EuRBPDB

Note: to get the extension of tumor abbreviations.

Cancer Related Information
Basic Information

Cancer associated literatures

PID	Title	Article	Time	Author	Doi
18581278	SMARCC1 expression is upregulated in prostate cancer and positively correlated with tumour recurrence and dedifferentiation.	Histol Histopathol	2008 Sep	Heebll S	doi: 10.14670/HH-23.1069.
23799850	miR-320c regulates gemcitabine-resistance in pancreatic cancer via SMARCC1.	Br J Cancer	2013 Jul 23	Iwagami Y	doi: 10.1038/bjc.2013.320
22139574	Identification of a core member of the SWI/SNF complex, BAF155/SMARCC1, as a human tumor suppressor gene.	Epigenetics	2011 Dec	DelBove J	doi: 10.4161/epi.6.12.18492.

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq
BLCA	chr3	47714447	Missense_Mutation	NA	E254K	0.33
BLCA	chr3	47710751	Missense_Mutation	NA	D284N	0.28
BLCA	chr3	47693248	Silent	novel	A406A	0.08
BLCA	chr3	47736036	Missense_Mutation	novel	Q192E	0.06
BLCA	chr3	47636041	Silent	NA	V824V	0.79
BLCA	chr3	47675513	Missense_Mutation	rs771918475	L601V	0.32
BLCA	chr3	47689422	Missense_Mutation	novel	E410K	0.61
BLCA	chr3	47661435	Missense_Mutation	novel	E727K	0.17
BLCA	chr3	47662566	Missense_Mutation	novel	W642C	0.25
BLCA	chr3	47662478	Missense_Mutation	novel	E672K	0.25
BLCA	chr3	47662406	Missense_Mutation	novel	M696V	0.22
BLCA	chr3	47635285	Missense_Mutation	NA	D851N	0.66
BRCA	chr3	47587755	3'UTR	novel		0.19
BRCA	chr3	47662469	Missense_Mutation	NA	D675N	0.3
BRCA	chr3	47635229	Silent	NA	A869A	0.48
BRCA	chr3	47686108	Silent	novel	V442V	0.33
BRCA	chr3	47587206	3'UTR	novel		0.67
BRCA	chr3	47587352	3'UTR	novel		0.71
BRCA	chr3	47638769	Missense_Mutation	NA	E778Q	0.21
BRCA	chr3	47680448	Missense_Mutation	novel	K482N	0.31
BRCA	chr3	47586910	3'UTR	novel		0.1
BRCA	chr3	47772859	Silent	novel	A91A	0.11
BRCA	chr3	47729062	Silent	novel	S203S	0.14
BRCA	chr3	47622338	Missense_Mutation	novel	L884M	0.07
BRCA	chr3	47678215	Silent	rs747800064	D518D	0.59
BRCA	chr3	47588130	3'UTR	novel		0.15
BRCA	chr3	47635330	Missense_Mutation	NA	E836K	0.19
BRCA	chr3	47661443	Missense_Mutation	rs746452222	R724Q	0.16
BRCA	chr3	47662386	Frame_Shift_Ins	NA	*L702Ffs34**	0.79
BRCA	chr3	47678208	Missense_Mutation	NA	A521S	0.12
BRCA	chr3	47588250	Missense_Mutation	novel	P1093A	0.14
CESC	chr3	47662506	Missense_Mutation	NA	L662F	0.37
CESC	chr3	47588094	3'UTR	novel		0.23
CESC	chr3	47706459	Silent	rs534717893	S330S	0.34
CESC	chr3	47588024	3'UTR	novel		0.6
CESC	chr3	47587728	3'UTR	novel		0.3
CESC	chr3	47670673	Silent	novel	T628T	0.28
CESC	chr3	47588107	3'UTR	novel		0.61
COAD	chr3	47714426	Missense_Mutation	novel	K261Q	0.31
COAD	chr3	47588183	3'UTR	rs767843750		0.32
COAD	chr3	47610123	Missense_Mutation	novel	P996S	0.27
COAD	chr3	47588114	3'UTR	novel		0.5
COAD	chr3	47588080	3'UTR	novel		0.38
COAD	chr3	47686070	Missense_Mutation	novel	A455V	0.25
COAD	chr3	47588149	3'UTR	novel		0.31
COAD	chr3	47636068	Frame_Shift_Ins	novel	*N815Kfs2**	0.32
