EuRBPDB

Note: to get the extension of tumor abbreviations.

Cancer Related Information
Basic Information

Cancer associated literatures

PID	Title	Article	Time	Author	Doi
27352326	Association Between the LIG1 Polymorphisms and Lung Cancer Risk: A Meta-analysis of Case-Control Studies.	Cell Biochem Biophys	2015 Nov	Li D	doi: 10.1007/s12013-015-0619-3.
24084463	Human DNA ligase i (ligi) gene and risk of cervical cancer in North Indian women.	Exp Oncol	2013 Sep	Kaur S	-
26125914	Relationship between genetic polymorphisms of DNA ligase 1 and non-small cell lung cancer susceptibility and radiosensitivity.	Genet Mol Res	2015 Jun 26	Tian H	doi: 10.4238/2015.June.26.14.

Differential Expression

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq
BLCA	chr19	48137571	Missense_Mutation	NA	S402F	0.57
BLCA	chr19	48139993	Silent	rs763944587	L355L	0.18
BLCA	chr19	48157065	Missense_Mutation	NA	D107N	0.12
BLCA	chr19	48121007	Intron	novel		0.09
BLCA	chr19	48143914	Missense_Mutation	rs373988317	V276M	0.43
BLCA	chr19	48150085	Splice_Region	novel		0.13
BLCA	chr19	48127279	Missense_Mutation	novel	E668Q	0.43
BLCA	chr19	48139968	Splice_Region	novel		0.4
BLCA	chr19	48143892	Missense_Mutation	rs574879811	P283L	0.18
BRCA	chr19	48140059	Silent	NA	L333L	0.24
BRCA	chr19	48153970	Splice_Region	novel		0.34
BRCA	chr19	48117659	Missense_Mutation	NA	I854M	0.28
BRCA	chr19	48137724	Intron	NA		0.18
BRCA	chr19	48143575	Silent	novel	R294R	0.08
BRCA	chr19	48137534	Silent	NA	L414L	0.19
BRCA	chr19	48127994	Silent	NA	F616F	0.43
BRCA	chr19	48137666	Silent	NA	R370R	0.14
BRCA	chr19	48149788	Missense_Mutation	NA	P251A	0.44
CESC	chr19	48150124	Missense_Mutation	NA	P221S	0.22
CESC	chr19	48115671	Missense_Mutation	novel	S913C	0.33
CESC	chr19	48133012	Silent	rs189517194	C565C	0.22
CESC	chr19	48140085	Missense_Mutation	novel	P325S	0.15
CESC	chr19	48127942	Missense_Mutation	NA	P634S	0.44
CESC	chr19	48134065	Missense_Mutation	novel	E509K	0.49
CESC	chr19	48115929	Missense_Mutation	NA	R874W	0.49
CESC	chr19	48121243	Missense_Mutation	novel	R771Q	0.18
CESC	chr19	48134059	Missense_Mutation	novel	P511S	0.07
COAD	chr19	48140068	Silent	NA	V330V	0.43
COAD	chr19	48157138	Missense_Mutation	NA	K82N	0.37
COAD	chr19	48122967	Silent	rs142775724	Y733Y	0.16
COAD	chr19	48151368	Intron	novel		0.69
COAD	chr19	48153881	Missense_Mutation	NA	E153K	0.44
COAD	chr19	48137608	Nonsense_Mutation	NA	Q390*	0.13
COAD	chr19	48149822	Silent	NA	V239V	0.3
COAD	chr19	48131166	Silent	rs760499416	H577H	0.25
COAD	chr19	48150121	Missense_Mutation	rs750475498	R222C	0.31
COAD	chr19	48121265	Missense_Mutation	rs368406296	A764T	0.39
COAD	chr19	48140013	Missense_Mutation	rs3730947	V349M	0.34
COAD	chr19	48154049	Intron	novel		0.41
COAD	chr19	48121051	Intron	novel		0.19
COAD	chr19	48137687	Splice_Region	novel	G363G	0.18
COAD	chr19	48140126	Missense_Mutation	rs779134053	T311M	0.38
COAD	chr19	48161370	Splice_Site	novel	X81_splice	0.25
COAD	chr19	48135701	Missense_Mutation	novel	M501T	0.3
COAD	chr19	48133011	Missense_Mutation	rs121434560	E566K	0.28
COAD	chr19	48115920	Nonsense_Mutation	rs760305891	R877*	0.16
