EuRBPDB

Note: to get the extension of tumor abbreviations.

Cancer Related Information
Basic Information

Cancer associated literatures

PID	Title	Article	Time	Author	Doi
23920402	WD40 repeat-containing 62 overexpression as a novel indicator of poor prognosis for human gastric cancer.	Eur J Cancer	2013 Nov	Zeng S	doi: 10.1016/j.ejca.2013.07.015
28277612	WDR62 overexpression is associated with a poor prognosis in patients with lung adenocarcinoma.	Mol Carcinog	2017 Aug	Shinmura K	doi: 10.1002/mc.22647

Differential Expression

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq
ACC	chr19	36083154	Missense_Mutation	novel	P488R	0.52
ACC	chr19	36090521	Splice_Site	novel	X678_splice	0.13
BLCA	chr19	36103400	Missense_Mutation	novel	D1186G	0.14
BLCA	chr19	36102781	Missense_Mutation	NA	E1084K	0.22
BLCA	chr19	36103363	Missense_Mutation	novel	A1174T	0.19
BLCA	chr19	36094080	Missense_Mutation	novel	G795R	0.09
BLCA	chr19	36059971	Missense_Mutation	novel	C91W	0.12
BLCA	chr19	36083141	Missense_Mutation	NA	E484K	0.08
BLCA	chr19	36081479	Missense_Mutation	novel	S427F	0.43
BLCA	chr19	36103075	Splice_Site	rs369923535	X1149_splice	0.16
BLCA	chr19	36100751	Missense_Mutation	NA	E915K	0.13
BLCA	chr19	36103879	Missense_Mutation	novel	P1346S	0.27
BLCA	chr19	36067364	Missense_Mutation	novel	S207L	0.45
BLCA	chr19	36067845	Silent	novel	P239P	0.36
BLCA	chr19	36099517	Missense_Mutation	NA	Q880R	0.42
BRCA	chr19	36089060	Missense_Mutation	novel	I597M	0.08
BRCA	chr19	36086805	Silent	NA	K587K	0.27
BRCA	chr19	36099556	Missense_Mutation	NA	S893N	0.14
BRCA	chr19	36067342	Missense_Mutation	novel	R200G	0.13
BRCA	chr19	36094083	Missense_Mutation	NA	E796K	0.17
BRCA	chr19	36067975	Missense_Mutation	NA	E283Q	0.24
BRCA	chr19	36083181	Missense_Mutation	NA	V497G	0.14
BRCA	chr19	36094092	Missense_Mutation	NA	E799K	0.27
BRCA	chr19	36103364	Missense_Mutation	rs372642550	A1174V	0.2
BRCA	chr19	36086722	Missense_Mutation	novel	L560V	0.22
BRCA	chr19	36094081	Missense_Mutation	rs773240057	G795E	0.53
BRCA	chr19	36102824	In_Frame_Del	novel	L1099_L1102del	0.16
CESC	chr19	36099471	Missense_Mutation	novel	A865T	0.28
CESC	chr19	36104661	Missense_Mutation	NA	D1428H	0.18
CESC	chr19	36054962	5'Flank	novel		0.19
CESC	chr19	36102748	Splice_Region	rs373781801		0.47
CESC	chr19	36073739	Intron	novel		0.14
CESC	chr19	36060105	Intron	novel		0.33
CESC	chr19	36089284	Missense_Mutation	novel	A646S	0.09
CESC	chr19	36084677	Silent	rs192491678	D525D	0.32
CESC	chr19	36103768	Missense_Mutation	NA	D1309N	0.49
CESC	chr19	36102967	Missense_Mutation	NA	P1114S	0.42
COAD	chr19	36099439	Missense_Mutation	NA	A854V	0.38
COAD	chr19	36066301	Missense_Mutation	novel	K145N	0.11
COAD	chr19	36055131	Missense_Mutation	novel	E54K	0.21
COAD	chr19	36073419	Missense_Mutation	novel	L374Q	0.31
COAD	chr19	36104586	Missense_Mutation	NA	P1403S	0.29
COAD	chr19	36101310	Silent	rs762321869	P988P	0.31
COAD	chr19	36102762	Silent	rs749825052	D1077D	0.49
COAD	chr19	36083077	Silent	rs776551919	V462V	0.3
COAD	chr19	36083228	Missense_Mutation	novel	S513R	0.26
COAD	chr19	36089280	Silent	NA	A644A	0.21
