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
BLCA	chr16	4361171	Missense_Mutation	novel	V589L	0.59
BLCA	chr16	4362078	Silent	rs775535940	L495L	0.28
BLCA	chr16	4362728	Missense_Mutation	novel	S429C	0.25
BLCA	chr16	4358478	Silent	rs752926019	L782L	0.33
BLCA	chr16	4360336	Missense_Mutation	rs200575254	G684R	0.15
BLCA	chr16	4361440	Silent	NA	T536T	0.27
BRCA	chr16	4354944	3'UTR	novel		0.47
BRCA	chr16	4362093	Silent	NA	L490L	0.25
BRCA	chr16	4362029	Missense_Mutation	NA	A512T	0.37
BRCA	chr16	4358083	Silent	rs555588403	D826D	0.31
CESC	chr16	4355095	3'UTR	rs562662030		0.26
CESC	chr16	4362622	Missense_Mutation	NA	Q464H	0.18
CESC	chr16	4360441	Splice_Region	novel		0.4
CESC	chr16	4358413	Missense_Mutation	rs774960939	R804H	0.3
CESC	chr16	4361928	Intron	novel		0.45
CESC	chr16	4361867	Intron	novel		0.22
CESC	chr16	4413379	Missense_Mutation	NA	G29E	0.22
CESC	chr16	4365046	Silent	NA	L285L	0.25
CESC	chr16	4416616	5'UTR	novel		0.29
CESC	chr16	4416617	5'UTR	novel		0.29
CESC	chr16	4357211	Missense_Mutation	rs369689601	A881V	0.25
CESC	chr16	4387991	Silent	rs764490402	S260S	0.35
CESC	chr16	4407556	Silent	rs754373086	S144S	0.61
CESC	chr16	4413374	Missense_Mutation	rs143239749	A31T	0.37
CESC	chr16	4412353	Splice_Region	novel		0.19
CESC	chr16	4362724	In_Frame_Ins	novel	S430_P431insND	0.17
CESC	chr16	4360477	Silent	NA	V663V	0.45
CESC	chr16	4359515	Missense_Mutation	NA	D739H	0.26
CHOL	chr16	4361852	Intron	novel		0.36
COAD	chr16	4407526	Silent	rs150918473	D154D	0.21
COAD	chr16	4364633	Silent	rs769559140	T367T	0.23
COAD	chr16	4355152	3'UTR	rs565553386		0.32
COAD	chr16	4357168	Missense_Mutation	novel	E895D	0.45
COAD	chr16	4358116	Intron	novel		0.15
COAD	chr16	4365031	Silent	rs140738162	V290V	0.11
COAD	chr16	4364281	Missense_Mutation	rs761999840	A424T	0.44
COAD	chr16	4355120	3'UTR	novel		0.4
COAD	chr16	4360337	Silent	rs199645423	R683R	0.47
COAD	chr16	4408250	Missense_Mutation	novel	D78E	0.5
COAD	chr16	4362703	Silent	rs769374019	S437S	0.33
COAD	chr16	4358286	Intron	novel		0.48
COAD	chr16	4358477	Missense_Mutation	rs201255366	V783I	0.19
COAD	chr16	4364632	Missense_Mutation	rs748161669	D368N	0.13
COAD	chr16	4388578	Silent	NA	T223T	0.29
COAD	chr16	4407555	Missense_Mutation	rs766048891	A145T	0.35
COAD	chr16	4358374	Missense_Mutation	rs768577818	R817Q	0.25
COAD	chr16	4364672	Missense_Mutation	rs775838457	E354D	0.34
COAD	chr16	4405500	Silent	rs753464714	T185T	0.16
COAD	chr16	4358019	Missense_Mutation	NA	A848T	0.19
COAD	chr16	4359577	Missense_Mutation	novel	A718V	0.34
COAD	chr16	4395302	Missense_Mutation	rs200117600	P201L	0.19
ESCA	chr16	4362734	Missense_Mutation	novel	G427D	0.33
ESCA	chr16	4357995	Missense_Mutation	novel	S856G	0.68
ESCA	chr16	4358368	Missense_Mutation	rs569079730	R819Q	0.33
ESCA	chr16	4362008	Missense_Mutation	rs746084994	G519R	0.42