COAD	chr19	48153917	Missense_Mutation	NA	S141G	0.17
COAD	chr19	48151367	Intron	novel		0.29
COAD	chr19	48153916	Missense_Mutation	novel	S141N	0.35
COAD	chr19	48131154	Silent	rs745572723	G581G	0.25
COAD	chr19	48137738	Intron	novel		0.36
ESCA	chr19	48127301	Silent	rs774839059	F660F	0.51
GBM	chr19	48117703	Missense_Mutation	rs780457620	A840T	0.3
GBM	chr19	48122967	Silent	rs142775724	Y733Y	0.43
GBM	chr19	48127976	Silent	rs375967541	A622A	0.21
GBM	chr19	48133011	Missense_Mutation	rs121434560	E566K	0.44
GBM	chr19	48121129	Intron	novel		0.21
GBM	chr19	48165609	5'UTR	rs368100309		0.04
HNSC	chr19	48117709	Missense_Mutation	novel	P838S	0.28
HNSC	chr19	48151258	Missense_Mutation	rs564476088	T183M	0.23
HNSC	chr19	48153996	Intron	novel		0.27
HNSC	chr19	48121036	Intron	novel		0.2
HNSC	chr19	48143601	Splice_Site	novel	X286_splice	0.38
HNSC	chr19	48121000	Intron	novel		0.24
HNSC	chr19	48140109	Missense_Mutation	rs752805843	R317C	0.48
KIRC	chr19	48131142	Missense_Mutation	NA	K585N	0.18
KIRP	chr19	48121042	Intron	novel		0.53
LGG	chr19	48162262	Missense_Mutation	novel	K36T	0.37
LIHC	chr19	48153996	Intron	novel		0.14
LIHC	chr19	48140015	Missense_Mutation	novel	G348V	0.33
LIHC	chr19	48140016	Missense_Mutation	novel	G348C	0.31
LUAD	chr19	48161476	Missense_Mutation	NA	S47T	0.31
LUAD	chr19	48117725	Silent	rs373220034	P832P	0.33
LUAD	chr19	48117727	Missense_Mutation	novel	P832S	0.33
LUAD	chr19	48133062	Silent	novel	R549R	0.61
LUAD	chr19	48121126	Intron	novel		0.08
LUAD	chr19	48117674	Silent	NA	L849L	0.28
LUAD	chr19	48153999	Intron	novel		0.21
LUAD	chr19	48135735	Missense_Mutation	novel	E490K	0.1
LUAD	chr19	48127345	Missense_Mutation	NA	V646L	0.14
LUAD	chr19	48132995	Missense_Mutation	novel	G571V	0.55
LUAD	chr19	48120934	Intron	novel		0.29
LUAD	chr19	48137539	Missense_Mutation	NA	R413W	0.3
LUAD	chr19	48121155	Intron	novel		0.17
LUAD	chr19	48150105	Missense_Mutation	rs760552864	T227M	0.16
LUAD	chr19	48131165	Missense_Mutation	rs375683198	A578T	0.33
LUAD	chr19	48162281	Nonsense_Mutation	NA	E30*	0.07
LUAD	chr19	48151307	Missense_Mutation	novel	A167S	0.25
LUAD	chr19	48120985	Intron	novel		0.27
LUAD	chr19	48140001	Missense_Mutation	novel	V353F	0.52
LUAD	chr19	48150104	Silent	NA	T227T	0.52
LUAD	chr19	48149842	Splice_Site	NA	X233_splice	0.1
LUSC	chr19	48151292	Missense_Mutation	NA	E172Q	0.16
LUSC	chr19	48127973	Silent	novel	V623V	0.22
LUSC	chr19	48115929	Missense_Mutation	NA	R874W	0.09
LUSC	chr19	48161460	Missense_Mutation	rs4987181	P52L	0.23
LUSC	chr19	48127922	Silent	novel	T640T	0.2
LUSC	chr19	48133012	Missense_Mutation	NA	C565W	0.44
LUSC	chr19	48151358	Intron	novel		0.27
LUSC	chr19	48121114	Intron	novel		0.39
LUSC	chr19	48133038	Missense_Mutation	rs372831646	R557C	0.23
LUSC	chr19	48140139	Missense_Mutation	novel	R307G	0.18
LUSC	chr19	48121183	Missense_Mutation	novel	Q791L	0.23
OV	chr19	48121067	Intron	novel		0.08
OV	chr19	48151328	Missense_Mutation	NA	P160A	0.57
OV	chr19	48133042	Silent	novel	L555L	0.04
OV	chr19	48128003	Frame_Shift_Ins	novel	*T614Ifs112**	0.04
OV	chr19	48135721	Silent	rs753665588	T494T	0.2
PAAD	chr19	48151258	Missense_Mutation	rs564476088	T183M	0.06
