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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:PTPRZ1-MET (FusionGDB2 ID:70147)

Fusion Gene Summary for PTPRZ1-MET

check button Fusion gene summary
Fusion gene informationFusion gene name: PTPRZ1-MET
Fusion gene ID: 70147
HgeneTgene
Gene symbol

PTPRZ1

MET

Gene ID

5803

8731

Gene nameprotein tyrosine phosphatase receptor type Z1RNA guanine-7 methyltransferase
SynonymsHPTPZ|HPTPzeta|PTP-ZETA|PTP18|PTPRZ|PTPZ|R-PTP-zeta-2|RPTPB|RPTPbeta|phosphacanCMT1|CMT1c|MET|Met|RG7MT1|cm1p|hCMT1|hMet
Cytomap

7q31.32

18p11.21

Type of geneprotein-codingprotein-coding
Descriptionreceptor-type tyrosine-protein phosphatase zetaprotein tyrosine phosphatase, receptor-type, Z polypeptide 1protein tyrosine phosphatase, receptor-type, zeta polypeptide 1protein-tyrosine phosphatase receptor type Z polypeptide 2receptor-type tyrosine mRNA cap guanine-N7 methyltransferaseRNA (guanine-7-) methyltransferasehcm1pmRNA (guanine-7-)methyltransferasemRNA (guanine-N(7)-)-methyltransferasemRNA cap methyltransferase
Modification date2020031320200329
UniProtAcc.

Q9H1A3

Ensembl transtripts involved in fusion geneENST00000393386, ENST00000449182, 
ENST00000483028, 		ENST00000397752, 
ENST00000318493, ENST00000436117, 
ENST00000495962, ENST00000539704, 
Fusion gene scores* DoF score15 X 14 X 7=147014 X 18 X 10=2520
# samples 1927
** MAII scorelog2(19/1470*10)=-2.95174483139278
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(27/2520*10)=-3.22239242133645
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PTPRZ1 [Title/Abstract] AND MET [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPTPRZ1(121513611)-MET(116339125), # samples:5
Anticipated loss of major functional domain due to fusion event.PTPRZ1-MET seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PTPRZ1-MET seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PTPRZ1-MET seems lost the major protein functional domain in Tgene partner, which is a kinase due to the frame-shifted ORF.
PTPRZ1-MET seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
PTPRZ1-MET seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
TgeneMET

GO:0006370

7-methylguanosine mRNA capping

27422871


check buttonFusion gene breakpoints across PTPRZ1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across MET (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4GBMTCGA-06-5417-01APTPRZ1chr7

121513611

+METchr7

116339125

+
ChimerDB4GBMTCGA-19-A6J5-01APTPRZ1chr7

121568275

+METchr7

116339125

+
ChimerDB4LGGTCGA-DU-7304-01APTPRZ1chr7

121513611

+METchr7

116339125

+
ChimerDB4LGGTCGA-DU-6407PTPRZ1chr7

121513611

+METchr7

116339124

+
ChimerDB4LGGTCGA-DU-6407PTPRZ1chr7

121513611

+METchr7

116371721

+
ChimerDB4GBMTCGA-06-5417-01APTPRZ1chr7

121513611

+METchr7

116339125

+
ChimerDB4GBMTCGA-06-5417-01APTPRZ1chr7

121513611

-METchr7

116339125

+
ChimerDB4LGGTCGA-DU-6407-02BPTPRZ1chr7

121513611

-METchr7

116339125

+
ChimerDB4LGGTCGA-DU-6407-02BPTPRZ1chr7

121513610

+METchr7

116335803

+
ChimerDB4LGGTCGA-DU-6407-02BPTPRZ1chr7

121513610

+METchr7

116339124

+


Top

Fusion Gene ORF analysis for PTPRZ1-MET

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5CDS-5UTRENST00000393386ENST00000397752PTPRZ1chr7