COAD	chr19	36102018	Silent	rs141344823	C1029C	0.2
COAD	chr19	36099478	Missense_Mutation	rs757558839	R867Q	0.32
COAD	chr19	36092796	Missense_Mutation	rs762688861	R773Q	0.48
COAD	chr19	36083178	Missense_Mutation	rs760351175	R496Q	0.5
COAD	chr19	36103886	Missense_Mutation	rs753208163	S1348F	0.16
COAD	chr19	36104891	Missense_Mutation	NA	A1474T	0.32
COAD	chr19	36091433	Silent	novel	D726D	0.16
COAD	chr19	36086740	Missense_Mutation	rs145392484	V566M	0.44
COAD	chr19	36089091	Missense_Mutation	rs553327137	R608C	0.37
COAD	chr19	36103162	Missense_Mutation	NA	A1152S	0.32
COAD	chr19	36073385	Missense_Mutation	rs779070171	V363M	0.33
ESCA	chr19	36083083	Nonsense_Mutation	novel	Y464*	0.07
ESCA	chr19	36101262	Silent	rs781264395	G972G	0.13
ESCA	chr19	36071682	Missense_Mutation	novel	L337V	0.41
GBM	chr19	36099499	Missense_Mutation	novel	K874M	0.18
GBM	chr19	36083202	Missense_Mutation	novel	G504V	0.13
GBM	chr19	36084740	Missense_Mutation	novel	E546D	0.13
GBM	chr19	36089196	Silent	novel	G616G	0.5
GBM	chr19	36094053	Missense_Mutation	novel	P786T	0.24
GBM	chr19	36071662	Missense_Mutation	novel	N330S	0.23
HNSC	chr19	36071657	Silent	rs200298843	L328L	0.11
HNSC	chr19	36081435	Splice_Region	novel	V412V	0.48
HNSC	chr19	36105001	Silent	novel	A1510A	0.31
HNSC	chr19	36071613	Missense_Mutation	rs766074970	D314N	0.42
HNSC	chr19	36067419	Silent	novel	F225F	0.15
HNSC	chr19	36081488	Missense_Mutation	novel	T430I	0.11
HNSC	chr19	36102781	Missense_Mutation	NA	E1084K	0.11
HNSC	chr19	36103879	Missense_Mutation	novel	P1346A	0.13
HNSC	chr19	36092796	Missense_Mutation	rs762688861	R773Q	0.3
HNSC	chr19	36066342	Missense_Mutation	novel	A159E	0.5
HNSC	chr19	36083066	Silent	novel	L459L	0.26
KICH	chr19	36067948	Frame_Shift_Ins	novel	*S275Tfs20**	0.47
KIRC	chr19	36083172	Missense_Mutation	NA	G494E	0.4
KIRC	chr19	36060152	Intron	novel		0.15
KIRP	chr19	36091276	Missense_Mutation	rs750547223	S704L	0.16
LAML	chr19	36067374	Silent	novel	S210S	0.12
LGG	chr19	36099544	In_Frame_Ins	novel	K890_P891dup	0.39
LGG	chr19	36090494	Nonsense_Mutation	novel	*Q670Rfs5**	0.17
LGG	chr19	36081554	Missense_Mutation	NA	K452I	0.19
LGG	chr19	36060045	Intron	novel		0.09
LGG	chr19	36103833	Silent	rs778940951	S1330S	0.41
LIHC	chr19	36091252	Missense_Mutation	novel	S696N	0.31
LIHC	chr19	36054941	5'Flank	novel		0.35
LIHC	chr19	36101297	Missense_Mutation	novel	K984M	0.23
LIHC	chr19	36055025	Silent	novel	L18L	0.66
LUAD	chr19	36060047	Intron	novel		0.14
LUAD	chr19	36073447	Silent	novel	I383I	0.07
LUAD	chr19	36066423	Missense_Mutation	NA	W186L	0.9
LUAD	chr19	36073496	Missense_Mutation	novel	E400K	0.16
LUAD	chr19	36094095	Missense_Mutation	novel	D800N	0.16
LUAD	chr19	36099479	Silent	novel	R867R	0.43
LUAD	chr19	36071685	Missense_Mutation	NA	G338W	0.09
LUAD	chr19	36071697	Missense_Mutation	NA	A342S	0.7
LUAD	chr19	36089101	Missense_Mutation	NA	Q611L	0.21
LUAD	chr19	36097032	Missense_Mutation	NA	R825C	0.88
LUAD	chr19	36089185	Missense_Mutation	novel	G613C	0.18
LUAD	chr19	36086766	Missense_Mutation	novel	Q574H	0.2
LUAD	chr19	36067826	Splice_Site	NA	X234_splice	0.18
