EuRBPDB

Basic Information
Cancer Related Information

Description

RBPome

Expression

Transcripts

Gene Model

GWAS

PPI

Gene Ontology

Description

Ensembl ID: ENSG00000076201 (Gene tree)
Gene ID: 25930
Gene Symbol: PTPN23
Alias: DKFZP564F0923|KIAA1471|HD-PTP
Full Name: protein tyrosine phosphatase non-receptor type 23
Gene Type: protein_coding
Species: Homo_sapiens
Status: putative
Strand: Plus strand
Length: 32,460 bases
Position: chr3:47,380,982-47,413,441
Accession: 14406
RBP type: non-canonical RBP
Summary: This gene encodes a member of the non-receptor type protein-tyrosine phosphatase family. The encoded protein may be involved in the regulation of small nuclear ribonucleo protein assembly and pre-mRNA splicing by modifying the survival motor neuron (SMN) complex. The encoded protein additionally plays a role in ciliogenesis and is part of endosomal sorting complex required for transport (ESCRT) pathways. This gene may serve a tumor suppressor function. [provided by RefSeq, Jul 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 & MCF10A	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
ENST00000456221	PTPN23-202	592	-	ENSP00000396328	169 (aa)	-	C9JD91
ENST00000477276	PTPN23-204	882	-	-	- (aa)	-	-
ENST00000495653	PTPN23-205	676	-	-	- (aa)	-	-
ENST00000462998	PTPN23-203	260	-	-	- (aa)	-	-
ENST00000602307	PTPN23-206	5119	-	ENSP00000473266	64 (aa)	-	R4GMM7
ENST00000265562	PTPN23-201	5244	XM_005265031	ENSP00000265562	1636 (aa)	XP_005265088	Q9H3S7

Gene Model

Click here to download ENSG00000076201's gene model file

GWAS

ensgID	SNP	Chromosome	Position	SNP-risk	Trait	PubmedID	95% CI	Or or BEAT	EFO ID
ENSG00000076201	rs6780013	3	47410628	G	Type 2 diabetes (adjusted for BMI)	29632382	[1.02-1.05]	1.03	EFO_0001360

Protein-Protein Interaction (PPI)

Clik here to download ENSG00000076201's network

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

Gene Ontology

Go ID	Go_term	PubmedID	Evidence	Category
GO:0004725	protein tyrosine phosphatase activity	21724833.	IMP	Function
GO:0005515	protein binding	17174262.18434552.18835089.19523899.20936779.21179510.21724833.25416956.	IPI	Function
GO:0005634	nucleus	21179510.	IDA	Component
GO:0005654	nucleoplasm	-	IDA	Component
GO:0005654	nucleoplasm	-	TAS	Component
GO:0005737	cytoplasm	21179510.	IDA	Component
GO:0005768	endosome	21179510.	IDA	Component
GO:0005769	early endosome	21757351.	IDA	Component
GO:0005829	cytosol	-	IEA	Component
GO:0010633	negative regulation of epithelial cell migration	21724833.	IMP	Process
GO:0015031	protein transport	-	IEA	Process
GO:0016604	nuclear body	-	IDA	Component
GO:0019901	protein kinase binding	21724833.	IPI	Function
GO:0032456	endocytic recycling	24821423.	IMP	Process
GO:0035335	peptidyl-tyrosine dephosphorylation	-	IEA	Process
GO:0036064	ciliary basal body	20393563.	IDA	Component
GO:0043162	ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway	21757351.	IMP	Process
GO:0045022	early endosome to late endosome transport	24821423.	IMP	Process
GO:0060271	cilium assembly	20393563.	IMP	Process
GO:0061357	positive regulation of Wnt protein secretion	24821423.	IMP	Process
GO:0070062	extracellular exosome	19056867.	HDA	Component
GO:0071345	cellular response to cytokine stimulus	-	TAS	Process
GO:1903387	positive regulation of homophilic cell adhesion	21724833.	IMP	Process
GO:1903393	positive regulation of adherens junction organization	21724833.	IMP	Process
GO:2000643	positive regulation of early endosome to late endosome transport	21724833.	IMP	Process