121513611

+METchr7

116339125

+
5CDS-5UTRENST00000393386ENST00000318493PTPRZ1chr7

121513611

+METchr7

116339125

+
5CDS-intronENST00000393386ENST00000436117PTPRZ1chr7

121513611

+METchr7

116339125

+
5CDS-intronENST00000393386ENST00000495962PTPRZ1chr7

121513611

+METchr7

116339125

+
5CDS-intronENST00000393386ENST00000539704PTPRZ1chr7

121513611

+METchr7

116339125

+
5CDS-5UTRENST00000449182ENST00000397752PTPRZ1chr7

121513611

+METchr7

116339125

+
5CDS-5UTRENST00000449182ENST00000318493PTPRZ1chr7

121513611

+METchr7

116339125

+
5CDS-intronENST00000449182ENST00000436117PTPRZ1chr7

121513611

+METchr7

116339125

+
5CDS-intronENST00000449182ENST00000495962PTPRZ1chr7

121513611

+METchr7

116339125

+
5CDS-intronENST00000449182ENST00000539704PTPRZ1chr7

121513611

+METchr7

116339125

+
intron-5UTRENST00000483028ENST00000397752PTPRZ1chr7

121513611

+METchr7

116339125

+
intron-5UTRENST00000483028ENST00000318493PTPRZ1chr7

121513611

+METchr7

116339125

+
intron-intronENST00000483028ENST00000436117PTPRZ1chr7

121513611

+METchr7

116339125

+
intron-intronENST00000483028ENST00000495962PTPRZ1chr7

121513611

+METchr7

116339125

+
intron-intronENST00000483028ENST00000539704PTPRZ1chr7

121513611

+METchr7

116339125

+
5CDS-5UTRENST00000393386ENST00000397752PTPRZ1chr7

121568275

+METchr7

116339125

+
5CDS-5UTRENST00000393386ENST00000318493PTPRZ1chr7

121568275

+METchr7

116339125

+
5CDS-intronENST00000393386ENST00000436117PTPRZ1chr7

121568275

+METchr7

116339125

+
5CDS-intronENST00000393386ENST00000495962PTPRZ1chr7

121568275

+METchr7

116339125

+
5CDS-intronENST00000393386ENST00000539704PTPRZ1chr7

121568275

+METchr7

116339125

+
5CDS-5UTRENST00000449182ENST00000397752PTPRZ1chr7

121568275

+METchr7

116339125

+
5CDS-5UTRENST00000449182ENST00000318493PTPRZ1chr7

121568275

+METchr7

116339125

+
5CDS-intronENST00000449182ENST00000436117PTPRZ1chr7

121568275

+METchr7

116339125

+
5CDS-intronENST00000449182ENST00000495962PTPRZ1chr7

121568275

+METchr7

116339125

+
5CDS-intronENST00000449182ENST00000539704PTPRZ1chr7

121568275

+METchr7

116339125

+
intron-5UTRENST00000483028ENST00000397752PTPRZ1chr7

121568275

+METchr7

116339125

+
intron-5UTRENST00000483028ENST00000318493PTPRZ1chr7

121568275

+METchr7

116339125

+
intron-intronENST00000483028ENST00000436117PTPRZ1chr7

121568275

+METchr7

116339125

+
intron-intronENST00000483028ENST00000495962PTPRZ1chr7

121568275

+METchr7

116339125

+
intron-intronENST00000483028ENST00000539704PTPRZ1chr7

121568275

+METchr7

116339125

+
5CDS-5UTRENST00000393386ENST00000397752PTPRZ1chr7

121513611

+METchr7

116339124

+
5CDS-5UTRENST00000393386ENST00000318493PTPRZ1chr7

121513611

+METchr7

116339124

+
5CDS-intronENST00000393386ENST00000436117PTPRZ1chr7

121513611

+METchr7

116339124

+
5CDS-intronENST00000393386ENST00000495962PTPRZ1chr7

121513611

