EuRBPDB

Note: to get the extension of tumor abbreviations.

Cancer Related Information
Basic Information

Cancer associated literatures

PID	Title	Article	Time	Author	Doi
22144583	MicroRNA-200c represses migration and invasion of breast cancer cells by targeting actin-regulatory proteins FHOD1 and PPM1F.	Mol Cell Biol	2012 Feb	Jurmeister S	doi: 10.1128/MCB.06212-11

Differential Expression

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq
ACC	chr16	67234215	Silent	novel	P496P	0.5
BLCA	chr16	67229945	Missense_Mutation	novel	S1087F	0.31
BLCA	chr16	67247417	5'UTR	novel		0.39
BLCA	chr16	67229894	Missense_Mutation	NA	S1104L	0.05
BLCA	chr16	67239444	Missense_Mutation	NA	C71S	0.13
BLCA	chr16	67230225	Missense_Mutation	NA	E1019Q	0.07
BLCA	chr16	67231231	Missense_Mutation	NA	S875C	0.13
BLCA	chr16	67230063	Splice_Region	novel		0.3
BLCA	chr16	67237274	Missense_Mutation	NA	D320N	0.28
BLCA	chr16	67229709	Missense_Mutation	rs762626115	T1141M	0.14
BLCA	chr16	67247271	Missense_Mutation	novel	G47E	0.73
BLCA	chr16	67229583	3'UTR	novel		0.3
BLCA	chr16	67229686	Missense_Mutation	novel	D1149N	0.24
BRCA	chr16	67237706	Silent	novel	N235N	0.11
BRCA	chr16	67231708	Missense_Mutation	NA	A772S	0.42
BRCA	chr16	67231808	Silent	NA	T738T	0.11
BRCA	chr16	67236637	Silent	novel	G413G	0.14
BRCA	chr16	67234116	Missense_Mutation	NA	I529M	0.45
BRCA	chr16	67229611	3'UTR	novel		0.75
BRCA	chr16	67237679	Silent	novel	V244V	0.07
BRCA	chr16	67229705	Missense_Mutation	NA	L1142F	0.23
BRCA	chr16	67231523	Silent	NA	L804L	0.14
BRCA	chr16	67247395	Missense_Mutation	NA	D6Y	0.13
CESC	chr16	67231344	Silent	NA	S837S	0.18
CESC	chr16	67234177	Missense_Mutation	rs771435032	R509Q	0.32
CESC	chr16	67234375	Missense_Mutation	NA	E473K	0.31
CESC	chr16	67229874	Missense_Mutation	NA	L1111V	0.34
CESC	chr16	67230132	Missense_Mutation	NA	H1050N	0.26
CESC	chr16	67230215	Nonsense_Mutation	NA	S1022*	0.18
CESC	chr16	67234466	Silent	novel	R442R	0.15
CESC	chr16	67238377	Splice_Region	rs751368196		0.3
CESC	chr16	67234093	Missense_Mutation	novel	P537H	0.3
CESC	chr16	67229844	Missense_Mutation	novel	R1121C	0.33
CESC	chr16	67237308	Silent	NA	A308A	0.51
CESC	chr16	67236999	Missense_Mutation	novel	G370D	0.17
CESC	chr16	67237537	Silent	novel	L263L	0.11
COAD	chr16	67237739	Frame_Shift_Ins	NA	*L225Afs46**	0.24
COAD	chr16	67238090	Missense_Mutation	NA	G196R	0.19
COAD	chr16	67234365	Missense_Mutation	rs373548373	G476E	0.45
COAD	chr16	67236620	Missense_Mutation	novel	N419I	0.11
COAD	chr16	67238614	Intron	novel		0.5
COAD	chr16	67230403	Missense_Mutation	rs747061959	R988W	0.36
COAD	chr16	67230402	Missense_Mutation	novel	R988Q	0.22
COAD	chr16	67237536	Missense_Mutation	NA	L263P	0.25
COAD	chr16	67236720	Missense_Mutation	NA	A386T	0.33
COAD	chr16	67230111	Silent	novel	L1057L	0.35
COAD	chr16	67236982	Missense_Mutation	NA	R376C	0.39
COAD	chr16	67231343	Missense_Mutation	novel	G838S	0.26
COAD	chr16	67236606	Missense_Mutation	rs765946969	I424V	0.32
COAD	chr16	67237320	Missense_Mutation	novel	Q304H	0.27
COAD	chr16	67237070	Silent	novel	G346G	0.38
COAD	chr16	67237298	Missense_Mutation	NA	R312C	0.33
COAD	chr16	67237060	Missense_Mutation	novel	R350W	0.15
COAD	chr16	67237764	Missense_Mutation	rs766104962	R216H	0.18
COAD	chr16	67238305	Missense_Mutation	NA	E148D	0.08