COAD	chr3	47610249	Missense_Mutation	NA	A954T	0.37
COAD	chr3	47706519	Silent	novel	S310S	0.09
COAD	chr3	47590750	Missense_Mutation	NA	S1044F	0.19
ESCA	chr3	47706481	Missense_Mutation	rs769789233	R323Q	0.1
ESCA	chr3	47636072	Missense_Mutation	novel	K814R	0.45
ESCA	chr3	47586591	3'UTR	novel		0.16
GBM	chr3	47676772	Missense_Mutation	novel	F528V	0.12
GBM	chr3	47670681	Nonsense_Mutation	novel	Q626*	0.06
GBM	chr3	47686134	Missense_Mutation	novel	S434A	0.63
GBM	chr3	47729077	Missense_Mutation	novel	E198D	0.21
GBM	chr3	47714475	Silent	NA	V244V	0.1
HNSC	chr3	47662537	Missense_Mutation	novel	R652H	0.29
HNSC	chr3	47662381	Missense_Mutation	novel	S704F	0.27
KIRC	chr3	47636023	Splice_Region	NA	S830S	0.23
KIRC	chr3	47662570	Nonsense_Mutation	novel	*D641Gfs4**	0.08
KIRP	chr3	47638778	Missense_Mutation	novel	G775R	0.27
KIRP	chr3	47676682	Missense_Mutation	NA	V558L	0.14
LGG	chr3	47720694	Missense_Mutation	novel	L230V	0.13
LGG	chr3	47678297	Missense_Mutation	NA	R491Q	0.06
LGG	chr3	47588250	Missense_Mutation	novel	P1093T	0.35
LGG	chr3	47622323	Nonsense_Mutation	novel	E889*	0.37
LGG	chr3	47662426	Missense_Mutation	novel	S689N	0.3
LGG	chr3	47781615	Silent	novel	K61K	0.29
LIHC	chr3	47610239	Missense_Mutation	NA	Q957R	0.46
LUAD	chr3	47590776	Frame_Shift_Del	novel	*T1036Lfs26**	0.16
LUAD	chr3	47662420	Missense_Mutation	NA	S691L	0.4
LUAD	chr3	47622319	Missense_Mutation	NA	R890T	0.32
LUAD	chr3	47662571	Missense_Mutation	novel	D641N	0.12
LUAD	chr3	47636098	Missense_Mutation	NA	D805E	0.15
LUAD	chr3	47636100	Missense_Mutation	novel	D805Y	0.15
LUAD	chr3	47662441	Missense_Mutation	novel	Q684L	0.24
LUAD	chr3	47772869	Missense_Mutation	novel	Q88L	0.27
LUAD	chr3	47710773	Silent	NA	F276F	0.07
LUSC	chr3	47590732	Missense_Mutation	novel	P1050L	0.2
LUSC	chr3	47701335	Missense_Mutation	NA	D370Y	0.66
LUSC	chr3	47701277	Splice_Site	NA	X389_splice	0.56
LUSC	chr3	47729079	Missense_Mutation	novel	E198Q	0.36
LUSC	chr3	47662386	Frame_Shift_Ins	NA	*L702Ffs34**	0.19
LUSC	chr3	47662566	Missense_Mutation	NA	W642C	0.73
LUSC	chr3	47710773	Missense_Mutation	novel	F276L	0.56
LUSC	chr3	47661389	Missense_Mutation	rs768188371	Q742R	0.21
MESO	chr3	47782045	5'Flank	novel		0.26
OV	chr3	47693291	Frame_Shift_Ins	novel	*K392Ifs4**	0.11
OV	chr3	47693292	Nonsense_Mutation	novel	K392*	0.11
OV	chr3	47661372	Missense_Mutation	NA	S748P	0.61
PAAD	chr3	47610251	Missense_Mutation	rs769908274	R953Q	0.04
PAAD	chr3	47701313	Missense_Mutation	novel	V377A	0.18
PRAD	chr3	47622229	Missense_Mutation	novel	I920N	0.25
READ	chr3	47678274	Missense_Mutation	NA	R499C	0.25
READ	chr3	47706490	Missense_Mutation	novel	A320V	0.31
READ	chr3	47738081	Missense_Mutation	rs781064681	R144Q	0.24
SARC	chr3	47772913	Silent	novel	T73T	0.11
SKCM	chr3	47686124	Missense_Mutation	NA	L437R	0.27
SKCM	chr3	47706455	Missense_Mutation	rs746702299	P332S	0.36
SKCM	chr3	47661297	Missense_Mutation	NA	L773V	0.38
SKCM	chr3	47610119	Missense_Mutation	NA	P997L	0.09