ESCA	chr16	4364632	Missense_Mutation	rs748161669	D368N	0.21
GBM	chr16	4364381	Silent	NA	R390R	0.52
GBM	chr16	4358276	Intron	novel		0.55
GBM	chr16	4361453	Missense_Mutation	rs755060334	R532H	0.11
GBM	chr16	4388056	Missense_Mutation	rs577087075	E239K	0.25
GBM	chr16	4357969	Splice_Region	novel	P864P	0.16
GBM	chr16	4358020	Silent	rs776114367	G847G	0.1
GBM	chr16	4359375	Missense_Mutation	rs765337019	R754H	0.38
HNSC	chr16	4361953	Intron	novel		0.33
HNSC	chr16	4416607	5'UTR	rs749992337		0.46
KICH	chr16	4395318	Missense_Mutation	novel	D196N	0.11
KIRC	chr16	4362075	Silent	rs771924133	T496T	0.38
KIRC	chr16	4358460	Silent	rs151072609	T788T	0.19
KIRC	chr16	4355286	Missense_Mutation	NA	W924C	0.4
KIRP	chr16	4358274	Intron	novel		0.55
LGG	chr16	4359611	Missense_Mutation	rs774571246	R707C	0.46
LGG	chr16	4362703	Silent	rs769374019	S437S	0.52
LGG	chr16	4364654	Silent	novel	T360T	0.6
LIHC	chr16	4355165	Splice_Site	novel	X925_splice	0.14
LIHC	chr16	4364674	Nonsense_Mutation	novel	E354*	0.25
LUAD	chr16	4360326	Missense_Mutation	rs768734194	I687T	0.08
LUAD	chr16	4355288	In_Frame_Ins	novel	D922_E923dup	0.09
LUAD	chr16	4361087	Splice_Site	NA	X592_splice	0.26
LUAD	chr16	4358034	Missense_Mutation	NA	A843S	0.27
LUAD	chr16	4358222	Intron	novel		0.25
LUAD	chr16	4360487	Missense_Mutation	NA	R660L	0.38
LUAD	chr16	4361440	Silent	novel	T536T	0.43
LUAD	chr16	4405509	Silent	novel	L182L	0.08
LUAD	chr16	4358120	Intron	novel		0.34
LUAD	chr16	4358436	Missense_Mutation	NA	E796D	0.57
LUAD	chr16	4358411	Nonsense_Mutation	novel	Q805*	0.12
LUSC	chr16	4364341	Frame_Shift_Del	novel	*E404Sfs11**	0.69
LUSC	chr16	4365024	Nonsense_Mutation	NA	Q293*	0.67
LUSC	chr16	4365001	Splice_Site	NA	X300_splice	0.31
LUSC	chr16	4364383	Missense_Mutation	rs370284503	R390W	0.2
LUSC	chr16	4361465	Missense_Mutation	rs200108761	R528Q	0.56
LUSC	chr16	4359600	Silent	rs749496892	L710L	0.4
LUSC	chr16	4360972	Missense_Mutation	rs140152390	R630W	0.52
LUSC	chr16	4361024	Silent	novel	S612S	0.54
LUSC	chr16	4364312	Silent	rs373254304	A413A	0.35
LUSC	chr16	4358415	Silent	novel	L803L	0.44
LUSC	chr16	4364873	Missense_Mutation	NA	P316A	0.43
LUSC	chr16	4357254	Nonsense_Mutation	NA	Q867*	0.85
OV	chr16	4364869	Missense_Mutation	NA	R317P	0.37
OV	chr16	4358189	Intron	novel		0.44
PAAD	chr16	4359542	Missense_Mutation	novel	A730T	0.15
PCPG	chr16	4358409	Silent	rs763232660	Q805Q	0.41
PRAD	chr16	4358306	Intron	novel		0.65
PRAD	chr16	4357210	Silent	rs148065861	A881A	0.29
PRAD	chr16	4360481	Missense_Mutation	rs201929828	R662Q	0.33
PRAD	chr16	4361453	Missense_Mutation	rs755060334	R532H	0.5
PRAD	chr16	4364862	Silent	rs758151484	A319A	0.29
READ	chr16	4361002	Missense_Mutation	rs766836793	R620S	0.23
READ	chr16	4405501	Missense_Mutation	rs778533107	T185M	0.47
SARC	chr16	4361429	Missense_Mutation	rs200682379	T540M	0.34
SARC	chr16	4361428	Silent	rs776723227	T540T	0.15