LUAD	chr19	36060079	Intron	novel		0.56
LUSC	chr19	36104546	Silent	novel	P1389P	0.22
LUSC	chr19	36060062	Intron	novel		0.19
LUSC	chr19	36055110	Nonsense_Mutation	NA	R47*	0.39
LUSC	chr19	36103355	Missense_Mutation	NA	T1171M	0.27
LUSC	chr19	36089060	Silent	novel	I597I	0.22
LUSC	chr19	36066016	Splice_Site	novel	X130_splice	0.65
LUSC	chr19	36060023	Missense_Mutation	novel	T109S	0.57
LUSC	chr19	36094142	Frame_Shift_Del	novel	*K817Rfs23**	0.05
LUSC	chr19	36066255	Splice_Site	NA	X131_splice	0.26
LUSC	chr19	36067916	Missense_Mutation	NA	G263A	0.38
LUSC	chr19	36100841	Missense_Mutation	novel	L945V	0.42
LUSC	chr19	36058826	Missense_Mutation	NA	G75V	0.21
MESO	chr19	36104932	Silent	rs746402119	T1487T	0.68
OV	chr19	36090480	Missense_Mutation	novel	C665Y	0.07
OV	chr19	36067366	Missense_Mutation	novel	E208Q	0.13
OV	chr19	36084657	Frame_Shift_Del	novel	*E520Gfs10**	0.1
OV	chr19	36102079	Silent	novel	L1050L	0.22
OV	chr19	36092782	Nonsense_Mutation	novel	T768_N769ins*	0.24
OV	chr19	36103024	Missense_Mutation	rs750117864	G1133R	0.56
OV	chr19	36058869	Splice_Region	novel	A89A	0.29
OV	chr19	36065957	Splice_Site	novel	X111_splice	0.08
OV	chr19	36104671	Missense_Mutation	rs146018199	R1431H	0.5
OV	chr19	36071651	Silent	novel	H326H	0.4
OV	chr19	36067315	Missense_Mutation	novel	V191L	0.04
OV	chr19	36091218	Missense_Mutation	novel	G685S	0.12
PAAD	chr19	36081512	Missense_Mutation	novel	R438L	0.05
PAAD	chr19	36099445	Missense_Mutation	novel	R856H	0.17
PCPG	chr19	36094121	Silent	novel	P808P	0.09
PRAD	chr19	36091276	Missense_Mutation	rs750547223	S704L	0.09
PRAD	chr19	36103198	Missense_Mutation	rs771467789	R1164C	0.2
PRAD	chr19	36103530	Silent	rs143638774	L1229L	0.31
READ	chr19	36083226	Missense_Mutation	rs375417358	R512Q	0.26
READ	chr19	36090510	Missense_Mutation	NA	S675F	0.33
READ	chr19	36084678	Missense_Mutation	rs147875659	E526K	0.35
SARC	chr19	36103551	Silent	rs775723707	I1236I	0.43
SKCM	chr19	36066381	Missense_Mutation	NA	S172F	0.26
SKCM	chr19	36071682	Missense_Mutation	NA	L337F	0.25
SKCM	chr19	36099494	Silent	novel	P872P	0.44
SKCM	chr19	36099452	Silent	NA	Y858Y	0.22
SKCM	chr19	36103526	Missense_Mutation	novel	S1228F	0.08
SKCM	chr19	36103527	Silent	novel	S1228S	0.07
SKCM	chr19	36060101	Intron	novel		0.21
SKCM	chr19	36100789	Silent	NA	F927F	0.22
SKCM	chr19	36102077	Missense_Mutation	NA	S1049F	0.32
SKCM	chr19	36090511	Silent	NA	S675S	0.46
SKCM	chr19	36103023	Silent	rs765013257	G1132G	0.44
SKCM	chr19	36103531	Missense_Mutation	rs771618020	G1230S	0.52
SKCM	chr19	36102108	Silent	NA	F1059F	0.27
SKCM	chr19	36091226	Silent	NA	F687F	0.33
SKCM	chr19	36092716	Silent	rs190314006	P746P	0.15
SKCM	chr19	36067867	Silent	NA	L247L	0.16
SKCM	chr19	36083127	Missense_Mutation	NA	P479L	0.19
SKCM	chr19	36084657	Missense_Mutation	NA	H519Y	0.44
SKCM	chr19	36100786	Silent	NA	S926S	0.37
SKCM	chr19	36084657	Missense_Mutation	NA	H519Y	0.41
SKCM	chr19	36097032	Missense_Mutation	NA	R825C	0.18
SKCM	chr19	36086715	Silent	novel	R557R	0.25
SKCM	chr19	36081569	Missense_Mutation	NA	N457S	0.38
SKCM	chr19	36091456	Missense_Mutation	NA	S734F	0.1
