding different isoforms have been described for this gene, and expression of some of the variants maybe independently regulated. [provided by RefSeq, Aug 2011]

RNA binding proteome (RBPome)

PID	Title	Method	Time	Author	Doi
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
27453046	Comprehensive Identification of RNA-Binding Domains in Human Cells	RIC & Hela	2016 Aug 18	Castello A	DOI: 10.1016/j.molcel.2016.06.029

Expression

Transcripts

Transcript ID	Name	Length	RefSeq ID	Protein ID	Length	RefSeq ID	UniportKB ID
ENST00000552491	LIMA1-212	2652	-	ENSP00000448463	456 (aa)	-	F8VS07
ENST00000552823	LIMA1-215	3254	-	ENSP00000450266	599 (aa)	-	Q9UHB6
ENST00000551486	LIMA1-207	587	-	-	- (aa)	-	-
ENST00000552045	LIMA1-210	386	-	-	- (aa)	-	-
ENST00000552008	LIMA1-209	566	-	-	- (aa)	-	-
ENST00000552720	LIMA1-213	2457	-	ENSP00000448411	388 (aa)	-	F8VRN8
ENST00000550611	LIMA1-206	543	-	-	- (aa)	-	-
ENST00000551691	LIMA1-208	583	-	ENSP00000447975	130 (aa)	-	F8VTU2
ENST00000550592	LIMA1-205	567	-	ENSP00000449890	111 (aa)	-	F8VVQ7
ENST00000341247	LIMA1-201	3706	-	ENSP00000340184	759 (aa)	-	Q9UHB6
ENST00000394943	LIMA1-202	3669	XM_011538455	ENSP00000378400	760 (aa)	XP_011536757	Q9UHB6
ENST00000547825	LIMA1-203	3920	XM_017019429	ENSP00000448706	457 (aa)	XP_016874918	Q9UHB6
ENST00000549064	LIMA1-204	648	-	-	- (aa)	-	-
ENST00000552909	LIMA1-216	2162	-	ENSP00000450087	598 (aa)	-	F8VQE1
ENST00000552338	LIMA1-211	555	-	-	- (aa)	-	-
ENST00000552783	LIMA1-214	3612	-	ENSP00000448779	600 (aa)	-	Q9UHB6

Gene Model

Click here to download ENSG00000050405's gene model file

Phenotypes

ensgID	Trait	pValue	Pubmed ID
ENSG00000050405	Echocardiography	4.01082721609348E-6	17903301
ENSG00000050405	Echocardiography	9.78048970368356E-8	17903301
ENSG00000050405	Echocardiography	1.01770834392633E-7	17903301
ENSG00000050405	Intelligence Tests	2.9409800E-005	-
ENSG00000050405	Child Development Disorders, Pervasive	4.9777200E-005	-
ENSG00000050405	Colorectal Neoplasms	3E-8	24737748
ENSG00000050405	Colorectal Neoplasms	3E-6	26621817
ENSG00000050405	Endometrial Neoplasms	3E-6	26621817
ENSG00000050405	Schizophrenia	5E-6	26198764

GWAS

ensgID	SNP	Chromosome	Position	SNP-risk	Trait	PubmedID	95% CI	Or or BEAT	EFO ID
ENSG00000050405	rs12817211	12	50185615	C	Colorectal or endometrial cancer	26621817	[1.07-1.18]	1.12	EFO_0005842\|EFO_0004230
ENSG00000050405	rs4459386	12	50201164	A	Schizophrenia	26198764	[NR]	1.05	EFO_0000692
ENSG00000050405	rs34245511	12	50179650	C	Colorectal cancer	24737748	[NR]	1.144	EFO_0005842
ENSG00000050405	rs4883481	12	50180528	?	Systolic blood pressure	30595370			EFO_0006335
ENSG00000050405	rs2302900	12	50205926	?	White blood cell count	30595370			EFO_0004308
ENSG00000050405	rs4883482	12	50183134	?	Cardiovascular disease	30595370			EFO_0000319
ENSG00000050405	rs2160994	12	50256274	?	Eosinophil counts	30595370			EFO_0004842