+METchr7

116339124

+
5CDS-intronENST00000393386ENST00000539704PTPRZ1chr7

121513611

+METchr7

116339124

+
5CDS-5UTRENST00000449182ENST00000397752PTPRZ1chr7

121513611

+METchr7

116339124

+
5CDS-5UTRENST00000449182ENST00000318493PTPRZ1chr7

121513611

+METchr7

116339124

+
5CDS-intronENST00000449182ENST00000436117PTPRZ1chr7

121513611

+METchr7

116339124

+
5CDS-intronENST00000449182ENST00000495962PTPRZ1chr7

121513611

+METchr7

116339124

+
5CDS-intronENST00000449182ENST00000539704PTPRZ1chr7

121513611

+METchr7

116339124

+
intron-5UTRENST00000483028ENST00000397752PTPRZ1chr7

121513611

+METchr7

116339124

+
intron-5UTRENST00000483028ENST00000318493PTPRZ1chr7

121513611

+METchr7

116339124

+
intron-intronENST00000483028ENST00000436117PTPRZ1chr7

121513611

+METchr7

116339124

+
intron-intronENST00000483028ENST00000495962PTPRZ1chr7

121513611

+METchr7

116339124

+
intron-intronENST00000483028ENST00000539704PTPRZ1chr7

121513611

+METchr7

116339124

+
Frame-shiftENST00000393386ENST00000397752PTPRZ1chr7

121513611

+METchr7

116371721

+
Frame-shiftENST00000393386ENST00000318493PTPRZ1chr7

121513611

+METchr7

116371721

+
Frame-shiftENST00000393386ENST00000436117PTPRZ1chr7

121513611

+METchr7

116371721

+
5CDS-3UTRENST00000393386ENST00000495962PTPRZ1chr7

121513611

+METchr7

116371721

+
5CDS-intronENST00000393386ENST00000539704PTPRZ1chr7

121513611

+METchr7

116371721

+
Frame-shiftENST00000449182ENST00000397752PTPRZ1chr7

121513611

+METchr7

116371721

+
Frame-shiftENST00000449182ENST00000318493PTPRZ1chr7

121513611

+METchr7

116371721

+
Frame-shiftENST00000449182ENST00000436117PTPRZ1chr7

121513611

+METchr7

116371721

+
5CDS-3UTRENST00000449182ENST00000495962PTPRZ1chr7

121513611

+METchr7

116371721

+
5CDS-intronENST00000449182ENST00000539704PTPRZ1chr7

121513611

+METchr7

116371721

+
intron-3CDSENST00000483028ENST00000397752PTPRZ1chr7

121513611

+METchr7

116371721

+
intron-3CDSENST00000483028ENST00000318493PTPRZ1chr7

121513611

+METchr7

116371721

+
intron-3CDSENST00000483028ENST00000436117PTPRZ1chr7

121513611

+METchr7

116371721

+
intron-3UTRENST00000483028ENST00000495962PTPRZ1chr7

121513611

+METchr7

116371721

+
intron-intronENST00000483028ENST00000539704PTPRZ1chr7

121513611

+METchr7

116371721

+
5CDS-intronENST00000393386ENST00000397752PTPRZ1chr7

121513610

+METchr7

116335803

+
5CDS-intronENST00000393386ENST00000318493PTPRZ1chr7

121513610

+METchr7

116335803

+
5CDS-intronENST00000393386ENST00000436117PTPRZ1chr7

121513610

+METchr7

116335803

+
5CDS-intronENST00000393386ENST00000495962PTPRZ1chr7

121513610

+METchr7

116335803

+
5CDS-intronENST00000393386ENST00000539704PTPRZ1chr7

121513610

+METchr7

116335803

+
5CDS-intronENST00000449182ENST00000397752PTPRZ1chr7

121513610

+METchr7

116335803

+
5CDS-intronENST00000449182ENST00000318493PTPRZ1chr7

121513610