SKCM	chr19	36104587	Missense_Mutation	rs768909004	P1403L	0.4
SKCM	chr19	36101308	Missense_Mutation	NA	P988S	0.57
SKCM	chr19	36067839	Silent	NA	T237T	0.25
SKCM	chr19	36081439	Missense_Mutation	NA	P414S	0.39
STAD	chr19	36103586	Missense_Mutation	rs778175384	S1248L	0.32
STAD	chr19	36104993	Missense_Mutation	NA	V1508L	0.62
STAD	chr19	36103382	Missense_Mutation	NA	S1180F	0.17
STAD	chr19	36066005	Missense_Mutation	novel	V127A	0.36
STAD	chr19	36073516	Silent	rs766269117	Y406Y	0.33
STAD	chr19	36102018	Silent	rs141344823	C1029C	0.12
STAD	chr19	36103076	Splice_Site	novel	X1149_splice	0.46
STAD	chr19	36084746	Splice_Site	NA	X548_splice	0.14
STAD	chr19	36067315	Missense_Mutation	rs768099287	V191I	0.27
STAD	chr19	36067436	Missense_Mutation	NA	E231G	0.3
STAD	chr19	36104928	Missense_Mutation	rs542711912	P1486L	0.31
STAD	chr19	36089092	Missense_Mutation	rs774588484	R608H	0.45
STAD	chr19	36099465	Missense_Mutation	rs764299399	R863C	0.15
STAD	chr19	36103058	Missense_Mutation	novel	S1144F	0.35
STAD	chr19	36092780	Missense_Mutation	rs532692601	T768A	0.13
STAD	chr19	36067955	Missense_Mutation	NA	G276A	0.22
STAD	chr19	36091240	Missense_Mutation	NA	C692Y	0.19
STAD	chr19	36103552	Missense_Mutation	rs143493857	V1237M	0.13
STAD	chr19	36066358	Silent	NA	S164S	0.21
STAD	chr19	36103709	Missense_Mutation	rs773029330	R1289Q	0.19
STAD	chr19	36092692	Silent	rs757339378	C738C	0.29
STAD	chr19	36060216	Intron	novel		0.33
STAD	chr19	36073421	Missense_Mutation	NA	S375T	0.3
STAD	chr19	36103973	Missense_Mutation	novel	P1377L	0.15
STAD	chr19	36104844	Missense_Mutation	novel	H1458R	0.53
STAD	chr19	36103173	Missense_Mutation	NA	K1155N	0.41
STAD	chr19	36104670	Missense_Mutation	rs756795208	R1431C	0.19
STAD	chr19	36103825	Nonsense_Mutation	novel	E1328*	0.09
STAD	chr19	36092795	Missense_Mutation	NA	R773W	0.15
STAD	chr19	36103862	Missense_Mutation	rs774129490	R1340H	0.24
TGCT	chr19	36091260	Missense_Mutation	novel	V699M	0.11
THCA	chr19	36067990	Nonsense_Mutation	NA	E288*	0.14
THYM	chr19	36067435	Missense_Mutation	novel	E231K	0.26
UCEC	chr19	36103552	Missense_Mutation	rs143493857	V1237M	0.38
UCEC	chr19	36091453	Missense_Mutation	novel	V733A	0.12
UCEC	chr19	36101715	Missense_Mutation	novel	S1008F	0.22
UCEC	chr19	36103373	Missense_Mutation	novel	V1177A	0.34
UCEC	chr19	36067926	Silent	rs777355565	A266A	0.34
UCEC	chr19	36104670	Missense_Mutation	rs756795208	R1431C	0.38
UCEC	chr19	36071555	Splice_Site	novel	X295_splice	0.39
UCEC	chr19	36101745	Missense_Mutation	NA	R1018Q	0.56
UCEC	chr19	36068012	Splice_Site	novel	X294_splice	0.41
UCEC	chr19	36099443	Silent	novel	K855K	0.5
UCEC	chr19	36104828	Missense_Mutation	novel	T1453A	0.32
UCEC	chr19	36066278	Missense_Mutation	rs369843158	R138C	0.48
UCEC	chr19	36103488	Silent	novel	A1215A	0.36
UCEC	chr19	36105079	3'UTR	novel		0.33
UCEC	chr19	36099552	Missense_Mutation	NA	E892K	0.28
UCEC	chr19	36067855	Missense_Mutation	NA	R243C	0.24
UCEC	chr19	36101306	Missense_Mutation	NA	S987N	0.43
UCEC	chr19	36103023	Silent	rs765013257	G1132G	0.11
UCEC	chr19	36103451	Missense_Mutation	novel	G1203D	0.08