PCPG	chr19	48117745	Missense_Mutation	novel	I826L	0.29
PCPG	chr19	48143896	Missense_Mutation	novel	K282E	0.4
PRAD	chr19	48151282	Missense_Mutation	NA	G175E	0.22
PRAD	chr19	48117724	Missense_Mutation	rs747656528	D833N	0.26
PRAD	chr19	48122960	Missense_Mutation	rs755197772	A736T	0.23
READ	chr19	48117775	Missense_Mutation	NA	V816M	0.29
READ	chr19	48157027	Silent	rs111516401	P119P	0.41
SKCM	chr19	48137080	Missense_Mutation	novel	T420I	0.44
SKCM	chr19	48115920	Nonsense_Mutation	rs760305891	R877*	0.36
SKCM	chr19	48137662	Missense_Mutation	NA	E372K	0.08
SKCM	chr19	48127931	Silent	NA	V637V	0.36
SKCM	chr19	48151244	Silent	novel	L188L	0.22
SKCM	chr19	48151245	Silent	rs779397848	P187P	0.22
SKCM	chr19	48153961	Missense_Mutation	NA	K126T	0.2
SKCM	chr19	48150123	Missense_Mutation	NA	P221L	0.19
SKCM	chr19	48137673	Missense_Mutation	novel	S368F	0.44
SKCM	chr19	48115716	Missense_Mutation	rs752573864	R898Q	0.18
SKCM	chr19	48121069	Intron	novel		0.15
SKCM	chr19	48135779	Missense_Mutation	NA	E475V	0.22
SKCM	chr19	48117757	Missense_Mutation	NA	P822S	0.19
SKCM	chr19	48115913	Missense_Mutation	NA	R879P	0.21
SKCM	chr19	48161461	Missense_Mutation	NA	P52S	0.1
SKCM	chr19	48115627	3'UTR	novel		0.14
SKCM	chr19	48121086	Intron	novel		0.16
SKCM	chr19	48153929	Silent	NA	L137L	0.53
SKCM	chr19	48162271	Missense_Mutation	novel	P33L	0.51
SKCM	chr19	48139981	Silent	NA	A359A	0.12
SKCM	chr19	48143574	Missense_Mutation	NA	T295A	0.14
SKCM	chr19	48143576	Missense_Mutation	rs762145736	R294Q	0.15
SKCM	chr19	48157093	Silent	NA	T97T	0.15
SKCM	chr19	48157105	Silent	NA	P93P	0.3
SKCM	chr19	48117671	Silent	novel	S850S	0.24
SKCM	chr19	48117672	Missense_Mutation	novel	S850F	0.2
SKCM	chr19	48137672	Silent	rs765788847	S368S	0.27
SKCM	chr19	48140090	Missense_Mutation	rs760367725	S323L	0.22
SKCM	chr19	48140105	Missense_Mutation	rs111507847	S318F	0.36
STAD	chr19	48157022	Missense_Mutation	rs377155700	R121H	0.16
STAD	chr19	48117704	Silent	rs761804615	S839S	0.33
STAD	chr19	48127963	Missense_Mutation	rs762816837	R627W	0.4
STAD	chr19	48135732	Missense_Mutation	NA	A491T	0.36
STAD	chr19	48121230	Silent	rs556985324	Y775Y	0.28
STAD	chr19	48151368	Intron	novel		0.17
STAD	chr19	48115695	Missense_Mutation	novel	N905S	0.22
STAD	chr19	48133012	Silent	rs189517194	C565C	0.4
STAD	chr19	48150104	Silent	rs201868704	T227T	0.11
STAD	chr19	48151330	Missense_Mutation	NA	T159N	0.36
STAD	chr19	48121276	Missense_Mutation	NA	V760A	0.17
STAD	chr19	48157108	Silent	rs761326605	P92P	0.47
STAD	chr19	48121013	Intron	novel		0.26
STAD	chr19	48153946	Missense_Mutation	rs368320718	R131Q	0.22
STAD	chr19	48137549	Silent	rs142732689	R409R	0.27
STAD	chr19	48123211	Silent	rs769895197	I704I	0.26
STAD	chr19	48133038	Missense_Mutation	rs372831646	R557C	0.28
STAD	chr19	48143553	Missense_Mutation	NA	V302M	0.29
UCEC	chr19	48123288	Missense_Mutation	rs531348489	R679W	0.43
UCEC	chr19	48115898	Missense_Mutation	rs201176712	P884L	0.36
UCEC	chr19	48127955	Missense_Mutation	NA	K629N	0.36
UCEC	chr19	48120972	Intron	novel		0.3
UCEC	chr19	48121237	Missense_Mutation	novel	G773D	0.17
UCEC	chr19	48127981	Missense_Mutation	NA	E621K	0.33