COAD	chr16	67236679	Silent	NA	L399L	0.37
COAD	chr16	67231207	Missense_Mutation	novel	A883V	0.11
COAD	chr16	67234178	Nonsense_Mutation	rs369969027	R509*	0.14
COAD	chr16	67236982	Missense_Mutation	NA	R376C	0.44
COAD	chr16	67236667	Silent	rs746990896	P403P	0.37
COAD	chr16	67232137	Missense_Mutation	rs773788569	A702T	0.22
COAD	chr16	67234193	Silent	NA	L504L	0.26
COAD	chr16	67238912	Missense_Mutation	NA	A122T	0.16
COAD	chr16	67230394	Silent	novel	R991R	0.35
ESCA	chr16	67230625	Missense_Mutation	novel	I945T	0.76
ESCA	chr16	67231785	Missense_Mutation	rs774658881	R746Q	0.36
ESCA	chr16	67232078	Silent	novel	L721L	0.05
ESCA	chr16	67234155	Silent	novel	K516K	0.17
GBM	chr16	67236573	Missense_Mutation	rs774140986	E435K	0.29
GBM	chr16	67238756	Intron	novel		0.33
GBM	chr16	67233758	Missense_Mutation	novel	P649S	0.14
GBM	chr16	67238756	Intron	novel		0.23
GBM	chr16	67237496	Nonsense_Mutation	novel	Y276*	0.18
GBM	chr16	67237547	Silent	novel	L259L	0.11
HNSC	chr16	67237352	Frame_Shift_Ins	novel	*F294Gfs29**	0.18
HNSC	chr16	67229810	Missense_Mutation	rs777850281	R1132H	0.25
HNSC	chr16	67230465	Missense_Mutation	rs190207170	A967V	0.24
HNSC	chr16	67238414	Missense_Mutation	rs754648916	R136H	0.21
HNSC	chr16	67238269	Silent	novel	E160E	0.36
HNSC	chr16	67233985	Nonsense_Mutation	novel	S573*	0.11
HNSC	chr16	67231191	Silent	novel	A888A	0.15
HNSC	chr16	67230711	Silent	novel	L916L	0.21
HNSC	chr16	67238273	Missense_Mutation	rs372756034	S159L	0.14
HNSC	chr16	67238448	Splice_Site	novel	X125_splice	0.14
HNSC	chr16	67229906	Missense_Mutation	novel	P1100H	0.29
HNSC	chr16	67238363	Intron	novel		0.11
HNSC	chr16	67238364	Intron	novel		0.11
KIRC	chr16	67230426	Missense_Mutation	rs772896045	L980P	0.14
KIRC	chr16	67231276	Missense_Mutation	NA	L860R	0.13
KIRP	chr16	67230457	Missense_Mutation	rs746053817	E970K	0.15
LGG	chr16	67230351	Missense_Mutation	NA	R1005H	0.17
LGG	chr16	67230447	Missense_Mutation	novel	I973S	0.32
LGG	chr16	67229567	3'UTR	novel		0.29
LGG	chr16	67231317	In_Frame_Del	novel	K846del	0.48
LGG	chr16	67230388	Nonsense_Mutation	novel	R993*	0.38
LGG	chr16	67238129	Splice_Site	novel	X183_splice	0.07
LGG	chr16	67238434	Silent	novel	S129S	0.52
LGG	chr16	67234088	Missense_Mutation	novel	L539F	0.39
LIHC	chr16	67234086	Silent	NA	L539L	0.33
LIHC	chr16	67247270	Silent	novel	G47G	0.21
LIHC	chr16	67231227	Silent	novel	D876D	0.77
LIHC	chr16	67229897	Missense_Mutation	novel	T1103I	0.29
LIHC	chr16	67230444	Missense_Mutation	novel	M974T	0.25
LUAD	chr16	67247471	5'UTR	novel		0.43
LUAD	chr16	67247324	Missense_Mutation	NA	F29L	0.46
LUAD	chr16	67230437	Missense_Mutation	NA	F976L	0.1
LUAD	chr16	67237322	Missense_Mutation	novel	Q304E	0.24
LUAD	chr16	67247471	5'UTR	novel		0.16
LUAD	chr16	67234029	Silent	NA	L558L	0.1
LUAD	chr16	67229588	3'UTR	novel		0.42
LUAD	chr16	67237302	Silent	novel	V310V	0.13
LUAD	chr16	67237481	Missense_Mutation	novel	I281M	0.17
LUAD	chr16	67231240	Missense_Mutation	NA	P872R	0.26
LUAD	chr16	67231767	Missense_Mutation	NA	A752V	0.27
LUSC	chr16	67231730	Silent	rs138688169	A764A	0.47
LUSC	chr16	67238342	Intron	novel		0.14
LUSC	chr16	67230195	Missense_Mutation	novel	P1029A	0.39
LUSC	chr16	67238249	Missense_Mutation	novel	R167L	0.71
LUSC	chr16	67230617	Missense_Mutation	novel	R948C	0.19