Cancer associated literatures

PID	Title	Article	Time	Author	Doi
21724833	Identification of PTPN23 as a novel regulator of cell invasion in mammary epithelial cells from a loss-of-function screen of the 'PTP-ome'.	Genes Dev	2011 Jul 1	Lin G	doi: 10.1101/gad.2018911.
27210750	Haploinsufficiency of the ESCRT Component HD-PTP Predisposes to Cancer.	Cell Rep	2016 May 31	Manteghi S	doi: 10.1016/j.celrep.2016.04.076
23843459	Tumor-suppressive function of protein-tyrosine phosphatase non-receptor type 23 in testicular germ cell tumors is lost upon overexpression of miR142-3p microRNA.	J Biol Chem	2013 Aug 16	Tanaka K	doi: 10.1074/jbc.M113.478891
19340315	HD-PTP is a catalytically inactive tyrosine phosphatase due to a conserved divergence in its phosphatase domain.	PLoS One	2009	Gingras MC	doi: 10.1371/journal.pone.0005105
28620046	Role of ESCRT component HD-PTP/PTPN23 in cancer.	Biochem Soc Trans	2017 Jun 15	Gingras MC	doi: 10.1042/BST20160332.

Expression in 33 cancers

Mutations

Cancer	Chr	Position	Mutation Type	dbSNP	Protein-change	Allele Freq
ACC	chr3	47412153	Missense_Mutation	novel	Y1378C	0.91
BLCA	chr3	47408975	Silent	NA	F510F	0.21
BLCA	chr3	47405054	Missense_Mutation	NA	E113K	0.24
BLCA	chr3	47406349	Missense_Mutation	novel	E191Q	0.1
BLCA	chr3	47405962	Silent	rs772744440	F154F	0.23
BLCA	chr3	47406553	In_Frame_Del	novel	Q234_W237del	0.34
BRCA	chr3	47411507	Missense_Mutation	rs755103681	R1237C	0.13
BRCA	chr3	47407760	Missense_Mutation	novel	I356T	0.21
BRCA	chr3	47409964	Silent	NA	A722A	0.24
BRCA	chr3	47412513	Splice_Site	novel	X1440_splice	0.15
BRCA	chr3	47409278	In_Frame_Del	novel	A588_T593del	0.19
BRCA	chr3	47409476	Silent	NA	N619N	0.37
BRCA	chr3	47411408	Missense_Mutation	novel	H1204D	0.32
BRCA	chr3	47409692	Missense_Mutation	NA	E663K	0.21
BRCA	chr3	47412341	Nonsense_Mutation	NA	E1413*	0.27
BRCA	chr3	47409964	Silent	novel	A722A	0.24
BRCA	chr3	47409695	Missense_Mutation	NA	A664P	0.52
BRCA	chr3	47409054	Missense_Mutation	rs746807105	R537W	0.45
CESC	chr3	47412564	Silent	rs756230136	V1456V	0.45
CESC	chr3	47409709	Silent	NA	L668L	0.34
CESC	chr3	47413290	3'UTR	novel		0.15
CESC	chr3	47413292	3'UTR	novel		0.17
CESC	chr3	47409024	Missense_Mutation	rs150002416	R527C	0.26
CESC	chr3	47409836	Splice_Site	novel	X710_splice	0.23
CESC	chr3	47405936	Missense_Mutation	NA	H146Y	0.34
CESC	chr3	47408444	Silent	NA	L428L	0.57
COAD	chr3	47404683	Missense_Mutation	NA	G64D	0.37
COAD	chr3	47409444	Frame_Shift_Del	novel	Y609*	0.31
COAD	chr3	47405928	Missense_Mutation	NA	S143F	0.38
COAD	chr3	47404753	Silent	NA	G87G	0.36
COAD	chr3	47381078	5'UTR	novel		0.35
COAD	chr3	47410785	Frame_Shift_Del	NA	*Y998Tfs162**	0.34
COAD	chr3	47412943	Nonsense_Mutation	NA	Q1557*	0.33
COAD	chr3	47410253	Missense_Mutation	NA	P819S	0.35
COAD	chr3	47412805	Frame_Shift_Del	novel	*L1513Wfs71**	0.44
COAD	chr3	47410325	Missense_Mutation	rs139305961	V843M	0.39
COAD	chr3	47411872	Silent	rs201197775	T1326T	0.23
COAD	chr3	47408994	Missense_Mutation	rs775291877	R517C	0.26
COAD	chr3	47411518	Missense_Mutation	NA	K1240N	0.35
COAD	chr3	47409530	Silent	rs778078873	Y637Y	0.14
COAD	chr3	47410831	Frame_Shift_Ins	rs770411657	*L1014Pfs68**	0.36
COAD	chr3	47412921	Silent	NA	S1549S	0.13