SARC	chr16	4408229	Silent	rs770183012	F85F	0.35
SKCM	chr16	4361195	Missense_Mutation	novel	E581K	0.49
SKCM	chr16	4362713	Missense_Mutation	rs759601582	S434L	0.63
SKCM	chr16	4364374	Missense_Mutation	NA	P393S	0.38
SKCM	chr16	4413324	Silent	NA	F47F	0.57
SKCM	chr16	4362724	Silent	NA	S430S	0.27
SKCM	chr16	4359353	Silent	NA	L761L	0.17
SKCM	chr16	4361378	Missense_Mutation	rs113335841	P557L	0.22
SKCM	chr16	4360482	Silent	novel	R662R	0.29
SKCM	chr16	4357227	Missense_Mutation	rs374424650	R876W	0.11
SKCM	chr16	4358128	Intron	novel		0.5
SKCM	chr16	4358349	Intron	novel		0.31
SKCM	chr16	4362713	Missense_Mutation	rs759601582	S434L	0.24
SKCM	chr16	4359335	Silent	NA	F767F	0.21
SKCM	chr16	4416525	5'UTR	rs375292869		0.29
SKCM	chr16	4416526	5'UTR	novel		0.29
SKCM	chr16	4358369	Missense_Mutation	rs373678474	R819W	0.13
SKCM	chr16	4358370	Silent	novel	V818V	0.13
SKCM	chr16	4358058	Missense_Mutation	NA	W835R	0.33
SKCM	chr16	4361247	Splice_Region	novel	A563A	0.45
SKCM	chr16	4361248	Missense_Mutation	novel	A563V	0.44
SKCM	chr16	4358176	Intron	novel		0.29
SKCM	chr16	4361373	Missense_Mutation	rs147901888	R559C	0.25
SKCM	chr16	4362725	Missense_Mutation	NA	S430F	0.4
SKCM	chr16	4364790	Silent	rs755640512	Y343Y	0.5
SKCM	chr16	4357925	Intron	novel		0.56
SKCM	chr16	4357890	Intron	novel		0.41
STAD	chr16	4407511	Missense_Mutation	novel	Q159H	0.83
STAD	chr16	4360337	Silent	rs199645423	R683R	0.26
STAD	chr16	4359527	Missense_Mutation	NA	L735M	0.37
STAD	chr16	4416623	5'UTR	novel		0.5
STAD	chr16	4365044	Missense_Mutation	NA	Y286C	0.27
STAD	chr16	4357751	Intron	novel		1
STAD	chr16	4359581	Missense_Mutation	NA	L717M	0.5
STAD	chr16	4364844	Silent	rs139939383	C325C	0.42
STAD	chr16	4359545	Missense_Mutation	rs200550834	V729M	0.16
STAD	chr16	4358007	Missense_Mutation	NA	P852S	0.15
STAD	chr16	4413374	Missense_Mutation	rs143239749	A31T	0.27
STAD	chr16	4358306	Intron	novel		0.4
STAD	chr16	4361441	Missense_Mutation	rs145925246	T536M	0.31
STAD	chr16	4362677	Missense_Mutation	NA	P446H	0.24
STAD	chr16	4361079	Missense_Mutation	rs201451820	T594M	0.19
STAD	chr16	4407672	Nonsense_Mutation	rs745958172	R106*	0.29
THCA	chr16	4361172	Silent	NA	T588T	0.34
THCA	chr16	4359368	Missense_Mutation	novel	F756L	0.24
THCA	chr16	4359334	Silent	novel	L768L	0.18
THCA	chr16	4359335	Silent	NA	F767F	0.18
THYM	chr16	4364633	Silent	rs769559140	T367T	0.12
UCEC	chr16	4361018	Silent	NA	S614S	0.43
UCEC	chr16	4362713	Missense_Mutation	rs759601582	S434L	0.32
UCEC	chr16	4354935	3'UTR	novel		0.19
UCEC	chr16	4359602	Missense_Mutation	novel	L710F	0.15
UCEC	chr16	4362146	Missense_Mutation	novel	F473V	0.39
UCEC	chr16	4360546	Splice_Region	novel	I640I	0.44
UCEC	chr16	4364843	Missense_Mutation	rs147491703	E326K	0.42
UCEC	chr16	4354875	3'UTR	novel		0.27
UCEC	chr16	4359563	Missense_Mutation	novel	A723S	0.18