LUSC	chr16	67234123	Missense_Mutation	rs2271290	E527G	0.21
LUSC	chr16	67233978	Silent	novel	P575P	0.55
LUSC	chr16	67231778	Silent	novel	K748K	0.34
LUSC	chr16	67230491	Silent	novel	L958L	0.72
LUSC	chr16	67230118	Missense_Mutation	NA	K1054N	0.15
OV	chr16	67237036	Missense_Mutation	novel	S358P	0.44
OV	chr16	67237309	Frame_Shift_Del	novel	*A308Gfs27**	0.25
OV	chr16	67247263	Missense_Mutation	NA	P50A	0.63
OV	chr16	67237374	Silent	rs752207424	A286A	0.54
OV	chr16	67238528	Intron	novel		0.16
OV	chr16	67238045	Missense_Mutation	novel	C211R	0.12
PAAD	chr16	67239367	Missense_Mutation	novel	G97S	0.11
PRAD	chr16	67237056	Missense_Mutation	rs766805526	R351Q	0.45
PRAD	chr16	67230184	Silent	NA	P1032P	0.33
PRAD	chr16	67238883	Intron	novel		0.07
PRAD	chr16	67232137	Missense_Mutation	rs773788569	A702T	0.08
PRAD	chr16	67230476	Silent	NA	Y963Y	0.14
PRAD	chr16	67230665	Missense_Mutation	NA	F932L	0.15
PRAD	chr16	67229823	Missense_Mutation	novel	R1128C	0.39
READ	chr16	67237258	Missense_Mutation	NA	T325M	0.32
SARC	chr16	67236628	Silent	novel	A416A	0.54
SKCM	chr16	67233961	Frame_Shift_Del	novel	*G581Efs47**	0.35
SKCM	chr16	67231272	Silent	NA	H861H	0.4
SKCM	chr16	67238208	Missense_Mutation	NA	L181F	0.89
SKCM	chr16	67230479	Silent	NA	G962G	0.33
SKCM	chr16	67247419	5'UTR	novel		0.38
SKCM	chr16	67247420	5'UTR	novel		0.35
SKCM	chr16	67236656	Missense_Mutation	novel	P407L	0.33
SKCM	chr16	67230149	Missense_Mutation	rs746584932	R1044Q	0.31
SKCM	chr16	67233925	Missense_Mutation	NA	P593L	0.81
SKCM	chr16	67230682	Missense_Mutation	rs750277750	R926H	0.26
SKCM	chr16	67234116	Silent	NA	I529I	0.52
SKCM	chr16	67231296	Silent	rs143498229	T853T	0.38
SKCM	chr16	67237687	Missense_Mutation	NA	R242S	0.3
SKCM	chr16	67247395	Missense_Mutation	NA	D6N	0.29
SKCM	chr16	67239427	Missense_Mutation	NA	P77S	0.12
SKCM	chr16	67230225	Missense_Mutation	NA	E1019K	0.7
SKCM	chr16	67230362	Silent	NA	Q1001Q	0.29
SKCM	chr16	67229889	Missense_Mutation	NA	E1106K	0.33
SKCM	chr16	67232152	Missense_Mutation	novel	P697S	0.5
SKCM	chr16	67232153	Silent	novel	D696D	0.49
SKCM	chr16	67229881	Missense_Mutation	NA	M1108I	0.19
SKCM	chr16	67230627	Silent	rs111846078	R944R	0.36
STAD	chr16	67229882	Missense_Mutation	rs757132766	M1108T	0.23
STAD	chr16	67231639	Missense_Mutation	rs772102709	R795W	0.3
STAD	chr16	67234183	Missense_Mutation	NA	A507V	0.26
STAD	chr16	67233752	Missense_Mutation	rs143431266	A651T	0.23
STAD	chr16	67237012	Missense_Mutation	NA	R366C	0.52
STAD	chr16	67230457	Missense_Mutation	rs746053817	E970K	0.17
STAD	chr16	67237014	Missense_Mutation	novel	R365H	0.33
STAD	chr16	67237297	Missense_Mutation	novel	R312H	0.25
STAD	chr16	67236997	Missense_Mutation	NA	G371R	0.05
STAD	chr16	67238457	Intron	novel		0.41
STAD	chr16	67237730	Silent	NA	L227L	0.05
STAD	chr16	67230351	Missense_Mutation	NA	R1005H	0.09
STAD	chr16	67237658	Splice_Region	NA	T251T	0.07
STAD	chr16	67231292	Missense_Mutation	rs772252359	R855C	0.1
STAD	chr16	67237742	Silent	rs373272675	L223L	0.22
UCEC	chr16	67247338	Missense_Mutation	novel	D25Y	0.33
UCEC	chr16	67229553	3'UTR	novel		0.2
UCEC	chr16	67231786	Missense_Mutation	rs761974488	R746W	0.16
UCEC	chr16	67238411	Missense_Mutation	rs779437165	R137H	0.22
UCEC	chr16	67238913	Silent	rs751354160	N121N	0.48