UCEC	chr19	36067843	Missense_Mutation	NA	P239S	0.23
UCEC	chr19	36104607	Missense_Mutation	NA	S1410G	0.44
UCEC	chr19	36067967	Missense_Mutation	novel	Q280R	0.36
UCEC	chr19	36083226	Missense_Mutation	rs375417358	R512Q	0.39
UCEC	chr19	36099615	Nonsense_Mutation	novel	E913*	0.42
UCEC	chr19	36103692	Missense_Mutation	novel	W1283C	0.35
UCEC	chr19	36086784	Silent	novel	S580S	0.24
UCEC	chr19	36101309	Missense_Mutation	rs753553053	P988L	0.24
UCEC	chr19	36104873	Missense_Mutation	NA	G1468R	0.17
UCEC	chr19	36101259	Silent	NA	Q971Q	0.18
UCEC	chr19	36073476	Missense_Mutation	novel	R393I	0.35
UCEC	chr19	36104520	Missense_Mutation	novel	A1381T	0.58
UCEC	chr19	36073360	Missense_Mutation	NA	K354N	0.22
UCEC	chr19	36102747	Splice_Region	rs187029707		0.48
UCEC	chr19	36054983	Silent	NA	V4V	0.36
UCEC	chr19	36091405	Missense_Mutation	novel	I717S	0.09
UCEC	chr19	36099500	Silent	NA	K874K	0.24
UCEC	chr19	36091276	Missense_Mutation	rs750547223	S704L	0.3
UCEC	chr19	36066332	Missense_Mutation	novel	Y156H	0.33
UCEC	chr19	36073386	Missense_Mutation	novel	V363A	0.35
UCEC	chr19	36103074	Splice_Region	novel	H1149H	0.38
UCEC	chr19	36066279	Missense_Mutation	rs199673795	R138H	0.48
UCEC	chr19	36083170	Silent	rs150656878	A493A	0.4
UCEC	chr19	36101770	Missense_Mutation	novel	F1026L	0.33
UCEC	chr19	36090463	Silent	rs79238222	N659N	0.57
UCEC	chr19	36081561	Silent	novel	I454I	0.28
UCEC	chr19	36104899	Silent	novel	A1476A	0.31
UCEC	chr19	36073432	Nonsense_Mutation	novel	Y378*	0.45
UCEC	chr19	36102113	Missense_Mutation	rs150778662	R1061H	0.5
UCEC	chr19	36103024	Missense_Mutation	rs750117864	G1133R	0.35
UCEC	chr19	36103356	Silent	rs762202259	T1171T	0.6
UCEC	chr19	36094092	Nonsense_Mutation	novel	E799*	0.08
UCEC	chr19	36058849	Missense_Mutation	novel	G83C	0.36
UCEC	chr19	36101725	Silent	rs118175551	P1011P	0.33
UCEC	chr19	36091280	Silent	NA	G705G	0.23
UCEC	chr19	36094039	Missense_Mutation	rs372603166	T781M	0.42
UCEC	chr19	36090520	Splice_Region	novel	K678K	0.52
UCEC	chr19	36060166	Intron	novel		0.07
UCEC	chr19	36060168	Intron	novel		0.05
UCEC	chr19	36092806	Frame_Shift_Del	novel	*R778Gfs15**	0.38
UCEC	chr19	36055054	Missense_Mutation	novel	R28L	0.68
UCEC	chr19	36055074	Frame_Shift_Del	novel	*A37Pfs40**	0.5
UCEC	chr19	36100772	Missense_Mutation	rs151119220	R922C	0.32
UCEC	chr19	36104938	Frame_Shift_Del	novel	*L1491Wfs41**	0.75
UCEC	chr19	36092704	Nonsense_Mutation	novel	W742*	0.19
UCEC	chr19	36102064	Missense_Mutation	rs563536911	V1045I	0.42
UCEC	chr19	36103955	Missense_Mutation	novel	T1371N	0.18
UCEC	chr19	36089083	Missense_Mutation	novel	I605T	0.5
UCEC	chr19	36089085	Missense_Mutation	NA	Y606H	0.43
UCEC	chr19	36073443	Missense_Mutation	NA	S382I	0.24
UCEC	chr19	36083074	Missense_Mutation	NA	K461N	0.33
UCEC	chr19	36089091	Missense_Mutation	rs553327137	R608C	0.35
UCEC	chr19	36100817	Missense_Mutation	novel	A937T	0.36
UCEC	chr19	36094071	Silent	novel	L792L	0.39
UCEC	chr19	36086769	Silent	novel	T575T	0.48
UCEC	chr19	36104581	Missense_Mutation	novel	A1401V	0.35
UCS	chr19	36083152	Silent	novel	T487T	0.21
UCS	chr19	36100775	Missense_Mutation	rs141094124	G923R	0.16

