EuRBPDB

Note: to get the extension of tumor abbreviations.

Cancer Related Information
Basic Information

Differential Expression

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq	RBD
ACC	chr19	17772469	Missense_Mutation	novel	M203V	0.48
BLCA	chr19	17784865	Missense_Mutation	novel	Q789H	0.3
BLCA	chr19	17766685	In_Frame_Del	novel	W71_E72del	0.36
BLCA	chr19	17762765	Missense_Mutation	novel	E11K	0.08
BLCA	chr19	17784743	Missense_Mutation	NA	Q749E	0.25
BLCA	chr19	17775485	Silent	novel	F325F	0.27
BLCA	chr19	17766681	Silent	rs780435067	P69P	0.52
BLCA	chr19	17778612	Missense_Mutation	NA	S452F	0.6
BLCA	chr19	17770481	Missense_Mutation	novel	S131R	0.28	U1snRNP70_N
BLCA	chr19	17770543	Missense_Mutation	rs770292906	R152Q	0.51	U1snRNP70_N
BLCA	chr19	17781804	Missense_Mutation	rs534109677	R641C	0.6
BLCA	chr19	17781722	Silent	NA	R613R	0.83
BLCA	chr19	17786584	Missense_Mutation	NA	E813K	0.4
BLCA	chr19	17772651	Missense_Mutation	NA	E234K	0.13
BLCA	chr19	17764385	Missense_Mutation	novel	E44K	0.21
BLCA	chr19	17770568	Missense_Mutation	novel	E160D	0.24	U1snRNP70_N
BLCA	chr19	17781817	Missense_Mutation	novel	P645L	0.27
BRCA	chr19	17778144	Missense_Mutation	NA	E423Q	0.16
BRCA	chr19	17776259	Missense_Mutation	NA	R399C	0.29
BRCA	chr19	17772463	Nonsense_Mutation	NA	Q201*	0.44
BRCA	chr19	17786574	Nonsense_Mutation	novel	W809*	0.05
BRCA	chr19	17784809	Missense_Mutation	NA	E771K	0.86
BRCA	chr19	17778643	Silent	NA	S462S	0.6
BRCA	chr19	17764390	Missense_Mutation	rs747956233	E45D	0.13
CESC	chr19	17774445	Missense_Mutation	rs530821806	R296Q	0.46
CESC	chr19	17762803	Silent	novel	V23V	0.33
COAD	chr19	17766702	Silent	NA	V76V	0.33
COAD	chr19	17778207	Missense_Mutation	novel	F444L	0.06
COAD	chr19	17774408	Missense_Mutation	rs142820853	R284W	0.16
COAD	chr19	17776248	Missense_Mutation	novel	G395D	0.4
COAD	chr19	17772537	Silent	rs779991590	T225T	0.25
COAD	chr19	17784224	Silent	novel	L739L	0.41
COAD	chr19	17774237	Splice_Site	novel	X264_splice	0.23
COAD	chr19	17783155	Silent	rs747446709	N692N	0.36
COAD	chr19	17770542	Missense_Mutation	novel	R152W	0.32	U1snRNP70_N
COAD	chr19	17772537	Silent	rs779991590	T225T	0.28
COAD	chr19	17781769	Missense_Mutation	novel	A629V	0.09
COAD	chr19	17770793	Missense_Mutation	rs144793428	A164V	0.18	U1snRNP70_N
COAD	chr19	17784732	Missense_Mutation	rs151277101	R745H	0.34
COAD	chr19	17788401	3'UTR	novel		0.36
COAD	chr19	17772714	Missense_Mutation	NA	S255R	0.11
COAD	chr19	17778769	Silent	novel	S504S	0.27
COAD	chr19	17772534	Missense_Mutation	novel	D224E	0.07
COAD	chr19	17784813	Missense_Mutation	novel	Y772C	0.27
COAD	chr19	17764404	Missense_Mutation	NA	A50V	0.36
COAD	chr19	17788340	3'UTR	rs192038426		0.39
COAD	chr19	17766753	Missense_Mutation	NA	Q93H	0.16
DLBC	chr19	17786619	Silent	rs370950809	S824S	0.76
ESCA	chr19	17788475	3'UTR	rs552257817		0.16
ESCA	chr19	17755130	5'UTR	rs374696612		0.16
ESCA	chr19	17766707	Missense_Mutation	novel	S78L	0.26
GBM	chr19	17766791	Missense_Mutation	novel	Q106R	0.12	U1snRNP70_N
GBM	chr19	17781776	Silent	novel	A631A	0.13