UCEC	chr16	67247337	Missense_Mutation	novel	D25G	0.08
UCEC	chr16	67238843	Intron	novel		0.36
UCEC	chr16	67231231	Missense_Mutation	rs757925016	S875F	0.57
UCEC	chr16	67231796	Silent	novel	T742T	0.21
UCEC	chr16	67236666	Missense_Mutation	novel	A404T	0.41
UCEC	chr16	67229708	Silent	rs200812024	T1141T	0.51
UCEC	chr16	67229916	Missense_Mutation	novel	S1097T	0.09
UCEC	chr16	67230410	Silent	novel	L985L	0.18
UCEC	chr16	67237236	Splice_Region	novel		0.32
UCEC	chr16	67236691	Silent	novel	T395T	0.52
UCEC	chr16	67238313	Splice_Region	novel		0.18
UCEC	chr16	67238791	Intron	novel		0.09
UCEC	chr16	67234452	Missense_Mutation	NA	V447A	0.18
UCEC	chr16	67238478	Intron	novel		0.04
UCEC	chr16	67229802	Missense_Mutation	rs770847586	R1135C	0.34
UCEC	chr16	67236639	Missense_Mutation	rs780244054	G413S	0.29
UCEC	chr16	67230628	Missense_Mutation	novel	R944K	0.16
UCEC	chr16	67236983	Silent	novel	A375A	0.08
UCEC	chr16	67229643	Missense_Mutation	NA	E1163G	0.51
UCEC	chr16	67231291	Missense_Mutation	rs748331837	R855H	0.36
UCEC	chr16	67234422	Missense_Mutation	rs761027309	A457V	0.25
UCEC	chr16	67234178	Nonsense_Mutation	rs369969027	R509*	0.46
UCEC	chr16	67238888	Intron	novel		0.06
UCEC	chr16	67236639	Missense_Mutation	NA	G413C	0.23
UCEC	chr16	67230645	Silent	novel	R938R	0.34
UCEC	chr16	67232055	Missense_Mutation	novel	S729N	0.25
UCEC	chr16	67237110	Missense_Mutation	novel	A333V	0.28
UCEC	chr16	67230616	Missense_Mutation	NA	R948H	0.41
UCEC	chr16	67237011	Missense_Mutation	rs781228896	R366H	0.45
UCEC	chr16	67238736	Intron	novel		0.56
UCEC	chr16	67237261	Missense_Mutation	NA	R324H	0.43
UCEC	chr16	67237570	Splice_Site	NA	X252_splice	0.39
UCEC	chr16	67231759	Missense_Mutation	novel	A755S	0.51
UCEC	chr16	67229811	Missense_Mutation	rs775105803	R1132C	0.32
UCEC	chr16	67231714	Missense_Mutation	novel	T770A	0.07
UCEC	chr16	67236648	Missense_Mutation	novel	P410T	0.42
UCEC	chr16	67238096	Missense_Mutation	novel	M194V	0.42
UCEC	chr16	67230192	Frame_Shift_Ins	rs762098881	*S1030Qfs19**	0.23
UCEC	chr16	67230617	Missense_Mutation	novel	R948C	0.43
UCEC	chr16	67237261	Missense_Mutation	NA	R324H	0.42
UCEC	chr16	67233867	Silent	novel	H612H	0.43
UCEC	chr16	67234134	Silent	novel	S523S	0.08
UCEC	chr16	67231291	Missense_Mutation	rs748331837	R855H	0.14
UCEC	chr16	67229947	Silent	NA	P1086P	0.04
UCEC	chr16	67239455	Splice_Site	novel	X68_splice	0.5
UCEC	chr16	67230217	Missense_Mutation	NA	F1021L	0.58
UCEC	chr16	67234215	Silent	novel	P496P	0.35
UCEC	chr16	67238277	Missense_Mutation	novel	H158Y	0.29
UCEC	chr16	67229810	Missense_Mutation	rs777850281	R1132H	0.3
UCEC	chr16	67231344	Silent	NA	S837S	0.25
UCEC	chr16	67237747	Missense_Mutation	NA	A222T	0.29
UCEC	chr16	67234055	Missense_Mutation	novel	G550W	0.23
UCEC	chr16	67237047	Missense_Mutation	novel	R354Q	0.61
UCEC	chr16	67236690	Missense_Mutation	rs775259952	G396S	0.32
UCEC	chr16	67237674	Missense_Mutation	novel	S246Y	0.48
UCEC	chr16	67229414	3'UTR	novel		0.19
UCEC	chr16	67231241	Missense_Mutation	novel	P872S	0.21
UCEC	chr16	67247402	Silent	novel	G3G	0.42
UCEC	chr16	67239381	Missense_Mutation	rs757610175	R92Q	0.67
UCEC	chr16	67236992	Frame_Shift_Ins	novel	*C373Lfs59**	0.35
UCEC	chr16	67238777	Intron	novel		0.17
UCEC	chr16	67237380	Splice_Region	rs147795243	T284T	0.35