+METchr7

116335803

+
5CDS-intronENST00000449182ENST00000436117PTPRZ1chr7

121513610

+METchr7

116335803

+
5CDS-intronENST00000449182ENST00000495962PTPRZ1chr7

121513610

+METchr7

116335803

+
5CDS-intronENST00000449182ENST00000539704PTPRZ1chr7

121513610

+METchr7

116335803

+
intron-intronENST00000483028ENST00000397752PTPRZ1chr7

121513610

+METchr7

116335803

+
intron-intronENST00000483028ENST00000318493PTPRZ1chr7

121513610

+METchr7

116335803

+
intron-intronENST00000483028ENST00000436117PTPRZ1chr7

121513610

+METchr7

116335803

+
intron-intronENST00000483028ENST00000495962PTPRZ1chr7

121513610

+METchr7

116335803

+
intron-intronENST00000483028ENST00000539704PTPRZ1chr7

121513610

+METchr7

116335803

+
5CDS-5UTRENST00000393386ENST00000397752PTPRZ1chr7

121513610

+METchr7

116339124

+
5CDS-5UTRENST00000393386ENST00000318493PTPRZ1chr7

121513610

+METchr7

116339124

+
5CDS-intronENST00000393386ENST00000436117PTPRZ1chr7

121513610

+METchr7

116339124

+
5CDS-intronENST00000393386ENST00000495962PTPRZ1chr7

121513610

+METchr7

116339124

+
5CDS-intronENST00000393386ENST00000539704PTPRZ1chr7

121513610

+METchr7

116339124

+
5CDS-5UTRENST00000449182ENST00000397752PTPRZ1chr7

121513610

+METchr7

116339124

+
5CDS-5UTRENST00000449182ENST00000318493PTPRZ1chr7

121513610

+METchr7

116339124

+
5CDS-intronENST00000449182ENST00000436117PTPRZ1chr7

121513610

+METchr7

116339124

+
5CDS-intronENST00000449182ENST00000495962PTPRZ1chr7

121513610

+METchr7

116339124

+
5CDS-intronENST00000449182ENST00000539704PTPRZ1chr7

121513610

+METchr7

116339124

+
intron-5UTRENST00000483028ENST00000397752PTPRZ1chr7

121513610

+METchr7

116339124

+
intron-5UTRENST00000483028ENST00000318493PTPRZ1chr7

121513610

+METchr7

116339124

+
intron-intronENST00000483028ENST00000436117PTPRZ1chr7

121513610

+METchr7

116339124

+
intron-intronENST00000483028ENST00000495962PTPRZ1chr7

121513610

+METchr7

116339124

+
intron-intronENST00000483028ENST00000539704PTPRZ1chr7

121513610

+METchr7

116339124

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)		BP loci
(transcript)		Predicted start
(transcript)		Predicted stop
(transcript)		Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for PTPRZ1-MET


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
PTPRZ1chr7121513611+METchr7116371721+0.23213910.76786095
PTPRZ1chr7121513611+METchr7116339124+0.0053062430.9946938
PTPRZ1chr7121513611+METchr7116339124+0.0053062430.9946938
PTPRZ1chr7121513611+METchr7116339124+0.0053062430.9946938
PTPRZ1chr7121568275+METchr7116339124+7.76E-060.99999225
PTPRZ1chr7121513611+METchr7116371721+0.23213910.76786095
PTPRZ1chr7121513611+METchr7116339124+0.0053062430.9946938
PTPRZ1chr7121513611+METchr7116339124+0.0053062430.9946938
PTPRZ1chr7121513611+METchr7116339124+0.0053062430.9946938
PTPRZ1chr7121568275+METchr7116339124+7.76E-060.99999225