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000050405'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
ENSG00000050405	LIMA1	98	82.569	ENSMUSG00000023022	Lima1	100	82.569	Mus_musculus

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0001725	stress fiber	10618726.	IDA	Component
GO:0001726	ruffle	-	ISS	Component
GO:0003785	actin monomer binding	12566430.	IDA	Function
GO:0005515	protein binding	18093941.20309963.24694988.29880681.	IPI	Function
GO:0005829	cytosol	-	IDA	Component
GO:0005886	plasma membrane	-	IDA	Component
GO:0005925	focal adhesion	21423176.	HDA	Component
GO:0005925	focal adhesion	10618726.24694988.	IDA	Component
GO:0008203	cholesterol metabolic process	-	IEA	Process
GO:0015629	actin cytoskeleton	-	IDA	Component
GO:0016477	cell migration	-	ISS	Process
GO:0030299	intestinal cholesterol absorption	-	ISS	Process
GO:0030835	negative regulation of actin filament depolymerization	12566430.	IDA	Process
GO:0031526	brush border membrane	-	ISS	Component
GO:0031529	ruffle organization	12566430.	IDA	Process
GO:0032154	cleavage furrow	20309963.	IDA	Component
GO:0042632	cholesterol homeostasis	-	ISS	Process
GO:0045296	cadherin binding	25468996.	HDA	Function
GO:0046872	metal ion binding	-	IEA	Function
GO:0051015	actin filament binding	12566430.	IDA	Function
GO:0051017	actin filament bundle assembly	12566430.	IDA	Process

Cancer associated literatures

PID	Title	Article	Time	Author	Doi
28465438	Human phosphatase CDC14A regulates actin organization through dephosphorylation of epithelial protein lost in neoplasm.	Proc Natl Acad Sci U S A	2017 May 16	Chen NP	doi: 10.1073/pnas.1619356114
18796137	Eplin-alpha expression in human breast cancer, the impact on cellular migration and clinical outcome.	Mol Cancer	2008 Sep 16	Jiang WG	doi: 10.1186/1476-4598-7-71.
22493360	EPLIN-α expression in human oesophageal cancer and its impact on cellular aggressiveness and clinical outcome.	Anticancer Res	2012 Apr	Liu Y	-
23188829	Epidermal growth factor promotes protein degradation of epithelial protein lost in neoplasm (EPLIN), a putative metastasis suppressor, during epithelial-mesenchymal transition.	J Biol Chem	2013 Jan 18	Zhang S	doi: 10.1074/jbc.M112.438341
21625216	EPLIN downregulation promotes epithelial-mesenchymal transition in prostate cancer cells and correlates with clinical lymph node metastasis.	Oncogene	2011 Dec 15	Zhang S	doi: 10.1038/onc.2011.199
27035883	Epithelial protein lost in neoplasm-α (EPLIN-α) is a potential prognostic marker for the progression of epithelial ovarian cancer.	Int J Oncol	2016 Jun	Liu R	doi: 10.3892/ijo.2016.3462
30098000	Mechanistic insights of epithelial protein lost in neoplasm in prostate cancer metastasis.	Int J Cancer	2018 Nov 15	Collins RJ	doi: 10.1002/ijc.31786