UCEC	chr16	4361238	Silent	rs772815248	D566D	0.36
UCEC	chr16	4364848	Missense_Mutation	novel	S324N	0.45
UCEC	chr16	4354723	3'UTR	novel		0.36
UCEC	chr16	4359321	Missense_Mutation	novel	S772I	0.38
UCEC	chr16	4359575	Missense_Mutation	rs373350704	G719S	0.47
UCEC	chr16	4361372	Missense_Mutation	rs142371956	R559H	0.48
UCEC	chr16	4361086	Splice_Site	NA	X592_splice	0.21
UCEC	chr16	4355030	3'UTR	novel		0.24
UCEC	chr16	4358454	Silent	rs768413907	C790C	0.36
UCEC	chr16	4358038	Silent	rs745478194	A841A	0.16
UCEC	chr16	4361362	Splice_Region	novel	V562V	0.14
UCEC	chr16	4355126	3'UTR	novel		0.22
UCEC	chr16	4358175	Intron	novel		0.5
UCEC	chr16	4360509	Missense_Mutation	NA	A653T	0.19
UCEC	chr16	4361462	Missense_Mutation	novel	K529T	0.45
UCEC	chr16	4355036	3'UTR	novel		0.38
UCEC	chr16	4361229	Silent	novel	I569I	0.08
UCEC	chr16	4365530	Silent	novel	L267L	0.27
UCEC	chr16	4364856	Silent	rs750175369	A321A	0.27
UCEC	chr16	4361373	Missense_Mutation	rs147901888	R559C	0.19
UCEC	chr16	4395302	Missense_Mutation	novel	P201Q	0.17
UCEC	chr16	4355304	Silent	rs756395820	G918G	0.48
UCEC	chr16	4355313	Silent	novel	S915S	0.57
UCEC	chr16	4358414	Missense_Mutation	rs375655768	R804C	0.4
UCEC	chr16	4354895	3'UTR	novel		0.39
UCEC	chr16	4360534	Silent	NA	A644A	0.14
UCEC	chr16	4364869	Missense_Mutation	rs556405302	R317Q	0.3
UCEC	chr16	4408241	Silent	rs368877158	T81T	0.4
UCEC	chr16	4407525	Missense_Mutation	rs775952526	A155T	0.38
UCEC	chr16	4388602	Missense_Mutation	novel	D215E	0.21
UCEC	chr16	4362713	Missense_Mutation	rs759601582	S434L	0.24
UCEC	chr16	4360466	Missense_Mutation	rs372806628	R667Q	0.42
UCEC	chr16	4388058	Missense_Mutation	rs138528740	R238H	0.21
UCEC	chr16	4413385	Missense_Mutation	rs188785592	R27Q	0.38
UCEC	chr16	4407672	Nonsense_Mutation	rs745958172	R106*	0.24
UCEC	chr16	4358420	Missense_Mutation	rs139564699	R802W	0.32
UCEC	chr16	4364833	Missense_Mutation	rs201907324	R329H	0.49
UCEC	chr16	4407672	Nonsense_Mutation	rs745958172	R106*	0.62
UCEC	chr16	4361395	Silent	novel	A551A	0.33
UCEC	chr16	4354924	3'UTR	novel		0.1
UCEC	chr16	4413329	Missense_Mutation	rs527794334	A46T	0.4
UCEC	chr16	4355072	3'UTR	novel		0.63
UCEC	chr16	4364632	Missense_Mutation	rs748161669	D368N	0.5
UCEC	chr16	4359485	Missense_Mutation	rs746919528	G749S	0.21
UCEC	chr16	4361002	Missense_Mutation	novel	R620C	0.44
UCEC	chr16	4365028	Silent	novel	V291V	0.33
UCEC	chr16	4357907	Intron	novel		0.09
UCEC	chr16	4407662	Missense_Mutation	novel	G109V	0.27
UCEC	chr16	4359532	Missense_Mutation	novel	T733N	0.26
UCEC	chr16	4358100	Nonsense_Mutation	NA	E821*	0.65
UCEC	chr16	4357786	Intron	novel		0.8
UCEC	chr16	4405497	Silent	rs751954259	A186A	0.19
UCEC	chr16	4364805	Silent	rs772271708	I338I	0.07
UCEC	chr16	4359534	Silent	novel	S732S	0.47
UCEC	chr16	4361924	Intron	novel		0.4
UCEC	chr16	4364804	Missense_Mutation	rs112630763	V339M	0.41