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for PTPRZ1-MET


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.MET

Q9H1A3

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for PTPRZ1-MET


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for PTPRZ1-MET


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for PTPRZ1-MET


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for PTPRZ1-MET


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePTPRZ1C0036341Schizophrenia3PSYGENET
HgenePTPRZ1C0004681Bagassosis1CTD_human
HgenePTPRZ1C0032273Pneumoconiosis1CTD_human
HgenePTPRZ1C0079487Helicobacter Infections1CTD_human
HgenePTPRZ1C1838332HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO1GENOMICS_ENGLAND
TgeneMETC1306837Papillary Renal Cell Carcinoma9CGI;CLINGEN;CTD_human;ORPHANET
TgeneMETC1336078Papillary renal cell carcinoma, sporadic7CLINGEN
TgeneMETC1336839Type 1 Papillary Renal Cell Carcinoma5UNIPROT
TgeneMETC0007131Non-Small Cell Lung Carcinoma4CGI;CTD_human
TgeneMETC1836723Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum4ORPHANET
TgeneMETC4085248OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO4ORPHANET
TgeneMETC0001418Adenocarcinoma2CTD_human
TgeneMETC0004352Autistic Disorder2CTD_human
TgeneMETC0024623Malignant neoplasm of stomach2CGI;CTD_human;UNIPROT
TgeneMETC0027627Neoplasm Metastasis2CTD_human
TgeneMETC0038356Stomach Neoplasms2CGI;CTD_human
TgeneMETC0205641Adenocarcinoma, Basal Cell2CTD_human
TgeneMETC0205642Adenocarcinoma, Oxyphilic2CTD_human
TgeneMETC0205643Carcinoma, Cribriform2CTD_human
TgeneMETC0205644Carcinoma, Granular Cell2CTD_human
TgeneMETC0205645Adenocarcinoma, Tubular2CTD_human
TgeneMETC1708349Hereditary Diffuse Gastric Cancer2CTD_human
TgeneMETC0004114Astrocytoma1CTD_human
TgeneMETC0007097Carcinoma1CTD_human
TgeneMETC0007134Renal Cell Carcinoma1CTD_human
TgeneMETC0007137Squamous cell carcinoma1CTD_human
TgeneMETC0009241Cognition Disorders1CTD_human
TgeneMETC0014859Esophageal Neoplasms1CTD_human
TgeneMETC0017636Glioblastoma1CTD_human
TgeneMETC0019189Hepatitis, Chronic1CTD_human
TgeneMETC0019207Hepatoma, Morris1CTD_human
TgeneMETC0019208Hepatoma, Novikoff1CTD_human
TgeneMETC0023467Leukemia, Myelocytic, Acute1CTD_human
TgeneMETC0023904Liver Neoplasms, Experimental1CTD_human
TgeneMETC0024121Lung Neoplasms1CTD_human
TgeneMETC0024232Lymphatic Metastasis1CTD_human
TgeneMETC0025202melanoma1CTD_human
TgeneMETC0026998Acute Myeloid Leukemia, M11CTD_human
TgeneMETC0027626Neoplasm Invasiveness1CTD_human
TgeneMETC0027819Neuroblastoma1CTD_human
TgeneMETC0029463Osteosarcoma1CTD_human
TgeneMETC0033578Prostatic Neoplasms1CTD_human
TgeneMETC0036341Schizophrenia1CTD_human
TgeneMETC0037199Sinusitis1CTD_human
TgeneMETC0086404Experimental Hepatoma1CTD_human
TgeneMETC0149519Chronic Persistent Hepatitis1CTD_human
TgeneMETC0205696Anaplastic carcinoma1CTD_human
TgeneMETC0205697Carcinoma, Spindle-Cell1CTD_human
TgeneMETC0205698Undifferentiated carcinoma1CTD_human
TgeneMETC0205699Carcinomatosis1CTD_human
TgeneMETC0205768Subependymal Giant Cell Astrocytoma1CTD_human
TgeneMETC0242379Malignant neoplasm of lung1CTD_human
TgeneMETC0279606Childhood Hepatocellular Carcinoma1ORPHANET
TgeneMETC0279702Conventional (Clear Cell) Renal Cell Carcinoma1CGI;CTD_human
TgeneMETC0280783Juvenile Pilocytic Astrocytoma1CTD_human
TgeneMETC0280785Diffuse Astrocytoma1CTD_human
TgeneMETC0334579Anaplastic astrocytoma1CTD_human
TgeneMETC0334580Protoplasmic astrocytoma1CTD_human
TgeneMETC0334581Gemistocytic astrocytoma1CTD_human
TgeneMETC0334582Fibrillary Astrocytoma1CTD_human
TgeneMETC0334583Pilocytic Astrocytoma1CTD_human
TgeneMETC0334588Giant Cell Glioblastoma1CTD_human
TgeneMETC0338070Childhood Cerebral Astrocytoma1CTD_human
TgeneMETC0345967Malignant mesothelioma1CTD_human
TgeneMETC0376358Malignant neoplasm of prostate1CTD_human
TgeneMETC0520463Chronic active hepatitis1CTD_human
TgeneMETC0524611Cryptogenic Chronic Hepatitis1CTD_human
TgeneMETC0546837Malignant neoplasm of esophagus1CTD_human
TgeneMETC0547065Mixed oligoastrocytoma1CTD_human
TgeneMETC0750935Cerebral Astrocytoma1CTD_human
TgeneMETC0750936Intracranial Astrocytoma1CTD_human
TgeneMETC0919267ovarian neoplasm1CTD_human
TgeneMETC1140680Malignant neoplasm of ovary1CTD_human
TgeneMETC1266042Chromophobe Renal Cell Carcinoma1CTD_human
TgeneMETC1266043Sarcomatoid Renal Cell Carcinoma1CTD_human
TgeneMETC1266044Collecting Duct Carcinoma of the Kidney1CTD_human
TgeneMETC1621958Glioblastoma Multiforme1CTD_human
TgeneMETC1704230Grade I Astrocytoma1CTD_human
TgeneMETC1708353Hereditary Paraganglioma-Pheochromocytoma Syndrome1CLINGEN
TgeneMETC1876165Copper-Overload Cirrhosis1CTD_human
TgeneMETC1879321Acute Myeloid Leukemia (AML-M2)1CTD_human
TgeneMETC2239176Liver carcinoma1CGI;CTD_human;UNIPROT
TgeneMETC3711374Nonsyndromic Deafness1CLINGEN
TgeneMETC4084709DEAFNESS, AUTOSOMAL RECESSIVE 971CTD_human;UNIPROT