Differential Expression

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq
BLCA	chr12	50192540	Missense_Mutation	novel	E351G	0.28
BLCA	chr12	50222250	Missense_Mutation	rs749831700	P134L	0.33
BLCA	chr12	50222343	Frame_Shift_Del	novel	*I97Sfs4**	0.14
BLCA	chr12	50204632	Missense_Mutation	NA	L262V	0.45
BLCA	chr12	50181942	Silent	novel	I412I	0.32
BLCA	chr12	50177855	Missense_Mutation	NA	P497S	0.35
BLCA	chr12	50178064	Missense_Mutation	novel	G427V	0.08
BLCA	chr12	50177871	Silent	NA	P491P	0.25
BLCA	chr12	50177124	Silent	NA	L740L	0.18
BLCA	chr12	50222240	Silent	rs769930517	L137L	0.12
BLCA	chr12	50222365	Nonsense_Mutation	NA	E96*	0.09
BLCA	chr12	50177689	Nonsense_Mutation	NA	S552*	0.14
BLCA	chr12	50200798	Silent	novel	I317I	0.09
BLCA	chr12	50248660	Missense_Mutation	NA	S31L	0.46
BLCA	chr12	50248668	Missense_Mutation	NA	K28N	0.44
BRCA	chr12	50177679	Silent	novel	K555K	0.43
BRCA	chr12	50177404	Missense_Mutation	NA	N647S	0.12
BRCA	chr12	50177738	Frame_Shift_Ins	novel	*T536Hfs2**	0.08
BRCA	chr12	50204644	Missense_Mutation	NA	E258Q	0.24
BRCA	chr12	50222686	Intron	novel		0.09
BRCA	chr12	50177760	Silent	NA	L528L	0.17
BRCA	chr12	50222473	Missense_Mutation	NA	L60V	0.2
BRCA	chr12	50222686	Intron	novel		0.13
BRCA	chr12	50204593	Missense_Mutation	novel	Q275K	0.1
BRCA	chr12	50222686	Intron	novel		0.14
BRCA	chr12	50222073	Missense_Mutation	novel	P193Q	0.07
BRCA	chr12	50195866	Missense_Mutation	novel	L332M	0.19
BRCA	chr12	50177072	Missense_Mutation	NA	E758K	0.15
BRCA	chr12	50200860	Missense_Mutation	rs763276725	E297K	0.21
BRCA	chr12	50200899	Intron	novel		0.19
BRCA	chr12	50177199	Missense_Mutation	novel	F715L	0.11
BRCA	chr12	50177835	Silent	NA	V503V	0.21
CESC	chr12	50177630	Missense_Mutation	rs781115938	D572N	0.19
CESC	chr12	50182031	Missense_Mutation	NA	Q383E	0.36
CESC	chr12	50231680	Missense_Mutation	NA	M50I	0.12
CESC	chr12	50192529	Missense_Mutation	novel	P355S	0.53
COAD	chr12	50177397	Silent	NA	G649G	0.44
COAD	chr12	50177096	Missense_Mutation	rs766724186	R750W	0.09
COAD	chr12	50178040	Missense_Mutation	NA	R435I	0.1
COAD	chr12	50248688	Nonsense_Mutation	NA	E22*	0.34
COAD	chr12	50231700	Missense_Mutation	NA	A44T	0.04
COAD	chr12	50177513	Missense_Mutation	novel	P611S	0.38
COAD	chr12	50177737	Missense_Mutation	novel	T536I	0.06
COAD	chr12	50234212	Intron	novel		0.86
COAD	chr12	50222686	Intron	novel		0.17
COAD	chr12	50234212	Intron	novel		0.61
COAD	chr12	50177739	Frame_Shift_Del	NA	*T536Lfs38**	0.28
COAD	chr12	50177578	Missense_Mutation	NA	R589H	0.31
COAD	chr12	50177739	Frame_Shift_Del	NA	*T536Lfs38**	0.53
COAD	chr12	50200911	Intron	rs768847562		0.22
COAD	chr12	50192514	Missense_Mutation	NA	P360S	0.24
COAD	chr12	50222532	Intron	novel		0.04
COAD	chr12	50176897	3'UTR	novel		0.29
COAD	chr12	50222209	Missense_Mutation	NA	G148S	0.28