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
ACC	AMP	0.5444	0.22898
CHOL	DEL	0.1111	0.23475

Survival Analysis

Cancer	P-value	Q-value
KIRC	0.0001	Kaplan-Meier Survival Analysis
HNSC	0.048	Kaplan-Meier Survival Analysis
BRCA	0.006	Kaplan-Meier Survival Analysis
ESCA	0.039	Kaplan-Meier Survival Analysis
PAAD	0.0059	Kaplan-Meier Survival Analysis
PCPG	0.022	Kaplan-Meier Survival Analysis
BLCA	0.014	Kaplan-Meier Survival Analysis
CESC	0.00013	Kaplan-Meier Survival Analysis
LAML	0.0013	Kaplan-Meier Survival Analysis
KICH	0.023	Kaplan-Meier Survival Analysis
UCEC	0.0016	Kaplan-Meier Survival Analysis
LIHC	0.0017	Kaplan-Meier Survival Analysis
LGG	0.0001	Kaplan-Meier Survival Analysis
LUAD	0.0019	Kaplan-Meier Survival Analysis
UVM	0.0014	Kaplan-Meier Survival Analysis

Drugs

Cell lines and drugs in GSE70138 or GSE92742

Description

RBPome

Expression

Transcripts

Gene Model

Phenotypes

GWAS

PPI

Gene Ontology

Description

Ensembl ID: ENSG00000262246 (Gene tree)
Gene ID: 79585
Gene Symbol: CORO7
Alias: FLJ22021
Full Name: coronin 7
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Minus strand
Length: 71,164 bases
Position: chr16:4,354,542-4,425,705
Accession: 26161
RBP type: non-canonical RBP
Summary: This gene encodes a member of the coronin protein family. However, unlike other coronin proteins, it is not an actin-binding protein but rather functions as an F-actin regulator directing anterograde Golgi to endosome transport. The encoded protein has two tandem WD-40 domain repeats and localizes to the trans-Golgi network. The protein undergoes K33-linked polyubiquitination via an E3 ligase complex. It is thought to play an essential role in maintenance of Golgi apparatus morphology. Alternative splicing results in multiple transcripts variants; some of which form read-through transcripts with a neighboring gene. [provided by RefSeq, Dec 2016]