COAD	chr3	47396201	Missense_Mutation	novel	L48P	0.07
COAD	chr3	47408430	Nonsense_Mutation	novel	K424*	0.15
COAD	chr3	47410042	Frame_Shift_Del	NA	*P750Lfs53**	0.06
COAD	chr3	47411566	Frame_Shift_Del	novel	*P1258Rfs2**	0.28
COAD	chr3	47411507	Missense_Mutation	rs755103681	R1237C	0.32
COAD	chr3	47410042	Frame_Shift_Del	NA	*P750Lfs53**	0.05
COAD	chr3	47413000	Missense_Mutation	NA	S1576P	0.12
ESCA	chr3	47408351	Missense_Mutation	novel	F397L	0.2
ESCA	chr3	47413084	Missense_Mutation	novel	N1604H	0.23
ESCA	chr3	47411305	Missense_Mutation	novel	E1169D	0.35
GBM	chr3	47405030	Missense_Mutation	novel	V105M	0.21
GBM	chr3	47405752	Missense_Mutation	novel	A123G	0.88
GBM	chr3	47407328	Missense_Mutation	novel	Q295P	0.12
GBM	chr3	47406365	Missense_Mutation	novel	D196G	0.48
HNSC	chr3	47409428	Silent	novel	E603E	0.07
HNSC	chr3	47409173	Silent	rs141629698	A551A	0.31
HNSC	chr3	47406603	Silent	novel	A250A	0.26
HNSC	chr3	47409505	Missense_Mutation	rs780485797	A629V	0.87
HNSC	chr3	47410025	Missense_Mutation	novel	E743K	0.59
HNSC	chr3	47411677	Missense_Mutation	novel	E1293D	0.13
KIRC	chr3	47411320	Silent	NA	L1174L	0.4
KIRP	chr3	47410827	Missense_Mutation	novel	P1010R	0.25
LAML	chr3	47409075	Missense_Mutation	novel	A544T	0.12
LGG	chr3	47405947	Nonsense_Mutation	NA	C149*	0.09
LGG	chr3	47408937	Missense_Mutation	novel	W498R	0.36
LGG	chr3	47409253	Missense_Mutation	rs754253770	R578H	0.3
LIHC	chr3	47410566	Missense_Mutation	NA	T923I	0.31
LIHC	chr3	47410042	Frame_Shift_Del	NA	*P750Lfs53**	0.1
LIHC	chr3	47407696	Splice_Site	NA	X335_splice	0.59
LIHC	chr3	47413310	3'UTR	novel		0.3
LIHC	chr3	47411886	Missense_Mutation	rs754079072	E1331V	0.42
LUAD	chr3	47411141	Missense_Mutation	rs763104053	A1115T	0.22
LUAD	chr3	47412353	Missense_Mutation	rs773663848	G1417R	0.23
LUAD	chr3	47407767	Silent	rs781110452	A358A	0.15
LUAD	chr3	47409697	Silent	rs752849441	A664A	0.26
LUAD	chr3	47408796	Missense_Mutation	NA	D451N	0.2
LUAD	chr3	47413104	Missense_Mutation	novel	N1610K	0.3
LUAD	chr3	47413105	Missense_Mutation	novel	G1611W	0.3
LUAD	chr3	47409540	Missense_Mutation	novel	R641W	0.28
LUAD	chr3	47405972	Silent	novel	R158R	0.46
LUSC	chr3	47411007	Missense_Mutation	rs762143288	R1070Q	0.16
LUSC	chr3	47407931	Missense_Mutation	novel	I387S	0.17
LUSC	chr3	47408435	Silent	rs775178936	C425C	0.58
OV	chr3	47412295	Frame_Shift_Ins	novel	*R1398Cfs54**	0.11
OV	chr3	47411565	Frame_Shift_Ins	rs758419807	*L1259Afs14**	0.14
OV	chr3	47408975	Silent	NA	F510F	0.27
OV	chr3	47407185	Missense_Mutation	novel	K288R	0.14
PAAD	chr3	47411196	Missense_Mutation	novel	S1133F	0.23
PAAD	chr3	47408344	Splice_Site	novel	X395_splice	0.15
PAAD	chr3	47410459	Silent	novel	I887I	0.13
PAAD	chr3	47412960	Silent	rs371856828	P1562P	0.14
PAAD	chr3	47413027	Missense_Mutation	novel	P1585T	0.18
PRAD	chr3	47412594	Missense_Mutation	novel	C1466W	0.24
PRAD	chr3	47396145	Splice_Region	novel	F29F	0.1
PRAD	chr3	47408993	Silent	rs151244361	H516H	0.1
READ	chr3	47407761	Silent	NA	I356I	0.22
READ	chr3	47412146	Missense_Mutation	rs749890466	A1376T	0.24
READ	chr3	47411006	Nonsense_Mutation	rs767454205	R1070*	0.3
READ	chr3	47411198	Missense_Mutation	NA	P1134S	0.58
SARC	chr3	47409434	Missense_Mutation	novel	Q605H	0.07
SKCM	chr3	47411345	Missense_Mutation	NA	G1183S	0.31