UCEC	chr19	48133072	Silent	novel	A545A	0.43
UCEC	chr19	48137029	Nonsense_Mutation	NA	S437*	0.35
UCEC	chr19	48132987	Missense_Mutation	novel	A574T	0.42
UCEC	chr19	48117780	Missense_Mutation	novel	A814V	0.15
UCEC	chr19	48115510	3'UTR	novel		0.73
UCEC	chr19	48137078	Missense_Mutation	NA	A421S	0.46
UCEC	chr19	48122975	Missense_Mutation	NA	A731T	0.28
UCEC	chr19	48150209	Missense_Mutation	NA	K192N	0.31
UCEC	chr19	48115682	Silent	rs41546017	E909E	0.4
UCEC	chr19	48137644	Missense_Mutation	novel	D378N	0.34
UCEC	chr19	48161430	Missense_Mutation	novel	R62Q	0.31
UCEC	chr19	48131165	Missense_Mutation	rs375683198	A578T	0.47
UCEC	chr19	48123201	Missense_Mutation	rs140087554	A708T	0.22
UCEC	chr19	48150202	Missense_Mutation	novel	T195A	0.07
UCEC	chr19	48150203	Missense_Mutation	NA	E194D	0.22
UCEC	chr19	48151344	Splice_Region	novel		0.08
UCEC	chr19	48150104	Silent	rs201868704	T227T	0.36
UCEC	chr19	48151302	Missense_Mutation	NA	E168D	0.36
UCEC	chr19	48121030	Intron	novel		0.25
UCEC	chr19	48123212	Missense_Mutation	novel	I704T	0.39
UCEC	chr19	48117736	Missense_Mutation	rs770718097	A829T	0.5
UCEC	chr19	48149835	Frame_Shift_Ins	novel	*R235Pfs24**	0.27
UCEC	chr19	48143930	Missense_Mutation	novel	K270N	0.65
UCEC	chr19	48120929	Intron	novel		0.43
UCEC	chr19	48121295	Missense_Mutation	novel	G754S	0.56
UCEC	chr19	48153944	Missense_Mutation	NA	T132A	0.52
UCEC	chr19	48140138	Missense_Mutation	NA	R307Q	0.45
UCEC	chr19	48115510	3'UTR	novel		0.4
UCEC	chr19	48120948	Intron	novel		0.33
UCEC	chr19	48115558	3'UTR	novel		0.31
UCEC	chr19	48137689	Splice_Site	novel	X363_splice	0.28
UCEC	chr19	48161503	Missense_Mutation	novel	A38T	0.35
UCEC	chr19	48149836	Frame_Shift_Del	NA	*R235Gfs9**	0.54
UCEC	chr19	48150203	Missense_Mutation	NA	E194D	0.19
UCEC	chr19	48117664	Missense_Mutation	novel	P853S	0.4
UCEC	chr19	48149815	Nonsense_Mutation	novel	E242*	0.25
UCEC	chr19	48137013	Silent	novel	I442I	0.23
UCEC	chr19	48127300	Missense_Mutation	rs753568865	D661N	0.53
UCEC	chr19	48121203	Silent	NA	D784D	0.37
UCEC	chr19	48123271	Missense_Mutation	NA	E684D	0.44
UCEC	chr19	48121004	Intron	novel		0.17
UCEC	chr19	48115479	3'UTR	novel		0.45
UCEC	chr19	48119180	Missense_Mutation	novel	G799D	0.32
UCEC	chr19	48121225	Missense_Mutation	rs761317989	G777D	0.18
UCEC	chr19	48115567	3'UTR	novel		0.47
UCEC	chr19	48117700	Missense_Mutation	novel	V841M	0.45
UCEC	chr19	48143950	Missense_Mutation	novel	S264P	0.38
UCEC	chr19	48121007	Intron	novel		0.17
UCEC	chr19	48127990	Missense_Mutation	novel	L618M	0.11
UCEC	chr19	48151298	Missense_Mutation	NA	A170T	0.5
UCEC	chr19	48133037	Missense_Mutation	rs746737248	R557H	0.21
UCEC	chr19	48117752	Silent	rs761859667	Y823Y	0.27
UCEC	chr19	48135724	Silent	NA	K493K	0.13
UCEC	chr19	48115667	Silent	novel	D914D	0.15
UCEC	chr19	48157019	Missense_Mutation	rs368094694	R122H	0.45
UCEC	chr19	48157045	Silent	novel	S113S	0.44
UCEC	chr19	48121238	Missense_Mutation	rs751418904	G773S	0.27
UCEC	chr19	48137616	Missense_Mutation	rs777331327	R387H	0.38
UCEC	chr19	48133011	Missense_Mutation	rs121434560	E566K	0.29
UCS	chr19	48120972	Intron	novel		0.39