COAD	chr12	50222110	Missense_Mutation	novel	T181A	0.22
COAD	chr12	50234212	Intron	novel		0.71
COAD	chr12	50178040	Missense_Mutation	NA	R435I	0.34
COAD	chr12	50177192	Nonsense_Mutation	rs776901156	E718*	0.3
COAD	chr12	50177028	3'UTR	rs777671959		0.39
ESCA	chr12	50200778	Missense_Mutation	novel	K324R	0.14
ESCA	chr12	50177669	Missense_Mutation	novel	E559K	0.14
ESCA	chr12	50222379	Missense_Mutation	rs770526598	R91Q	0.73
GBM	chr12	50222033	Silent	novel	P206P	0.13
GBM	chr12	50181973	Missense_Mutation	rs200141288	R402H	0.06
GBM	chr12	50177041	3'UTR	novel		0.23
GBM	chr12	50200902	Intron	novel		0.15
HNSC	chr12	50177981	Missense_Mutation	novel	G455S	0.04
HNSC	chr12	50200932	Intron	novel		0.27
HNSC	chr12	50222273	Silent	novel	P126P	0.17
HNSC	chr12	50222481	Missense_Mutation	novel	T57I	0.21
HNSC	chr12	50177013	3'UTR	novel		0.29
HNSC	chr12	50200859	Missense_Mutation	novel	E297G	0.48
HNSC	chr12	50200856	Missense_Mutation	novel	I298T	0.19
KICH	chr12	50234212	Intron	novel		0.19
KIRC	chr12	50222346	Missense_Mutation	NA	D102V	0.14
KIRC	chr12	50177439	Silent	NA	Q635Q	0.22
KIRC	chr12	50195880	Missense_Mutation	novel	A327G	0.04
KIRC	chr12	50222248	Nonsense_Mutation	novel	E135*	0.03
KIRC	chr12	50222250	Frame_Shift_Ins	novel	*P134Lfs36**	0.03
KIRC	chr12	50177949	Nonsense_Mutation	NA	W465*	0.2
KIRP	chr12	50177552	Frame_Shift_Ins	novel	*Q598Sfs26**	0.5
KIRP	chr12	50177632	Frame_Shift_Del	novel	*V571Afs3**	0.36
KIRP	chr12	50200838	Missense_Mutation	novel	E304G	0.21
KIRP	chr12	50177728	Missense_Mutation	NA	G539A	0.48
LAML	chr12	50177576	Missense_Mutation	novel	P590T	0.04
LGG	chr12	50204653	Nonsense_Mutation	NA	R255*	0.44
LGG	chr12	50195857	Missense_Mutation	rs373214767	R335C	0.11
LGG	chr12	50192498	Missense_Mutation	NA	S365F	0.07
LIHC	chr12	50181973	Missense_Mutation	novel	R402L	0.21
LUAD	chr12	50248668	Missense_Mutation	novel	K28N	0.1
LUAD	chr12	50192465	Missense_Mutation	novel	P376L	0.25
LUAD	chr12	50192466	Missense_Mutation	novel	P376T	0.26
LUAD	chr12	50177695	Missense_Mutation	novel	K550T	0.22
LUAD	chr12	50200829	Missense_Mutation	NA	E307V	0.16
LUAD	chr12	50222424	Missense_Mutation	novel	W76L	0.25
LUAD	chr12	50177552	Missense_Mutation	NA	Q598E	0.12
LUAD	chr12	50177801	Missense_Mutation	NA	Q515E	0.14
LUAD	chr12	50195829	Splice_Site	rs778142224	X344_splice	0.07
LUAD	chr12	50204630	Silent	novel	L262L	0.27
LUSC	chr12	50177927	Missense_Mutation	NA	E473Q	0.05
LUSC	chr12	50248744	Missense_Mutation	novel	S3L	0.25
LUSC	chr12	50177975	Missense_Mutation	novel	G457W	0.22
LUSC	chr12	50248669	Missense_Mutation	NA	K28R	0.59
LUSC	chr12	50176897	3'UTR	novel		0.42
LUSC	chr12	50192484	Missense_Mutation	novel	L370V	0.15
LUSC	chr12	50248656	Silent	rs773649764	S32S	0.12
LUSC	chr12	50177470	Missense_Mutation	novel	S625F	0.22
OV	chr12	50222576	Intron	novel		0.05