SKCM	chr3	47411476	Silent	rs763493430	V1226V	0.23
SKCM	chr3	47413134	In_Frame_Del	novel	D1622del	0.29
SKCM	chr3	47412130	Silent	NA	F1370F	0.35
SKCM	chr3	47413110	Missense_Mutation	novel	Q1612H	0.32
SKCM	chr3	47411822	Missense_Mutation	novel	P1310S	0.66
SKCM	chr3	47411823	Missense_Mutation	novel	P1310L	0.67
SKCM	chr3	47407912	Missense_Mutation	novel	R381W	0.37
SKCM	chr3	47407933	Missense_Mutation	novel	E388K	0.44
SKCM	chr3	47408397	Missense_Mutation	NA	A413T	0.46
SKCM	chr3	47412166	Silent	NA	R1382R	0.29
SKCM	chr3	47406382	Silent	NA	L202L	0.45
SKCM	chr3	47412739	Missense_Mutation	NA	L1489F	0.48
SKCM	chr3	47410193	Missense_Mutation	NA	P799S	0.54
SKCM	chr3	47412168	Missense_Mutation	NA	P1383R	0.23
STAD	chr3	47412300	Missense_Mutation	NA	T1399M	0.37
STAD	chr3	47407333	Missense_Mutation	rs750641394	A297T	0.31
STAD	chr3	47411098	Frame_Shift_Del	NA	*P1102Qfs58**	0.39
STAD	chr3	47411141	Missense_Mutation	rs763104053	A1115T	0.25
STAD	chr3	47406012	Missense_Mutation	rs780215762	R171H	0.29
STAD	chr3	47411861	Missense_Mutation	rs778612238	V1323I	0.29
STAD	chr3	47410042	Frame_Shift_Del	NA	*P750Lfs53**	0.44
STAD	chr3	47412991	Frame_Shift_Ins	novel	*P1573Lfs32**	0.45
STAD	chr3	47405974	Silent	novel	R158R	0.52
STAD	chr3	47410832	Frame_Shift_Del	NA	*L1014Yfs146**	0.23
STAD	chr3	47410042	Frame_Shift_Del	NA	*P750Lfs53**	0.75
STAD	chr3	47412623	In_Frame_Del	rs766407272	K1477del	0.33
STAD	chr3	47408460	Missense_Mutation	novel	T434A	0.11
STAD	chr3	47409181	Missense_Mutation	novel	Q554P	0.11
STAD	chr3	47407556	Silent	novel	P325P	0.23
STAD	chr3	47405785	Missense_Mutation	NA	R134Q	0.19
STAD	chr3	47408456	Silent	rs756391820	P432P	0.17
STAD	chr3	47409060	Missense_Mutation	NA	A539T	0.33
STAD	chr3	47409228	Missense_Mutation	rs765847614	R570C	0.08
STAD	chr3	47409557	Silent	NA	D646D	0.38
STAD	chr3	47412414	In_Frame_Del	rs760387665	E1438del	0.14
STAD	chr3	47409816	Missense_Mutation	NA	R704H	0.25
STAD	chr3	47411098	Frame_Shift_Del	NA	*P1102Qfs58**	0.48
STAD	chr3	47406491	Missense_Mutation	NA	Y213C	0.09
STAD	chr3	47410318	Silent	novel	Q840Q	0.24
STAD	chr3	47412402	Missense_Mutation	NA	K1433M	0.34
STAD	chr3	47409192	Missense_Mutation	NA	R558C	0.17
STAD	chr3	47408411	Silent	NA	I417I	0.26
STAD	chr3	47411796	Missense_Mutation	rs573090718	R1301H	0.07
STAD	chr3	47410832	Frame_Shift_Del	NA	*L1014Yfs146**	0.11
STAD	chr3	47412126	Missense_Mutation	rs201950738	R1369H	0.18
STAD	chr3	47410832	Frame_Shift_Del	NA	*L1014Yfs146**	0.46
STAD	chr3	47411166	Missense_Mutation	novel	S1123I	0.48
TGCT	chr3	47409060	Missense_Mutation	novel	A539P	0.33
UCEC	chr3	47408924	Missense_Mutation	NA	E493D	0.52
UCEC	chr3	47396188	Nonsense_Mutation	NA	E44*	0.3
UCEC	chr3	47408932	Missense_Mutation	NA	R496Q	0.35
UCEC	chr3	47409438	Missense_Mutation	NA	K607E	0.26
UCEC	chr3	47396175	Missense_Mutation	novel	E39D	0.14
UCEC	chr3	47405766	Silent	novel	L128L	0.43
UCEC	chr3	47408360	Silent	novel	S400S	0.38
UCEC	chr3	47408826	Missense_Mutation	novel	D461Y	0.41
UCEC	chr3	47407149	Missense_Mutation	novel	A276V	0.11
UCEC	chr3	47412146	Missense_Mutation	rs749890466	A1376T	0.33
UCEC	chr3	47409024	Missense_Mutation	rs150002416	R527C	0.34
UCEC	chr3	47409299	Silent	novel	T593T	0.34