SKCM	chr3	47662371	Silent	NA	D707D	0.22
SKCM	chr3	47676694	Missense_Mutation	NA	P554S	0.23
SKCM	chr3	47693267	Missense_Mutation	NA	V400G	0.71
SKCM	chr3	47675493	Silent	novel	S607S	0.19
SKCM	chr3	47590692	Silent	NA	P1063P	0.24
SKCM	chr3	47738077	Missense_Mutation	novel	M145I	0.28
SKCM	chr3	47714419	Nonsense_Mutation	NA	W263*	0.09
SKCM	chr3	47588160	3'UTR	novel		0.28
SKCM	chr3	47588161	3'UTR	novel		0.27
SKCM	chr3	47590816	Missense_Mutation	novel	S1022F	0.21
SKCM	chr3	47689400	Missense_Mutation	rs570224359	T417I	0.26
SKCM	chr3	47736071	Missense_Mutation	NA	L180S	0.36
SKCM	chr3	47772882	Missense_Mutation	NA	L84F	0.15
SKCM	chr3	47590777	Missense_Mutation	novel	P1035L	0.31
SKCM	chr3	47610077	Missense_Mutation	novel	P1011L	0.36
STAD	chr3	47678273	Missense_Mutation	rs759334676	R499H	0.16
STAD	chr3	47588275	Silent	NA	P1084P	0.47
STAD	chr3	47729087	Missense_Mutation	novel	F195C	0.64
STAD	chr3	47701358	Missense_Mutation	novel	D362V	0.18
STAD	chr3	47610252	Nonsense_Mutation	NA	R953*	0.06
STAD	chr3	47678297	Missense_Mutation	NA	R491Q	0.33
STAD	chr3	47675509	Missense_Mutation	NA	R602H	0.37
STAD	chr3	47636068	Frame_Shift_Ins	novel	*N815Kfs2**	0.4
STAD	chr3	47738072	Missense_Mutation	NA	R147H	0.22
STAD	chr3	47610292	Silent	NA	R939R	0.34
STAD	chr3	47689407	Missense_Mutation	rs776988969	T415A	0.17
STAD	chr3	47693290	Missense_Mutation	NA	K392N	0.27
STAD	chr3	47610294	Missense_Mutation	rs760989176	R939C	0.38
STAD	chr3	47636069	Frame_Shift_Del	NA	*N815Ifs10**	0.35
STAD	chr3	47745984	Missense_Mutation	NA	F109L	0.1
STAD	chr3	47689375	Splice_Site	novel	X421_splice	0.22
STAD	chr3	47590794	Missense_Mutation	novel	M1029I	0.67
STAD	chr3	47680457	Frame_Shift_Ins	novel	*N479Kfs18**	0.35
STAD	chr3	47610232	Silent	NA	E959E	0.19
STAD	chr3	47706446	Missense_Mutation	NA	T335A	0.16
STAD	chr3	47670688	Nonsense_Mutation	NA	W623*	0.23
UCEC	chr3	47587354	3'UTR	novel		0.14
UCEC	chr3	47635306	Missense_Mutation	NA	T844A	0.32
UCEC	chr3	47662476	Missense_Mutation	NA	E672D	0.15
UCEC	chr3	47676640	Nonsense_Mutation	NA	R572*	0.53
UCEC	chr3	47693286	Missense_Mutation	NA	D394Y	0.27
UCEC	chr3	47706460	Missense_Mutation	rs200399115	S330L	0.08
UCEC	chr3	47736041	Missense_Mutation	rs780153138	R190Q	0.54
UCEC	chr3	47587157	3'UTR	novel		0.3
UCEC	chr3	47587487	3'UTR	novel		0.32
UCEC	chr3	47693278	Silent	novel	E396E	0.42
UCEC	chr3	47706451	Frame_Shift_Del	novel	*P333Lfs35**	0.4
UCEC	chr3	47729083	Silent	rs561279574	T196T	0.44
UCEC	chr3	47662575	Silent	novel	K639K	0.29
UCEC	chr3	47586044	3'UTR	novel		0.33
UCEC	chr3	47638764	Missense_Mutation	novel	E779D	0.3
UCEC	chr3	47710705	Missense_Mutation	rs142093774	R299Q	0.08
UCEC	chr3	47678234	Missense_Mutation	NA	R512Q	0.35
UCEC	chr3	47710755	Nonsense_Mutation	novel	E283*	0.08
UCEC	chr3	47610226	Silent	NA	Q961Q	0.13
UCEC	chr3	47662494	Silent	novel	I666I	0.1
UCEC	chr3	47586044	3'UTR	novel		0.4
UCEC	chr3	47586044	3'UTR	novel		0.58
UCEC	chr3	47587232	3'UTR	novel		0.57
UCEC	chr3	47586852	3'UTR	novel		0.35