GBM	chr19	17783021	Missense_Mutation	novel	L648M	0.14
GBM	chr19	17766686	Frame_Shift_Ins	novel	*W71Cfs19**	0.48
GBM	chr19	17787765	Missense_Mutation	novel	G856R	0.16
GBM	chr19	17784852	Missense_Mutation	novel	L785H	0.17
HNSC	chr19	17781503	Missense_Mutation	novel	L598M	0.21
HNSC	chr19	17764411	Silent	rs148025294	A52A	0.16
HNSC	chr19	17776673	Missense_Mutation	rs760083911	P416A	0.22
HNSC	chr19	17766759	Silent	novel	L95L	0.59
HNSC	chr19	17784825	Missense_Mutation	rs747467663	P776L	0.26
HNSC	chr19	17776079	Missense_Mutation	rs751850968	R367L	0.44
HNSC	chr19	17781467	Missense_Mutation	novel	P586S	0.64
KIRC	chr19	17755142	5'UTR	novel		0.18
KIRP	chr19	17788434	3'UTR	novel		0.4
KIRP	chr19	17770526	Missense_Mutation	novel	M146I	0.39	U1snRNP70_N
LGG	chr19	17775468	Missense_Mutation	NA	V320M	0.1
LGG	chr19	17778191	Silent	novel	P438P	0.38
LGG	chr19	17784880	Silent	NA	V794V	0.14
LIHC	chr19	17776117	Missense_Mutation	NA	L380I	0.94
LIHC	chr19	17772695	Silent	novel	L248L	0.35
LIHC	chr19	17788529	3'UTR	novel		0.41
LIHC	chr19	17766713	Missense_Mutation	novel	K80T	0.18
LUAD	chr19	17772477	Silent	NA	E205E	0.12
LUAD	chr19	17766811	Splice_Site	novel	X112_splice	0.59
LUAD	chr19	17783057	Missense_Mutation	NA	P660T	0.73
LUAD	chr19	17784926	Splice_Site	NA	X809_splice	0.39
LUAD	chr19	17784804	Nonsense_Mutation	novel	S769*	0.17
LUAD	chr19	17755152	5'UTR	novel		0.56
LUAD	chr19	17781238	Missense_Mutation	NA	M545I	0.08
LUAD	chr19	17783157	Missense_Mutation	NA	A693D	0.45
LUAD	chr19	17774421	Missense_Mutation	NA	A288D	0.45
LUAD	chr19	17781718	Missense_Mutation	rs747334107	S612Y	0.19
LUAD	chr19	17781719	Silent	novel	S612S	0.19
LUAD	chr19	17776040	Missense_Mutation	novel	P354H	0.44
LUSC	chr19	17774426	Missense_Mutation	novel	R290G	0.38
LUSC	chr19	17783085	Missense_Mutation	NA	G669E	0.15
LUSC	chr19	17776089	Silent	novel	A370A	0.35
LUSC	chr19	17770885	Missense_Mutation	NA	D195Y	0.21
LUSC	chr19	17788411	3'UTR	novel		0.56
LUSC	chr19	17776101	Frame_Shift_Del	novel	*A375Qfs23**	0.37
LUSC	chr19	17764380	Missense_Mutation	NA	T42N	0.25
LUSC	chr19	17775078	Missense_Mutation	novel	G315W	0.37
LUSC	chr19	17775079	Missense_Mutation	novel	G315V	0.37
LUSC	chr19	17762734	Intron	novel		0.08
LUSC	chr19	17784783	Missense_Mutation	NA	G762A	0.06
LUSC	chr19	17783130	Missense_Mutation	novel	T684I	0.26
LUSC	chr19	17766769	Missense_Mutation	novel	V99F	0.25
LUSC	chr19	17788311	3'UTR	novel		0.24
LUSC	chr19	17776036	Missense_Mutation	novel	E353K	0.26
MESO	chr19	17781795	Missense_Mutation	rs746424375	A638T	0.66
OV	chr19	17781722	Silent	novel	R613R	0.06
OV	chr19	17784169	Silent	novel	A720A	0.34
OV	chr19	17787794	Silent	novel	E865E	0.09
OV	chr19	17770876	Missense_Mutation	novel	K192E	0.06
OV	chr19	17784217	Frame_Shift_Del	novel	*V737Cfs62**	0.38
OV	chr19	17755150	5'UTR	novel		0.13
PAAD	chr19	17762830	Silent	novel	E32E	0.16
PAAD	chr19	17784224	Missense_Mutation	novel	L739M	0.25
PRAD	chr19	17755144	5'UTR	novel		0.21
PRAD	chr19	17766716	Missense_Mutation	novel	L81P	0.43