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
READ	DEL	0.0303	0.23023

Survival Analysis

Cancer	P-value	Q-value
THYM	0.0074	Kaplan-Meier Survival Analysis
KIRC	0.00011	Kaplan-Meier Survival Analysis
STAD	0.013	Kaplan-Meier Survival Analysis
MESO	0.00014	Kaplan-Meier Survival Analysis
ACC	0.00012	Kaplan-Meier Survival Analysis
HNSC	0.016	Kaplan-Meier Survival Analysis
SKCM	0.0001	Kaplan-Meier Survival Analysis
LUSC	0.048	Kaplan-Meier Survival Analysis
KIRP	0.0001	Kaplan-Meier Survival Analysis
CESC	0.0048	Kaplan-Meier Survival Analysis
UCEC	0.026	Kaplan-Meier Survival Analysis
LIHC	0.0001	Kaplan-Meier Survival Analysis
DLBC	0.0036	Kaplan-Meier Survival Analysis
LUAD	0.0024	Kaplan-Meier Survival Analysis
UVM	0.0093	Kaplan-Meier Survival Analysis
OV	0.028	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: ENSG00000075702 (Gene tree)
Gene ID: 284403
Gene Symbol: WDR62
Alias: DKFZP434J046|FLJ33298|C19orf14|MCPH2
Full Name: WD repeat domain 62
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Plus strand
Length: 50,231 bases
Position: chr19:36,054,881-36,105,111
Accession: 24502
RBP type: non-canonical RBP
Summary: This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2011]

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
ENST00000270301	WDR62-201	4632	-	ENSP00000270301	1518 (aa)	-	O43379
ENST00000608676	WDR62-207	2960	-	-	- (aa)	-	-
ENST00000401500	WDR62-203	4682	XM_005258809	ENSP00000384792	1523 (aa)	XP_005258866	O43379
ENST00000378860	WDR62-202	1980	-	-	- (aa)	-	-
ENST00000587391	WDR62-205	5971	-	ENSP00000465525	483 (aa)	-	O43379
ENST00000644764	WDR62-208	1418	-	ENSP00000494253	347 (aa)	-	A0A2R8YD43
ENST00000427823	WDR62-204	955	-	ENSP00000413475	318 (aa)	-	H7C3R4
ENST00000589953	WDR62-206	664	-	-	- (aa)	-	-

Gene Model

Click here to download ENSG00000075702's gene model file

Phenotypes

ensgID	Trait	pValue	Pubmed ID
ENSG00000075702	Hypertension	1.7292077E-006	-

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000075702's network

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

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0000922	spindle pole	21873635.	IBA	Component
GO:0000922	spindle pole	20890278.20890279.	IDA	Component
GO:0005515	protein binding	16189514.25416956.26297806.26496610.28089251.	IPI	Function
GO:0005634	nucleus	21873635.	IBA	Component
GO:0005634	nucleus	20729831.	IDA	Component
GO:0005813	centrosome	26297806.	IDA	Component
GO:0005814	centriole	-	IEA	Component
GO:0005815	microtubule organizing center	-	IDA	Component
GO:0005829	cytosol	-	IDA	Component
GO:0007052	mitotic spindle organization	21873635.	IBA	Process
GO:0007052	mitotic spindle organization	24388750.	IMP	Process
GO:0007099	centriole replication	26297806.	IMP	Process
GO:0021987	cerebral cortex development	20729831.	IMP	Process
GO:0022008	neurogenesis	21873635.	IBA	Process
GO:0022008	neurogenesis	20890278.	IMP	Process

EuRBPDB

Note: to get the extension of tumor abbreviations.

Select Dataset :

Input Drug :

Input Cell Line :

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.