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
BLCA	AMP	0.1814	0.063591
CHOL	DEL	0.1667	0.23475
LAML	DEL	0.0314	0.0010312
TGCT	AMP	0.12	0.035574
UCEC	DEL	0.2783	4.7164e-05

Survival Analysis

Cancer	P-value	Q-value
THYM	0.032	Kaplan-Meier Survival Analysis
KIRC	0.0031	Kaplan-Meier Survival Analysis
SARC	0.0015	Kaplan-Meier Survival Analysis
MESO	0.022	Kaplan-Meier Survival Analysis
ACC	0.003	Kaplan-Meier Survival Analysis
HNSC	0.016	Kaplan-Meier Survival Analysis
SKCM	0.0049	Kaplan-Meier Survival Analysis
PRAD	0.022	Kaplan-Meier Survival Analysis
LUSC	0.00083	Kaplan-Meier Survival Analysis
BRCA	0.014	Kaplan-Meier Survival Analysis
KIRP	0.0039	Kaplan-Meier Survival Analysis
COAD	0.016	Kaplan-Meier Survival Analysis
CESC	0.004	Kaplan-Meier Survival Analysis
UCEC	0.0083	Kaplan-Meier Survival Analysis
GBM	0.041	Kaplan-Meier Survival Analysis
DLBC	0.049	Kaplan-Meier Survival Analysis
THCA	0.012	Kaplan-Meier Survival Analysis
UVM	0.048	Kaplan-Meier Survival Analysis