PRAD	chr19	17783156	Missense_Mutation	rs761157532	A693T	0.33
READ	chr19	17787820	Missense_Mutation	NA	S874L	0.35
READ	chr19	17770863	Silent	novel	A187A	0.33
SARC	chr19	17770519	Missense_Mutation	rs767793852	R144H	0.29	U1snRNP70_N
SARC	chr19	17766626	Intron	novel		0.3
SARC	chr19	17770542	Missense_Mutation	novel	R152W	0.14	U1snRNP70_N
SARC	chr19	17776021	Missense_Mutation	rs781383645	D348N	0.12
SKCM	chr19	17786603	Missense_Mutation	novel	R819K	0.3
SKCM	chr19	17755164	5'UTR	novel		0.36
SKCM	chr19	17770562	Silent	NA	Q158Q	0.45
SKCM	chr19	17766797	Missense_Mutation	NA	K108T	0.32	U1snRNP70_N
SKCM	chr19	17784863	Nonsense_Mutation	novel	Q789*	0.26
SKCM	chr19	17781455	Missense_Mutation	rs768328075	R582C	0.27
SKCM	chr19	17781526	Silent	novel	S605S	0.14
SKCM	chr19	17778855	Missense_Mutation	NA	P533L	0.35
SKCM	chr19	17784880	Silent	NA	V794V	0.37
SKCM	chr19	17783028	Missense_Mutation	rs150758103	R650Q	0.43
SKCM	chr19	17784883	Silent	novel	G795G	0.38
SKCM	chr19	17776138	Missense_Mutation	NA	L387F	0.07
SKCM	chr19	17781804	Missense_Mutation	rs534109677	R641C	0.36
SKCM	chr19	17784228	Missense_Mutation	rs374251080	R740Q	0.27
SKCM	chr19	17781727	Missense_Mutation	rs746345884	P615L	0.07
SKCM	chr19	17755170	Silent	rs148890860	S2S	0.29
SKCM	chr19	17764411	Silent	rs148025294	A52A	0.16
SKCM	chr19	17775991	Missense_Mutation	rs374706299	E338K	0.15
SKCM	chr19	17774253	Missense_Mutation	rs770875917	E269K	0.26
SKCM	chr19	17788372	3'UTR	novel		0.25
SKCM	chr19	17775988	Missense_Mutation	NA	A337T	0.3
SKCM	chr19	17766795	Silent	novel	L107L	0.32
SKCM	chr19	17784194	Missense_Mutation	novel	P729S	0.7
SKCM	chr19	17784195	Missense_Mutation	novel	P729L	0.7
SKCM	chr19	17774436	Missense_Mutation	novel	G293E	0.25
SKCM	chr19	17770498	Missense_Mutation	NA	S137F	0.38	U1snRNP70_N
SKCM	chr19	17781726	Missense_Mutation	NA	P615S	0.5
SKCM	chr19	17781533	Missense_Mutation	NA	G608R	0.4
SKCM	chr19	17764384	Silent	novel	I43I	0.38
SKCM	chr19	17766766	Missense_Mutation	novel	D98N	0.23
SKCM	chr19	17764398	Missense_Mutation	novel	S48L	0.24
SKCM	chr19	17774455	Silent	novel	R299R	0.45
STAD	chr19	17774427	Missense_Mutation	rs141405200	R290H	0.38
STAD	chr19	17772688	Missense_Mutation	NA	E246G	0.11
STAD	chr19	17772524	Missense_Mutation	rs531090742	S221L	0.15
STAD	chr19	17770571	Missense_Mutation	novel	M161I	0.15	U1snRNP70_N
STAD	chr19	17783083	Silent	rs767033905	S668S	0.1
STAD	chr19	17772541	Missense_Mutation	novel	V227M	0.35
STAD	chr19	17783083	Silent	rs767033905	S668S	0.34
STAD	chr19	17784189	Missense_Mutation	novel	Q727R	0.3
STAD	chr19	17772537	Silent	NA	T225T	0.49
STAD	chr19	17783084	Missense_Mutation	rs750801082	G669R	0.1
STAD	chr19	17775982	Splice_Site	rs772008992	X335_splice	0.37
STAD	chr19	17776670	Frame_Shift_Ins	novel	*R417Qfs29**	0.29
STAD	chr19	17775982	Splice_Site	rs772008992	X335_splice	0.23
STAD	chr19	17766811	Splice_Site	novel	X112_splice	0.33
STAD	chr19	17774394	Missense_Mutation	NA	A279V	0.22
STAD	chr19	17776099	Missense_Mutation	rs148410831	E374K	0.26