UCEC	chr3	47676697	Missense_Mutation	rs779079454	T553A	0.07
UCEC	chr3	47662378	Missense_Mutation	novel	V705A	0.34
UCEC	chr3	47706471	Silent	novel	K326K	0.39
UCEC	chr3	47738072	Missense_Mutation	NA	R147H	0.25
UCEC	chr3	47635249	Nonsense_Mutation	novel	E863*	0.31
UCEC	chr3	47662365	Silent	rs371760215	R709R	0.34
UCEC	chr3	47678257	Missense_Mutation	novel	E504D	0.35
UCEC	chr3	47587806	3'UTR	novel		0.4
UCEC	chr3	47675490	Missense_Mutation	novel	K608N	0.45
UCEC	chr3	47587097	3'UTR	rs115392384		0.33
UCEC	chr3	47706481	Missense_Mutation	rs769789233	R323Q	0.59
UCEC	chr3	47622229	Missense_Mutation	NA	I920S	0.35
UCEC	chr3	47586044	3'UTR	novel		0.43
UCEC	chr3	47662379	Missense_Mutation	novel	V705M	0.47
UCEC	chr3	47662342	Missense_Mutation	novel	A717V	0.09
UCEC	chr3	47686063	Missense_Mutation	NA	W457C	0.22
UCEC	chr3	47586044	3'UTR	novel		0.5
UCEC	chr3	47586044	3'UTR	novel		0.34
UCEC	chr3	47610228	In_Frame_Del	NA	L947_Q960del	0.17
UCEC	chr3	47586044	3'UTR	novel		0.38
UCEC	chr3	47586670	3'UTR	novel		0.13
UCEC	chr3	47590732	Missense_Mutation	novel	P1050L	0.26
UCEC	chr3	47714435	Missense_Mutation	NA	I258V	0.13
UCEC	chr3	47781676	Missense_Mutation	novel	K41T	0.5
UCEC	chr3	47586044	3'UTR	novel		0.43
UCEC	chr3	47661363	Frame_Shift_Ins	novel	*V751Sfs19**	0.3
UCEC	chr3	47662549	Missense_Mutation	novel	H648R	0.41
UCEC	chr3	47693269	Silent	NA	P399P	0.15
UCEC	chr3	47587129	3'UTR	novel		0.35
UCEC	chr3	47720736	Splice_Site	novel	X216_splice	0.39
UCEC	chr3	47586044	3'UTR	novel		0.93
UCEC	chr3	47736086	Missense_Mutation	novel	D175G	0.32
UCEC	chr3	47610246	Nonsense_Mutation	novel	R955*	0.54
UCEC	chr3	47610232	Silent	NA	E959E	0.46
UCEC	chr3	47678297	Missense_Mutation	NA	R491Q	0.2
UCEC	chr3	47587728	3'UTR	novel		0.19
UCEC	chr3	47610246	Nonsense_Mutation	novel	R955*	0.21
UCEC	chr3	47710692	Missense_Mutation	novel	K303N	0.12
UCEC	chr3	47720706	Nonsense_Mutation	novel	E226*	0.26
UCEC	chr3	47710682	Splice_Site	novel	X306_splice	0.45
UCEC	chr3	47588189	3'UTR	novel		0.3
UCEC	chr3	47610246	Nonsense_Mutation	novel	R955*	0.28
UCEC	chr3	47586043	3'UTR	rs200719659		0.41
UCEC	chr3	47586693	3'UTR	novel		0.23
UCEC	chr3	47610218	Missense_Mutation	novel	G964D	0.35
UCEC	chr3	47588110	3'UTR	novel		0.35
UCEC	chr3	47635318	Nonsense_Mutation	NA	E840*	0.27
UCEC	chr3	47710749	Missense_Mutation	NA	D284E	0.27
UCEC	chr3	47590668	Silent	rs202138987	N1071N	0.43
UCEC	chr3	47662537	Missense_Mutation	novel	R652H	0.21
UCEC	chr3	47701312	Silent	novel	V377V	0.22
UCEC	chr3	47587523	3'UTR	novel		0.33
UCEC	chr3	47586876	3'UTR	novel		0.33
UCEC	chr3	47622306	Silent	NA	S894S	0.26
UCEC	chr3	47610195	Nonsense_Mutation	novel	Q972*	0.27
UCEC	chr3	47586869	3'UTR	novel		0.41
UCEC	chr3	47588140	3'UTR	novel		0.44
UCEC	chr3	47662559	Missense_Mutation	novel	V645M	0.26
UCEC	chr3	47701310	Missense_Mutation	novel	P378L	0.4
UCEC	chr3	47670710	Missense_Mutation	NA	G616V	0.07
UVM	chr3	47588283	Missense_Mutation	novel	P1082T	0.09