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
ENST00000572549	CORO7-216	663	-	ENSP00000459286	205 (aa)	-	I3L212
ENST00000572140	CORO7-213	478	-	-	- (aa)	-	-
ENST00000572125	CORO7-212	681	-	-	- (aa)	-	-
ENST00000537233	CORO7-202	3392	-	ENSP00000440460	907 (aa)	-	P57737
ENST00000576457	CORO7-231	571	-	-	- (aa)	-	-
ENST00000570928	CORO7-205	540	-	ENSP00000460199	114 (aa)	-	I3L359
ENST00000576637	CORO7-232	730	-	ENSP00000460177	119 (aa)	-	I3L351
ENST00000572898	CORO7-218	593	-	ENSP00000458935	161 (aa)	-	I3L1M1
ENST00000576437	CORO7-230	1066	-	ENSP00000459228	108 (aa)	-	I3L1Z1
ENST00000575038	CORO7-225	832	-	ENSP00000461797	201 (aa)	-	I3NI06
ENST00000575714	CORO7-227	2978	-	-	- (aa)	-	-
ENST00000573165	CORO7-219	729	-	ENSP00000459401	19 (aa)	-	I3L258
ENST00000575850	CORO7-228	666	-	ENSP00000460910	206 (aa)	-	I3L426
ENST00000572518	CORO7-215	546	-	-	- (aa)	-	-
ENST00000571756	CORO7-209	1890	-	ENSP00000458828	219 (aa)	-	I3L1G9
ENST00000572666	CORO7-217	1237	-	-	- (aa)	-	-
ENST00000570645	CORO7-203	501	-	ENSP00000460901	47 (aa)	-	I3L423
ENST00000573245	CORO7-220	443	-	-	- (aa)	-	-
ENST00000576051	CORO7-229	557	-	ENSP00000459888	11 (aa)	-	I3L2S7
ENST00000574849	CORO7-224	490	-	-	- (aa)	-	-
ENST00000572026	CORO7-210	586	-	-	- (aa)	-	-
ENST00000572153	CORO7-214	548	-	ENSP00000461051	46 (aa)	-	I3L482
ENST00000572044	CORO7-211	563	-	ENSP00000458411	161 (aa)	-	I3L0X8
ENST00000573773	CORO7-221	934	-	-	- (aa)	-	-
ENST00000251166	CORO7-201	3540	-	ENSP00000251166	925 (aa)	-	P57737
ENST00000570779	CORO7-204	605	-	ENSP00000460956	190 (aa)	-	I3L442
ENST00000571227	CORO7-208	3578	-	ENSP00000458459	46 (aa)	-	I3L0Z7
ENST00000574025	CORO7-222	2826	-	ENSP00000461702	840 (aa)	-	P57737
ENST00000571059	CORO7-207	581	-	ENSP00000460036	156 (aa)	-	I3L2Y6
ENST00000571052	CORO7-206	578	-	ENSP00000459085	57 (aa)	-	I3L1T5
ENST00000574311	CORO7-223	1737	-	ENSP00000461187	367 (aa)	-	E7EP81
ENST00000577144	CORO7-233	618	-	-	- (aa)	-	-
ENST00000575531	CORO7-226	2636	-	-	- (aa)	-	-

Gene Model

Click here to download ENSG00000262246's gene model file

Phenotypes

ensgID	Trait	pValue	Pubmed ID
ENSG00000262246	Hip	7E-9	25673412
ENSG00000262246	Body Mass Index	7E-9	25673412
ENSG00000262246	Hip	6E-6	25673412
ENSG00000262246	Body Mass Index	6E-6	25673412