Drugs

Cell lines and drugs in GSE70138 or GSE92742

Description

RBPome

Expression

Transcripts

Gene Model

Phenotypes

PPI

Gene Ontology

Description

Ensembl ID: ENSG00000135723 (Gene tree)
Gene ID: 29109
Gene Symbol: FHOD1
Alias: FHOS
Full Name: formin homology 2 domain containing 1
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Minus strand
Length: 18,272 bases
Position: chr16:67,229,387-67,247,658
Accession: 17905
RBP type: non-canonical RBP
Summary: This gene encodes a protein which is a member of the formin/diaphanous family of proteins. The gene is ubiquitously expressed but is found in abundance in the spleen. The encoded protein has sequence homology to diaphanous and formin proteins within the Formin Homology (FH)1 and FH2 domains. It also contains a coiled-coil domain, a collagen-like domain, two nuclear localization signals, and several potential PKC and PKA phosphorylation sites. It is a predominantly cytoplasmic protein and is expressed in a variety of human cell lines. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]

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
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
ENST00000569085	FHOD1-209	735	-	-	- (aa)	-	-
ENST00000562266	FHOD1-203	486	-	-	- (aa)	-	-
ENST00000569888	FHOD1-210	780	-	-	- (aa)	-	-
ENST00000567509	FHOD1-205	563	-	ENSP00000462988	108 (aa)	-	J3KTH7
ENST00000566006	FHOD1-204	673	-	-	- (aa)	-	-
ENST00000567561	FHOD1-206	773	-	ENSP00000462807	22 (aa)	-	J3KT53
ENST00000568595	FHOD1-208	520	-	ENSP00000464011	28 (aa)	-	J3QR24
ENST00000258201	FHOD1-201	3990	XM_011523043	ENSP00000258201	1164 (aa)	XP_011521345	Q9Y613
ENST00000567752	FHOD1-207	4321	-	-	- (aa)	-	-
ENST00000561922	FHOD1-202	2069	-	ENSP00000458085	157 (aa)	-	H3BVE7

Gene Model

Click here to download ENSG00000135723's gene model file

Phenotypes

ensgID	Trait	pValue	Pubmed ID
ENSG00000135723	Cholesterol, HDL	9.713e-008	19060910
ENSG00000135723	Child Development Disorders, Pervasive	1.3191000E-005	-

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000135723's network

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

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0001725	stress fiber	15095401.	IDA	Component
GO:0003779	actin binding	-	IEA	Function
GO:0005515	protein binding	15095401.24880667.	IPI	Function
GO:0005634	nucleus	15095401.	IDA	Component
GO:0005737	cytoplasm	10352228.	TAS	Component
GO:0005829	cytosol	-	IDA	Component
GO:0007097	nuclear migration	-	IEA	Process
GO:0014704	intercalated disc	-	IEA	Component
GO:0016020	membrane	19946888.	HDA	Component
GO:0019904	protein domain specific binding	16361249.	IPI	Function
GO:0032059	bleb	-	IEA	Component
GO:0042802	identical protein binding	18239683.18786395.	IPI	Function
GO:0043621	protein self-association	16361249.	IMP	Function
GO:0045944	positive regulation of transcription by RNA polymerase II	15095401.	IDA	Process
GO:0045944	positive regulation of transcription by RNA polymerase II	16361249.	IMP	Process
GO:0051492	regulation of stress fiber assembly	16361249.	IMP	Process
GO:0051496	positive regulation of stress fiber assembly	15095401.	IDA	Process
GO:0051660	establishment of centrosome localization	-	IEA	Process

EuRBPDB

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Eesembl ID

Cell lines and drugs in GSE70138 or GSE92742

Description

RBPome

Expression

Transcripts

Gene Model

Phenotypes

PPI

Gene Ontology

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

Select Dataset :

Input Drug :

Input Cell Line :

Eesembl ID

Cell lines and drugs in GSE70138 or GSE92742

Note: to get the extension of tumor abbreviations.