UCEC	chr3	47396200	Missense_Mutation	novel	L48M	0.44
UCEC	chr3	47404698	Missense_Mutation	rs367969329	R69H	0.48
UCEC	chr3	47410094	Missense_Mutation	novel	A766S	0.33
UCEC	chr3	47405767	Missense_Mutation	novel	L128R	0.46
UCEC	chr3	47405957	Missense_Mutation	rs370113013	A153T	0.41
UCEC	chr3	47407340	Missense_Mutation	rs201653035	R299H	0.35
UCEC	chr3	47407935	Missense_Mutation	NA	E388D	0.12
UCEC	chr3	47412974	Missense_Mutation	NA	A1567V	0.18
UCEC	chr3	47406525	Silent	rs375545134	P224P	0.14
UCEC	chr3	47408785	Missense_Mutation	rs755297831	G447D	0.17
UCEC	chr3	47409816	Missense_Mutation	NA	R704H	0.25
UCEC	chr3	47406732	Silent	NA	Q263Q	0.14
UCEC	chr3	47406597	Silent	rs371725325	F248F	0.36
UCEC	chr3	47408994	Missense_Mutation	rs775291877	R517C	0.26
UCEC	chr3	47409817	Silent	novel	R704R	0.25
UCEC	chr3	47410283	Missense_Mutation	novel	P829S	0.21
UCEC	chr3	47411946	Missense_Mutation	rs770830112	H1351R	0.38
UCEC	chr3	47412819	Silent	novel	S1515S	0.41
UCEC	chr3	47409248	Silent	novel	Q576Q	0.35
UCEC	chr3	47406044	Splice_Region	novel	L182L	0.27
UCEC	chr3	47381124	Missense_Mutation	novel	I10V	0.31
UCEC	chr3	47409811	Silent	novel	A702A	0.41
UCEC	chr3	47409075	Missense_Mutation	novel	A544T	0.53
UCEC	chr3	47409937	Missense_Mutation	novel	K713N	0.44
UCEC	chr3	47409438	Frame_Shift_Del	novel	*K608Sfs5**	0.37
UCEC	chr3	47405997	Missense_Mutation	novel	S166N	0.08
UCEC	chr3	47412910	Missense_Mutation	rs538249359	P1546T	0.45
UCEC	chr3	47410495	Silent	novel	P899P	0.22
UCEC	chr3	47407525	In_Frame_Del	novel	N316del	0.44
UCEC	chr3	47412805	Frame_Shift_Del	novel	*L1513Wfs71**	0.49
UCEC	chr3	47409543	Missense_Mutation	novel	R642W	0.42
UCEC	chr3	47411890	Silent	rs765250574	R1332R	0.39
UCEC	chr3	47411657	Missense_Mutation	novel	M1287V	0.14
UCEC	chr3	47412300	Missense_Mutation	NA	T1399M	0.25
UCEC	chr3	47408435	Silent	rs775178936	C425C	0.44
UCEC	chr3	47409002	Missense_Mutation	novel	M519I	0.38
UCEC	chr3	47408358	Missense_Mutation	novel	S400A	0.09
UCEC	chr3	47412798	Silent	rs776628485	R1508R	0.42
UCEC	chr3	47413205	3'UTR	novel		0.41
UCEC	chr3	47410042	Frame_Shift_Del	NA	*P750Lfs53**	0.37
UCEC	chr3	47404763	Missense_Mutation	rs760010594	A91T	0.35
UCEC	chr3	47408436	Missense_Mutation	rs760349861	A426T	0.27
UCEC	chr3	47410042	Frame_Shift_Del	NA	*P750Lfs53**	0.08
UCEC	chr3	47410172	Frame_Shift_Del	novel	*P793Lfs10**	0.36
UCEC	chr3	47413012	Silent	novel	L1580L	0.31
UCEC	chr3	47410220	Missense_Mutation	novel	P808T	0.51
UCEC	chr3	47411222	Nonsense_Mutation	novel	Q1142*	0.42
UCEC	chr3	47407340	Missense_Mutation	rs201653035	R299H	0.36
UCEC	chr3	47411899	Silent	novel	S1335S	0.52
UCEC	chr3	47405011	Missense_Mutation	novel	E98D	0.22
UCEC	chr3	47405947	Silent	rs747539038	C149C	0.67
UCEC	chr3	47407530	Missense_Mutation	rs768465983	D317N	0.47
UCEC	chr3	47409540	Missense_Mutation	novel	R641W	0.33
UCEC	chr3	47412125	Missense_Mutation	NA	R1369C	0.23
UCEC	chr3	47412993	Silent	novel	P1573P	0.67
UCEC	chr3	47409480	Missense_Mutation	novel	A621T	0.36
UCEC	chr3	47407160	Missense_Mutation	novel	L280F	0.28
UCEC	chr3	47409197	Silent	novel	I559I	0.37
UCS	chr3	47410067	Nonsense_Mutation	novel	R757*	0.18
UCS	chr3	47410941	Missense_Mutation	novel	P1048R	0.46
UVM	chr3	47412576	Silent	novel	H1460H	0.8