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
CHOL	DEL	0.8056	0.02241
DLBC	DEL	0.1458	0.016959
GBM	DEL	0.0763	0.056565
LGG	DEL	0.0838	0.00089193
LUAD	DEL	0.343	0.0021265
PAAD	DEL	0.1902	0.030662
SARC	DEL	0.2062	0.0034746
SKCM	DEL	0.1635	0.13887
TGCT	DEL	0.2067	0.08422
THYM	DEL	0.0976	0.037527

Survival Analysis

Cancer	P-value	Q-value
THYM	0.0034	Kaplan-Meier Survival Analysis
KIRC	0.013	Kaplan-Meier Survival Analysis
SARC	0.00011	Kaplan-Meier Survival Analysis
MESO	0.0014	Kaplan-Meier Survival Analysis
ACC	0.00011	Kaplan-Meier Survival Analysis
SKCM	0.043	Kaplan-Meier Survival Analysis
PRAD	0.04	Kaplan-Meier Survival Analysis
COAD	0.046	Kaplan-Meier Survival Analysis
PAAD	0.035	Kaplan-Meier Survival Analysis
READ	0.0012	Kaplan-Meier Survival Analysis
LAML	0.0039	Kaplan-Meier Survival Analysis
KICH	0.027	Kaplan-Meier Survival Analysis
UCEC	0.018	Kaplan-Meier Survival Analysis
GBM	0.039	Kaplan-Meier Survival Analysis
LIHC	0.0014	Kaplan-Meier Survival Analysis
THCA	0.041	Kaplan-Meier Survival Analysis
UVM	0.00033	Kaplan-Meier Survival Analysis

Drugs

Cell lines and drugs in GSE70138 or GSE92742

Description

RBPome

Expression

Transcripts

Gene Model

Pathways

Phenotypes

GWAS

PPI

Gene Ontology

Description

Ensembl ID: ENSG00000173473 (Gene tree)
Gene ID: 6599
Gene Symbol: SMARCC1
Alias: BAF155|SRG3|Rsc8|CRACC1
Full Name: SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 1
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Minus strand
Length: 196,835 bases
Position: chr3:47,585,272-47,782,106
Accession: 11104
RBP type: non-canonical RBP
Summary: The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and contains a predicted leucine zipper motif typical of many transcription factors. [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
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
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
ENST00000485737	SMARCC1-206	631	-	-	- (aa)	-	-
ENST00000485833	SMARCC1-207	412	-	-	- (aa)	-	-
ENST00000254480	SMARCC1-201	6375	XM_011534034	ENSP00000254480	1105 (aa)	XP_011532336	Q92922
ENST00000454240	SMARCC1-203	636	-	ENSP00000414266	133 (aa)	-	F8WE13
ENST00000483847	SMARCC1-205	804	-	-	- (aa)	-	-
ENST00000492896	SMARCC1-208	568	-	-	- (aa)	-	-
ENST00000425518	SMARCC1-202	3827	-	-	- (aa)	-	-
ENST00000462198	SMARCC1-204	785	-	-	- (aa)	-	-