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
CESC	DEL	0.0949	0.027508
KIRP	DEL	0.0486	0.054726
LUAD	DEL	0.2578	1.5526e-05
LUSC	DEL	0.2136	1.1877e-06
OV	DEL	0.4784	2.441e-17
PAAD	DEL	0.087	0.035089
READ	DEL	0.0909	0.23023
TGCT	DEL	0.2867	0.0046229
UCS	DEL	0.2321	0.12448

Survival Analysis

Cancer	P-value	Q-value
THYM	0.0047	Kaplan-Meier Survival Analysis
KIRC	0.011	Kaplan-Meier Survival Analysis
STAD	0.046	Kaplan-Meier Survival Analysis
SARC	0.0039	Kaplan-Meier Survival Analysis
MESO	0.00012	Kaplan-Meier Survival Analysis
ACC	0.00014	Kaplan-Meier Survival Analysis
HNSC	0.02	Kaplan-Meier Survival Analysis
SKCM	0.001	Kaplan-Meier Survival Analysis
PRAD	0.0034	Kaplan-Meier Survival Analysis
PCPG	0.048	Kaplan-Meier Survival Analysis
BLCA	0.023	Kaplan-Meier Survival Analysis
CESC	0.00049	Kaplan-Meier Survival Analysis
READ	0.018	Kaplan-Meier Survival Analysis
KICH	0.022	Kaplan-Meier Survival Analysis
LIHC	0.011	Kaplan-Meier Survival Analysis
THCA	0.047	Kaplan-Meier Survival Analysis
LUAD	0.05	Kaplan-Meier Survival Analysis
UVM	0.03	Kaplan-Meier Survival Analysis

Drugs

Cell lines and drugs in GSE70138 or GSE92742

Description

RBPome

Expression

Transcripts

Gene Model

Pathways

Phenotypes

PPI

Gene Ontology

Description

Ensembl ID: ENSG00000105486 (Gene tree)
Gene ID: 3978
Gene Symbol: LIG1
Alias: N
Full Name: DNA ligase 1
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Minus strand
Length: 55,160 bases
Position: chr19:48,115,444-48,170,603
Accession: 6598
RBP type: non-canonical RBP
Summary: This gene encodes a member of the ATP-dependent DNA ligase protein family. The encoded protein functions in DNA replication, recombination, and the base excision repair process. Mutations in this gene that lead to DNA ligase I deficiency result in immunodeficiency and increased sensitivity to DNA-damaging agents. Disruption of this gene may also be associated with a variety of cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]

RNA binding proteome (RBPome)

PID	Title	Method	Time	Author	Doi
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