Copy Number Variations (CNVs)

Cancer	Type	Freq	Q-value
CHOL	DEL	0.8056	0.02241
DLBC	DEL	0.1458	0.016959
GBM	DEL	0.078	0.056565
LGG	DEL	0.0858	0.00089193
LUAD	DEL	0.3391	0.0021265
PAAD	DEL	0.1902	0.030662
SARC	DEL	0.2023	0.0034746
SKCM	DEL	0.1635	0.13887
TGCT	DEL	0.2	0.08422
THYM	DEL	0.0976	0.037527

Survival Analysis

Cancer	P-value	Q-value
SARC	0.0017	Kaplan-Meier Survival Analysis
HNSC	0.0023	Kaplan-Meier Survival Analysis
SKCM	0.00085	Kaplan-Meier Survival Analysis
PRAD	0.044	Kaplan-Meier Survival Analysis
BRCA	0.0018	Kaplan-Meier Survival Analysis
KICH	0.012	Kaplan-Meier Survival Analysis
LIHC	0.0026	Kaplan-Meier Survival Analysis
LGG	0.0017	Kaplan-Meier Survival Analysis
THCA	0.04	Kaplan-Meier Survival Analysis
LUAD	0.048	Kaplan-Meier Survival Analysis
UVM	0.00023	Kaplan-Meier Survival Analysis