UCEC	chr19	17776050	Missense_Mutation	NA	F357L	0.36
UCEC	chr19	17787722	Silent	NA	G841G	0.38
UCEC	chr19	17774266	Missense_Mutation	rs374509300	A273V	0.07
UCEC	chr19	17772536	Missense_Mutation	rs528053341	T225M	0.4
UCEC	chr19	17772672	Missense_Mutation	rs201978611	E241K	0.29
UCEC	chr19	17781516	Missense_Mutation	novel	S602N	0.12
UCEC	chr19	17784163	Silent	rs759256252	T718T	0.2
UCEC	chr19	17778150	Silent	novel	L425L	0.36
UCEC	chr19	17784228	Missense_Mutation	rs374251080	R740Q	0.48
UCEC	chr19	17764404	Missense_Mutation	NA	A50V	0.38
UCEC	chr19	17772458	Missense_Mutation	rs767365658	R199H	0.37
UCEC	chr19	17781265	Missense_Mutation	novel	R554S	0.1
UCEC	chr19	17784107	Missense_Mutation	NA	P700S	0.29
UCEC	chr19	17787728	Silent	novel	S843S	0.2
UCEC	chr19	17774252	Silent	rs144767216	F268F	0.13
UCEC	chr19	17774453	Missense_Mutation	NA	R299W	0.33
UCEC	chr19	17776089	Silent	NA	A370A	0.26
UCEC	chr19	17755131	5'UTR	novel		0.44
UCEC	chr19	17775062	Missense_Mutation	NA	F309L	0.21
UCEC	chr19	17774419	Missense_Mutation	NA	K287N	0.26
UCEC	chr19	17770828	Missense_Mutation	rs377605612	R176W	0.24
UCEC	chr19	17774435	Nonsense_Mutation	novel	G293*	0.17
UCEC	chr19	17774408	Missense_Mutation	rs142820853	R284W	0.2
UCEC	chr19	17783159	Missense_Mutation	rs376539312	D694N	0.35
UCEC	chr19	17770856	Missense_Mutation	novel	A185V	0.34
UCEC	chr19	17784132	Missense_Mutation	novel	K708R	0.32
UCEC	chr19	17787762	Missense_Mutation	novel	E855K	0.33
UCEC	chr19	17770847	Missense_Mutation	novel	Y182C	0.21
UCEC	chr19	17783073	Missense_Mutation	rs761547319	R665H	0.43
UCEC	chr19	17787820	Missense_Mutation	NA	S874L	0.18
UCEC	chr19	17770445	Silent	novel	S119S	0.46
UCEC	chr19	17776030	Missense_Mutation	rs780189734	D351N	0.3
UCEC	chr19	17776043	Missense_Mutation	rs199761608	R355H	0.41
UCEC	chr19	17762700	Intron	novel		0.22
UCEC	chr19	17783073	Missense_Mutation	rs761547319	R665H	0.46
UCEC	chr19	17775455	Splice_Site	novel	X316_splice	0.45
UCEC	chr19	17776050	Missense_Mutation	NA	F357L	0.35
UCEC	chr19	17781748	Missense_Mutation	novel	S622F	0.45
UCEC	chr19	17772653	Silent	novel	E234E	0.39
UCEC	chr19	17762724	Intron	novel		0.27
UCEC	chr19	17778176	Missense_Mutation	novel	K433N	0.58
UCEC	chr19	17764384	Silent	novel	I43I	0.6
UCEC	chr19	17783159	Missense_Mutation	rs376539312	D694N	0.37
UCEC	chr19	17762822	Missense_Mutation	novel	T30A	0.18
UCEC	chr19	17755130	5'UTR	rs374696612		0.28
UCEC	chr19	17776067	Missense_Mutation	NA	P363H	0.58
UCEC	chr19	17774425	Silent	novel	F289F	0.33
UCEC	chr19	17772479	Missense_Mutation	novel	T206I	0.11
UCEC	chr19	17762792	Missense_Mutation	NA	Y20D	0.31
UCEC	chr19	17770828	Missense_Mutation	rs377605612	R176W	0.32
UCEC	chr19	17776029	Silent	novel	D350D	0.28
UCEC	chr19	17778144	Nonsense_Mutation	novel	E423*	0.25
UCEC	chr19	17783084	Missense_Mutation	rs750801082	G669R	0.83
UCEC	chr19	17784194	Missense_Mutation	novel	P729S	0.42
UCEC	chr19	17772683	Silent	rs768979141	S244S	0.23
UCEC	chr19	17774266	Missense_Mutation	rs374509300	A273V	0.39
UCS	chr19	17788273	Intron	novel		0.52