Expression

Transcripts

Transcript ID	Name	Length	RefSeq ID	Protein ID	Length	RefSeq ID	UniportKB ID
ENST00000542460	LIG1-204	1527	-	ENSP00000445928	415 (aa)	-	B4E135
ENST00000595758	LIG1-208	606	-	-	- (aa)	-	-
ENST00000596457	LIG1-211	792	-	-	- (aa)	-	-
ENST00000536218	LIG1-203	3179	-	ENSP00000441531	851 (aa)	-	F5GZ28
ENST00000427526	LIG1-202	3027	-	ENSP00000442841	888 (aa)	-	P18858
ENST00000596104	LIG1-209	531	-	-	- (aa)	-	-
ENST00000593425	LIG1-205	575	-	ENSP00000469638	145 (aa)	-	M0QY71
ENST00000594759	LIG1-207	4102	-	ENSP00000471380	800 (aa)	-	M0R0Q7
ENST00000599322	LIG1-218	620	-	-	- (aa)	-	-
ENST00000600055	LIG1-219	602	-	-	- (aa)	-	-
ENST00000597901	LIG1-215	565	-	-	- (aa)	-	-
ENST00000598938	LIG1-216	377	-	ENSP00000472085	28 (aa)	-	M0R1S4
ENST00000263274	LIG1-201	3384	XM_024451513	ENSP00000263274	919 (aa)	XP_024307281	P18858
ENST00000597146	LIG1-214	589	-	-	- (aa)	-	-
ENST00000601091	LIG1-220	3957	-	ENSP00000471836	801 (aa)	-	P18858
ENST00000599165	LIG1-217	570	-	-	- (aa)	-	-
ENST00000596672	LIG1-213	792	-	ENSP00000472331	36 (aa)	-	M0R254
ENST00000596332	LIG1-210	584	-	-	- (aa)	-	-
ENST00000594067	LIG1-206	2697	-	-	- (aa)	-	-
ENST00000613670	LIG1-221	3949	-	ENSP00000483027	801 (aa)	-	P18858
ENST00000596549	LIG1-212	580	-	ENSP00000471861	149 (aa)	-	M0R1G7

Gene Model

Click here to download ENSG00000105486's gene model file

Pathways

Pathway ID	Pathway Name	Source
hsa03030	DNA replication	KEGG
hsa03410	Base excision repair	KEGG
hsa03420	Nucleotide excision repair	KEGG
hsa03430	Mismatch repair	KEGG

Phenotypes

ensgID	Trait	pValue	Pubmed ID
ENSG00000105486	Platelet Function Tests	1.1009500E-005	-
ENSG00000105486	Platelet Function Tests	1.1009500E-005	-

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000105486's network

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

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0003677	DNA binding	-	IEA	Function
GO:0003909	DNA ligase activity	9809069.	IDA	Function
GO:0003909	DNA ligase activity	15871698.	IMP	Function
GO:0003909	DNA ligase activity	-	TAS	Function
GO:0003910	DNA ligase (ATP) activity	21873635.	IBA	Function
GO:0005524	ATP binding	-	IEA	Function
GO:0005634	nucleus	21873635.	IBA	Component
GO:0005654	nucleoplasm	-	IDA	Component
GO:0005654	nucleoplasm	-	TAS	Component
GO:0005737	cytoplasm	21873635.	IBA	Component
GO:0005739	mitochondrion	21873635.	IBA	Component
GO:0006266	DNA ligation	-	TAS	Process
GO:0006273	lagging strand elongation	21873635.	IBA	Process
GO:0006281	DNA repair	8696349.	TAS	Process
GO:0006283	transcription-coupled nucleotide-excision repair	-	TAS	Process
GO:0006284	base-excision repair	19589734.	IDA	Process
GO:0006297	nucleotide-excision repair, DNA gap filling	-	TAS	Process
GO:0006298	mismatch repair	-	TAS	Process
GO:0009653	anatomical structure morphogenesis	8696349.	TAS	Process
GO:0033151	V(D)J recombination	9809069.	IDA	Process
GO:0043231	intracellular membrane-bounded organelle	-	IDA	Component
GO:0046872	metal ion binding	-	IEA	Function
GO:0051103	DNA ligation involved in DNA repair	-	IEA	Process
GO:0051301	cell division	-	IEA	Process
GO:0071897	DNA biosynthetic process	-	IEA	Process
GO:1903461	Okazaki fragment processing involved in mitotic DNA replication	21873635.	IBA	Process

EuRBPDB

Note: to get the extension of tumor abbreviations.

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Input Drug :

Input Cell Line :

Eesembl ID

Cell lines and drugs in GSE70138 or GSE92742

Description

RBPome

Expression

Transcripts

Gene Model

Pathways

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.