OV	chr12	50222686	Intron	novel		0.16
OV	chr12	50222686	Intron	novel		0.17
OV	chr12	50200865	Missense_Mutation	novel	G295A	0.06
OV	chr12	50200867	Missense_Mutation	novel	S294R	0.06
OV	chr12	50248727	Missense_Mutation	rs780877633	R9W	0.21
OV	chr12	50177843	Missense_Mutation	novel	V501M	0.06
PAAD	chr12	50181975	Silent	novel	E401E	0.07
PAAD	chr12	50182021	Missense_Mutation	novel	A386V	0.05
PAAD	chr12	50222272	Missense_Mutation	novel	R127G	0.2
READ	chr12	50177375	Nonsense_Mutation	NA	E657*	0.27
READ	chr12	50177096	Missense_Mutation	rs766724186	R750W	0.4
READ	chr12	50222112	Missense_Mutation	novel	N180S	0.4
READ	chr12	50222420	Missense_Mutation	novel	E77D	0.36
READ	chr12	50177465	Missense_Mutation	NA	G627R	0.12
SKCM	chr12	50177666	Missense_Mutation	NA	D560N	0.33
SKCM	chr12	50204638	Missense_Mutation	NA	P260S	0.9
SKCM	chr12	50222158	Silent	NA	L165L	0.22
SKCM	chr12	50222256	Nonsense_Mutation	rs768965142	S132*	0.5
SKCM	chr12	50177182	Missense_Mutation	novel	T721I	0.64
SKCM	chr12	50177700	Frame_Shift_Del	novel	*A544Dfs11**	0.27
SKCM	chr12	50200968	Intron	novel		0.4
SKCM	chr12	50181933	Silent	novel	F415F	0.29
SKCM	chr12	50248748	Missense_Mutation	rs772093224	E2K	0.25
SKCM	chr12	50248749	Translation_Start_Site	novel	M1?	0.25
SKCM	chr12	50192524	Silent	novel	V356V	0.47
SKCM	chr12	50195848	Missense_Mutation	NA	P338S	0.27
SKCM	chr12	50222376	Frame_Shift_Del	novel	*N92Tfs17**	0.24
STAD	chr12	50222232	Missense_Mutation	NA	G140D	0.31
STAD	chr12	50182008	Silent	rs760289112	C390C	0.14
STAD	chr12	50200906	Intron	novel		0.3
STAD	chr12	50177021	3'UTR	novel		0.2
STAD	chr12	50200932	Intron	novel		0.19
STAD	chr12	50192474	Missense_Mutation	novel	S373N	0.47
STAD	chr12	50222317	Missense_Mutation	rs146061384	A112T	0.28
STAD	chr12	50222357	Missense_Mutation	novel	R98S	0.05
STAD	chr12	50177244	Missense_Mutation	novel	Q700H	0.15
STAD	chr12	50222170	Frame_Shift_Del	NA	*M161Wfs5**	0.32
STAD	chr12	50204669	Missense_Mutation	NA	E249D	0.31
STAD	chr12	50177522	Missense_Mutation	NA	V608M	0.05
THCA	chr12	50192554	In_Frame_Ins	novel	S346_Q347insGKQN	0.08
UCEC	chr12	50195842	Missense_Mutation	rs781719966	E340K	0.38
UCEC	chr12	50222076	Missense_Mutation	NA	V192A	0.31
UCEC	chr12	50222344	Missense_Mutation	NA	H103N	0.27
UCEC	chr12	50176933	3'UTR	rs565878967		0.16
UCEC	chr12	50200962	Intron	novel		0.32
UCEC	chr12	50176505	3'UTR	novel		0.44
UCEC	chr12	50177781	Silent	novel	K521K	0.39
UCEC	chr12	50200911	Intron	rs768847562		0.38
UCEC	chr12	50234204	Intron	NA		0.54
UCEC	chr12	50222465	Missense_Mutation	novel	Q62H	0.23
UCEC	chr12	50176956	3'UTR	novel		0.45
UCEC	chr12	50222068	Missense_Mutation	novel	N195Y	0.57
UCEC	chr12	50181992	Missense_Mutation	novel	T396P	0.34
UCEC	chr12	50222096	Silent	rs747245139	G185G	0.07
UCEC	chr12	50222271	Missense_Mutation	novel	R127K	0.34