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
READ	DEL	0.0848	0.23023
THCA	DEL	0.012	0.090402
THYM	DEL	0.0244	0.10691

Survival Analysis

Cancer	P-value	Q-value
THYM	0.023	Kaplan-Meier Survival Analysis
KIRC	0.0001	Kaplan-Meier Survival Analysis
STAD	0.0053	Kaplan-Meier Survival Analysis
ACC	0.05	Kaplan-Meier Survival Analysis
SKCM	0.00017	Kaplan-Meier Survival Analysis
PRAD	0.018	Kaplan-Meier Survival Analysis
COAD	0.019	Kaplan-Meier Survival Analysis
PCPG	0.039	Kaplan-Meier Survival Analysis
READ	0.00012	Kaplan-Meier Survival Analysis
KICH	0.044	Kaplan-Meier Survival Analysis
UCEC	0.0052	Kaplan-Meier Survival Analysis
LIHC	0.034	Kaplan-Meier Survival Analysis

Drugs

Cell lines and drugs in GSE70138 or GSE92742

Description

RBDs

Expression

Transcripts

Gene Model

Phenotypes

GWAS

PPI

Gene Ontology

Description

Ensembl ID: ENSG00000130475 (Gene tree)
Gene ID: 23149
Gene Symbol: FCHO1
Alias: KIAA0290
Full Name: FCH domain only 1
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Plus strand
Length: 40,851 bases
Position: chr19:17,747,718-17,788,568
Accession: 29002
RBP type: canonical RBP
Summary: FCHO1 (FCH Domain Only 1) is a Protein Coding gene. Among its related pathways are Clathrin-mediated endocytosis and Vesicle-mediated transport. Gene Ontology (GO) annotations related to this gene include AP-2 adaptor complex binding. An important paralog of this gene is FCHO2.

RNA binding domains(RBDs)

Protein ID	Domain	Pfam ID	E-value	Domain number	Total number
ENSP00000473173	U1snRNP70_N	PF12220.8	0.00022	1	1

Expression

Transcripts

Transcript ID	Name	Length	RefSeq ID	Protein ID	Length	RefSeq ID	UniportKB ID
ENST00000602111	FCHO1-236	781	-	-	- (aa)	-	-
ENST00000600058	FCHO1-230	910	-	-	- (aa)	-	-
ENST00000596536	FCHO1-216	3204	XM_006722701	ENSP00000470731	889 (aa)	XP_006722764	O14526
ENST00000598932	FCHO1-226	575	-	ENSP00000471563	101 (aa)	-	M0R107
ENST00000595549	FCHO1-209	774	-	ENSP00000470578	235 (aa)	-	M0QZI9
ENST00000600209	FCHO1-232	881	-	ENSP00000469075	175 (aa)	-	M0QXD1
ENST00000599236	FCHO1-228	586	-	-	- (aa)	-	-
ENST00000593385	FCHO1-202	573	-	ENSP00000471003	2 (aa)	-	UPI000005E811
ENST00000600201	FCHO1-231	694	-	-	- (aa)	-	-
ENST00000596951	FCHO1-218	2979	-	ENSP00000472417	889 (aa)	-	O14526
ENST00000595023	FCHO1-207	1131	-	ENSP00000471935	264 (aa)	-	M0R1K4
ENST00000593870	FCHO1-204	567	-	ENSP00000470068	35 (aa)	-	M0QYT8
ENST00000594068	FCHO1-205	841	-	ENSP00000469511	155 (aa)	-	M0QY09
ENST00000599766	FCHO1-229	747	-	-	- (aa)	-	-
ENST00000597512	FCHO1-221	2934	-	ENSP00000470568	896 (aa)	-	M0QZI3
ENST00000595749	FCHO1-211	562	-	-	- (aa)	-	-
ENST00000597474	FCHO1-220	556	-	ENSP00000470730	125 (aa)	-	M0QZS1
ENST00000598960	FCHO1-227	534	-	ENSP00000469967	23 (aa)	-	M0QYN8
ENST00000597076	FCHO1-219	501	-	-	- (aa)	-	-
ENST00000596507	FCHO1-214	1014	-	ENSP00000473169	218 (aa)	-	M0R3E5
ENST00000594202	FCHO1-206	3214	-	ENSP00000473001	891 (aa)	-	A0A0C3SFZ9
ENST00000596522	FCHO1-215	533	-	-	- (aa)	-	-
ENST00000598086	FCHO1-224	554	-	ENSP00000469425	111 (aa)	-	M0QXW2
ENST00000598539	FCHO1-225	551	-	ENSP00000469711	42 (aa)	-	M0QYA9
ENST00000596309	FCHO1-212	598	-	ENSP00000470511	92 (aa)	-	M0QZF0
ENST00000597718	FCHO1-222	884	-	ENSP00000473173	185 (aa)	-	M0R3E7
ENST00000596462	FCHO1-213	565	-	ENSP00000471450	15 (aa)	-	M0R0U5
ENST00000595594	FCHO1-210	898	-	-	- (aa)	-	-
ENST00000593833	FCHO1-203	580	-	ENSP00000470495	134 (aa)	-	M0QZE1
ENST00000601247	FCHO1-235	458	-	-	- (aa)	-	-
ENST00000596865	FCHO1-217	579	-	ENSP00000472623	97 (aa)	-	M0R2J7
ENST00000595033	FCHO1-208	2907	XM_005259831	ENSP00000472668	839 (aa)	XP_005259888	O14526
ENST00000252771	FCHO1-201	3118	-	ENSP00000252771	889 (aa)	-	O14526
ENST00000598067	FCHO1-223	543	-	ENSP00000469458	28 (aa)	-	M0QXY1
ENST00000600676	FCHO1-234	3094	XM_011527824	ENSP00000470493	889 (aa)	XP_011526126	O14526
ENST00000600393	FCHO1-233	597	-	-	- (aa)	-	-