Gene Model

Click here to download ENSG00000173473's gene model file

Pathways

Pathway ID	Pathway Name	Source
hsa04714	Thermogenesis	KEGG
hsa05225	Hepatocellular carcinoma	KEGG

Phenotypes

ensgID	Trait	pValue	Pubmed ID
ENSG00000173473	Child Development Disorders, Pervasive	2.9660000E-005	-
ENSG00000173473	Child Development Disorders, Pervasive	8.1842000E-006	-

GWAS

ensgID	SNP	Chromosome	Position	SNP-risk	Trait	PubmedID	95% CI	Or or BEAT	EFO ID
ENSG00000173473	rs4858802	3	47599521	?	Body mass index	30595370			EFO_0004340
ENSG00000173473	rs62262084	3	47612332	T	Educational attainment (years of education)	30038396	[0.0094-0.016] unit decrease	0.0127	EFO_0004784
ENSG00000173473	rs13319205	3	47758726	A	Smoking initiation (ever regular vs never regular)	30643251	[0.011-0.022] unit increase	0.016539797	EFO_0006527

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000173473's network

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

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0000790	nuclear chromatin	16217013.	HDA	Component
GO:0000978	RNA polymerase II proximal promoter sequence-specific DNA binding	16217013.	HDA	Function
GO:0000980	RNA polymerase II distal enhancer sequence-specific DNA binding	16217013.	HDA	Function
GO:0000981	DNA-binding transcription factor activity, RNA polymerase II-specific	-	ISA	Function
GO:0001741	XY body	-	IEA	Component
GO:0003713	transcription coactivator activity	8804307.	NAS	Function
GO:0005515	protein binding	9891079.10078207.11238380.12368262.12917342.15985610.18303029.20111005.23540691.24421395.24434208.25416956.28420882.28533407.28753627.	IPI	Function
GO:0005634	nucleus	28753627.	IDA	Component
GO:0005654	nucleoplasm	-	IDA	Component
GO:0005654	nucleoplasm	-	TAS	Component
GO:0005737	cytoplasm	28753627.	IDA	Component
GO:0006337	nucleosome disassembly	8895581.	IDA	Process
GO:0006338	chromatin remodeling	10078207.11018012.11726552.	IDA	Process
GO:0006357	regulation of transcription by RNA polymerase II	8804307.	NAS	Process
GO:0007399	nervous system development	-	IEA	Process
GO:0008286	insulin receptor signaling pathway	-	IEA	Process
GO:0009887	animal organ morphogenesis	-	IEA	Process
GO:0016514	SWI/SNF complex	8804307.10078207.11078522.29374058.	IDA	Component
GO:0030850	prostate gland development	-	IEA	Process
GO:0031492	nucleosomal DNA binding	16217013.	HDA	Function
GO:0032435	negative regulation of proteasomal ubiquitin-dependent protein catabolic process	-	IEA	Process
GO:0032991	protein-containing complex	16217013.	HDA	Component
GO:0043044	ATP-dependent chromatin remodeling	16217013.	HDA	Process
GO:0045893	positive regulation of transcription, DNA-templated	11018012.	IDA	Process
GO:0045944	positive regulation of transcription by RNA polymerase II	-	IEA	Process
GO:0047485	protein N-terminus binding	12917342.	IPI	Function
GO:0071564	npBAF complex	-	ISS	Component
GO:0071565	nBAF complex	-	ISS	Component

EuRBPDB

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Cell lines and drugs in GSE70138 or GSE92742

Description

RBPome

Expression

Transcripts

Gene Model

Pathways

Phenotypes

GWAS

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.