UCEC	chr12	50222370	Missense_Mutation	novel	S94I	0.41
UCEC	chr12	50177105	Missense_Mutation	novel	K747Q	0.08
UCEC	chr12	50176922	3'UTR	novel		0.22
UCEC	chr12	50177096	Missense_Mutation	rs766724186	R750W	0.21
UCEC	chr12	50222419	Frame_Shift_Ins	novel	*N78Gfs23**	0.14
UCEC	chr12	50222096	Silent	rs747245139	G185G	0.09
UCEC	chr12	50177973	Silent	NA	G457G	0.33
UCEC	chr12	50177323	Missense_Mutation	rs140187635	M674T	0.18
UCEC	chr12	50177676	Nonsense_Mutation	NA	W556*	0.49
UCEC	chr12	50176547	3'UTR	novel		0.26
UCEC	chr12	50204608	Nonsense_Mutation	rs767754461	R270*	0.2
UCEC	chr12	50177605	Missense_Mutation	rs772821365	R580Q	0.44
UCEC	chr12	50206062	Missense_Mutation	rs199735854	R213W	0.41
UCEC	chr12	50177676	Nonsense_Mutation	NA	W556*	0.1
UCEC	chr12	50176547	3'UTR	novel		0.42
UCEC	chr12	50177793	Missense_Mutation	novel	E517D	0.39
UCEC	chr12	50204608	Nonsense_Mutation	rs767754461	R270*	0.4
UCEC	chr12	50177428	Missense_Mutation	novel	A639D	0.06
UCEC	chr12	50176657	3'UTR	novel		0.4
UCEC	chr12	50177243	Nonsense_Mutation	novel	E701*	0.34
UCEC	chr12	50177630	Missense_Mutation	rs781115938	D572N	0.38
UCEC	chr12	50206027	Silent	novel	I224I	0.39
UCEC	chr12	50248657	Missense_Mutation	rs148884366	S32L	0.32
UCEC	chr12	50200819	Silent	NA	P310P	0.26
UCEC	chr12	50181987	Silent	novel	V397V	0.18
UCEC	chr12	50200913	Intron	novel		0.2
UCEC	chr12	50181902	Splice_Site	novel	X425_splice	0.53
UCEC	chr12	50176898	3'UTR	novel		0.17
UCEC	chr12	50177630	Missense_Mutation	rs781115938	D572N	0.48
UCEC	chr12	50177816	Missense_Mutation	novel	A510T	0.23
UCEC	chr12	50177428	Missense_Mutation	NA	A639V	0.07
UCEC	chr12	50222209	Missense_Mutation	NA	G148S	0.06
UCEC	chr12	50177931	Silent	rs146071798	N471N	0.31
UCEC	chr12	50248688	Nonsense_Mutation	NA	E22*	0.22
UCEC	chr12	50200861	Silent	rs764042104	G296G	0.46
UCEC	chr12	50204608	Nonsense_Mutation	rs767754461	R270*	0.5
UCEC	chr12	50222150	Missense_Mutation	novel	E167D	0.15
UCEC	chr12	50177858	Missense_Mutation	NA	A496T	0.25
UCEC	chr12	50177044	3'UTR	novel		0.32
UCEC	chr12	50181970	Missense_Mutation	novel	L403R	0.4
UCS	chr12	50177375	Nonsense_Mutation	NA	E657*	0.32

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
DLBC	AMP	0.1458	0.085003
READ	DEL	0.0545	0.064633
STAD	DEL	0.0998	0.22179

Survival Analysis

Cancer	P-value	Q-value
THYM	0.01	Kaplan-Meier Survival Analysis
KIRC	0.00014	Kaplan-Meier Survival Analysis
ACC	0.013	Kaplan-Meier Survival Analysis
HNSC	0.00011	Kaplan-Meier Survival Analysis
PAAD	0.0036	Kaplan-Meier Survival Analysis
UVM	0.012	Kaplan-Meier Survival Analysis

Drugs

EuRBPDB

Description

RBPome

Expression

Transcripts

Gene Model

Phenotypes

GWAS

PPI

Orthologs

Gene Ontology

Select Dataset :

Input Drug :

Input Cell Line :

Eesembl ID

Cell lines and drugs in GSE70138 or GSE92742