Gene Model

Click here to download ENSG00000130475's gene model file

Phenotypes

ensgID	Trait	pValue	Pubmed ID
ENSG00000130475	Blood Pressure	1.5640000E-005	-
ENSG00000130475	Platelet Function Tests	3.9500000E-006	-
ENSG00000130475	Neoplasms	1E-13	23300138

GWAS

ensgID	SNP	Chromosome	Position	SNP-risk	Trait	PubmedID	95% CI	Or or BEAT	EFO ID
ENSG00000130475	rs12151113	19	17748561	T	Highest math class taken (MTAG)	30038396	[0.0058-0.0124] unit increase	0.0091	EFO_0004875

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000130475's network

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

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0005515	protein binding	19713939.25416956.	IPI	Function
GO:0005543	phospholipid binding	21873635.	IBA	Function
GO:0005654	nucleoplasm	-	IDA	Component
GO:0005737	cytoplasm	21873635.	IBA	Component
GO:0005829	cytosol	-	IDA	Component
GO:0005829	cytosol	-	TAS	Component
GO:0005856	cytoskeleton	21873635.	IBA	Component
GO:0005886	plasma membrane	21873635.	IBA	Component
GO:0005886	plasma membrane	20448150.	IDA	Component
GO:0005905	clathrin-coated pit	21873635.	IBA	Component
GO:0005905	clathrin-coated pit	20448150.22484487.	IDA	Component
GO:0008017	microtubule binding	21873635.	IBA	Function
GO:0008092	cytoskeletal protein binding	21873635.	IBA	Function
GO:0015631	tubulin binding	21873635.	IBA	Function
GO:0030122	AP-2 adaptor complex	21873635.	IBA	Component
GO:0030136	clathrin-coated vesicle	21873635.	IBA	Component
GO:0030136	clathrin-coated vesicle	20448150.	IDA	Component
GO:0035612	AP-2 adaptor complex binding	22484487.	IDA	Function
GO:0048268	clathrin coat assembly	21873635.	IBA	Process
GO:0048268	clathrin coat assembly	20448150.	IMP	Process
GO:0061024	membrane organization	-	TAS	Process
GO:0072583	clathrin-dependent endocytosis	21873635.	IBA	Process
GO:0072583	clathrin-dependent endocytosis	20448150.	IMP	Process
GO:0097320	plasma membrane tubulation	21873635.	IBA	Process

EuRBPDB

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Eesembl ID

Cell lines and drugs in GSE70138 or GSE92742

Description

RBDs

Expression

Transcripts

Gene Model

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.