GWAS

ensgID	SNP	Chromosome	Position	SNP-risk	Trait	PubmedID	95% CI	Or or BEAT	EFO ID
ENSG00000262246	rs6500596	16	4420026	G	Schizophrenia	28991256	[1.04-1.09]	1.0649627	EFO_0000692
ENSG00000262246	rs757593	16	4391616	A	Self-reported math ability	30038396	[0.0094-0.018] unit decrease	0.0137	EFO_0004875
ENSG00000262246	rs757593	16	4391616	A	Self-reported math ability (MTAG)	30038396	[0.0094-0.0172] unit decrease	0.0133	EFO_0004875
ENSG00000262246	rs757593	16	4391616	A	Highest math class taken (MTAG)	30038396	[0.0071-0.0145] unit decrease	0.0108	EFO_0004875
ENSG00000262246	rs3747579	16	4395326	T	Hip circumference adjusted for BMI	25673412	[0.015-0.031] unit increase	0.0231	EFO_0008039
ENSG00000262246	rs3747579	16	4395326	T	Hip circumference adjusted for BMI	25673412	[0.013-0.033] unit increase	0.0231	EFO_0008039
ENSG00000262246	rs8052826	16	4375527	?	Heel bone mineral density	30048462	[0.013-0.023] unit increase	0.0184003	EFO_0009270
ENSG00000262246	rs148092711	16	4381766	?	Heel bone mineral density	30048462	[0.067-0.123] unit increase	0.0950537	EFO_0009270
ENSG00000262246	rs4786488	16	4392526	?	Heel bone mineral density	30048462	[0.0098-0.019] unit increase	0.0143967	EFO_0009270
ENSG00000262246	rs8052826	16	4375527	A	Heel bone mineral density	30598549	[0.0091-0.018] unit increase	0.0135224	EFO_0009270
ENSG00000262246	rs148092711	16	4381766	C	Heel bone mineral density	30598549	[0.072-0.123] unit increase	0.0974273	EFO_0009270
ENSG00000262246	rs75345455	16	4369853	?	Systolic blood pressure	30595370			EFO_0006335
ENSG00000262246	rs7200336	16	4372606	?	Waist-hip ratio	30595370			EFO_0004343
ENSG00000262246	rs6500596	16	4420026	G	Schizophrenia	30285260	[1.04-1.09]	1.0632641	EFO_0000692
ENSG00000262246	rs11648292	16	4412896	?	Eosinophil counts	30595370			EFO_0004842
ENSG00000262246	rs8052826	16	4375527	?	Heel bone mineral density	30595370			EFO_0009270
ENSG00000262246	rs6500596	16	4420026	G	Schizophrenia	30285260	[1.04-1.08]	1.0582011	EFO_0000692
ENSG00000262246	rs3747579	16	4395326	C	Waist-to-hip ratio adjusted for BMI (additive genetic model)	30778226	[0.013-0.022] unit increase	0.0177	EFO_0007788
ENSG00000262246	rs3810818	16	4382028	A	Waist-to-hip ratio adjusted for BMI (additive genetic model)	30778226	[0.011-0.021] unit increase	0.0158	EFO_0007788
ENSG00000262246	rs3747579	16	4395326	C	Waist-to-hip ratio adjusted for BMI (additive genetic model)	30778226	[0.013-0.023] unit increase	0.0179	EFO_0007788
ENSG00000262246	rs3810818	16	4382028	A	Waist-to-hip ratio adjusted for BMI (additive genetic model)	30778226	[0.01-0.021] unit increase	0.0157	EFO_0007788
ENSG00000262246	rs3747579	16	4395326	C	Waist-to-hip ratio adjusted for BMI (additive genetic model)	30778226	[0.016-0.029] unit increase	0.0225	EFO_0007788
ENSG00000262246	rs3810818	16	4382028	A	Waist-to-hip ratio adjusted for BMI (additive genetic model)	30778226	[0.01-0.026] unit increase	0.0179	EFO_0007788
ENSG00000262246	rs3747579	16	4395326	C	Waist-to-hip ratio adjusted for BMI (additive genetic model)	30778226	[0.016-0.029] unit increase	0.0221	EFO_0007788
ENSG00000262246	rs3810818	16	4382028	A	Waist-to-hip ratio adjusted for BMI (additive genetic model)	30778226	[0.011-0.026] unit increase	0.0185	EFO_0007788

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000262246's network

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0000139	Golgi membrane	-	IEA	Component
GO:0003779	actin binding	24768539.	IDA	Function
GO:0005515	protein binding	21130766.24768539.	IPI	Function
GO:0005794	Golgi apparatus	-	ISS	Component
GO:0005802	trans-Golgi network	24768539.	IDA	Component
GO:0005829	cytosol	-	IEA	Component
GO:0006895	Golgi to endosome transport	24768539.	IMP	Process
GO:0015031	protein transport	-	IEA	Process
GO:0016020	membrane	19946888.	HDA	Component
GO:0016021	integral component of membrane	-	ISS	Component
GO:0030041	actin filament polymerization	24768539.	IMP	Process
GO:0031410	cytoplasmic vesicle	-	IEA	Component

EuRBPDB

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Gene Ontology

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