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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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Fusion gene:FBLN1-TCF7L2 (FusionGDB2 ID:HG2192TG6934)

Fusion Gene Summary for FBLN1-TCF7L2

check button Fusion gene summary
Fusion gene informationFusion gene name: FBLN1-TCF7L2
Fusion gene ID: hg2192tg6934
HgeneTgene
Gene symbol

FBLN1

TCF7L2

Gene ID

2192

6934

Gene namefibulin 1transcription factor 7 like 2
SynonymsFBLN|FIBL1TCF-4|TCF4
Cytomap('FBLN1')('TCF7L2')

22q13.31

10q25.2-q25.3

Type of geneprotein-codingprotein-coding
Descriptionfibulin-1transcription factor 7-like 2HMG box transcription factor 4T-cell factor 4T-cell-specific transcription factor 4hTCF-4transcription factor 7-like 2 (T-cell specific, HMG-box)
Modification date2020031320200315
UniProtAcc.

Q9NQB0

Ensembl transtripts involved in fusion geneENST00000476366, ENST00000262722, 
ENST00000327858, ENST00000340923, 
ENST00000348697, ENST00000402984, 
ENST00000442170, 
Fusion gene scores* DoF score15 X 14 X 8=168012 X 11 X 10=1320
# samples 1717
** MAII scorelog2(17/1680*10)=-3.30485458152842
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(17/1320*10)=-2.95693127810811
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FBLN1 [Title/Abstract] AND TCF7L2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFBLN1(45946495)-TCF7L2(114724314), # samples:1
Anticipated loss of major functional domain due to fusion event.FBLN1-TCF7L2 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
FBLN1-TCF7L2 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
FBLN1-TCF7L2 seems lost the major protein functional domain in Tgene partner, which is a transcription factor due to the frame-shifted ORF.
FBLN1-TCF7L2 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
HgeneFBLN1

GO:0001933

negative regulation of protein phosphorylation

11792823

HgeneFBLN1

GO:0007162

negative regulation of cell adhesion

11792823

HgeneFBLN1

GO:0007229

integrin-mediated signaling pathway

11792823

HgeneFBLN1

GO:0070373

negative regulation of ERK1 and ERK2 cascade

11792823

HgeneFBLN1

GO:0072378

blood coagulation, fibrin clot formation

7642629

HgeneFBLN1

GO:1900025

negative regulation of substrate adhesion-dependent cell spreading

11792823

HgeneFBLN1

GO:2000146

negative regulation of cell motility

11792823

HgeneFBLN1

GO:2000647

negative regulation of stem cell proliferation

11238726

TgeneTCF7L2

GO:0000122

negative regulation of transcription by RNA polymerase II

12799378

TgeneTCF7L2

GO:0006357

regulation of transcription by RNA polymerase II

9727977

TgeneTCF7L2

GO:0032092

positive regulation of protein binding

12799378

TgeneTCF7L2

GO:0032350

regulation of hormone metabolic process

15525634

TgeneTCF7L2

GO:0042593

glucose homeostasis

15525634

TgeneTCF7L2

GO:0043433

negative regulation of DNA-binding transcription factor activity

12799378

TgeneTCF7L2

GO:0045444

fat cell differentiation

10937998

TgeneTCF7L2

GO:0045892

negative regulation of transcription, DNA-templated

12799378|15525634

TgeneTCF7L2

GO:0045944

positive regulation of transcription by RNA polymerase II

9065401|19168596

TgeneTCF7L2

GO:0048625

myoblast fate commitment

10937998



check button Fusion gene information
* 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
ChimerDB4Non-Cancer149NFBLN1chr22

45946495

+TCF7L2chr10

114724314

+


Top

Fusion Gene ORF analysis for FBLN1-TCF7L2

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
3UTR-3CDSENST00000476366ENST00000355995FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-3CDSENST00000476366ENST00000534894FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-3CDSENST00000476366ENST00000536810FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-3CDSENST00000476366ENST00000543371FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-3CDSENST00000476366ENST00000545257FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-intronENST00000476366ENST00000349937FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-intronENST00000476366ENST00000352065FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-intronENST00000476366ENST00000355717FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-intronENST00000476366ENST00000369386FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-intronENST00000476366ENST00000369389FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-intronENST00000476366ENST00000369395FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-intronENST00000476366ENST00000369397FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-intronENST00000476366ENST00000466338FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-intronENST00000476366ENST00000538897FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
3UTR-intronENST00000476366ENST00000542695FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000262722ENST00000349937FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000262722ENST00000352065FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000262722ENST00000355717FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000262722ENST00000369386FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000262722ENST00000369389FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000262722ENST00000369395FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000262722ENST00000369397FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000262722ENST00000466338FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000262722ENST00000538897FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000262722ENST00000542695FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000327858ENST00000349937FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000327858ENST00000352065FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000327858ENST00000355717FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000327858ENST00000369386FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000327858ENST00000369389FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000327858ENST00000369395FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000327858ENST00000369397FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000327858ENST00000466338FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000327858ENST00000538897FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000327858ENST00000542695FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000340923ENST00000349937FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000340923ENST00000352065FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000340923ENST00000355717FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000340923ENST00000369386FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000340923ENST00000369389FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000340923ENST00000369395FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000340923ENST00000369397FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000340923ENST00000466338FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000340923ENST00000538897FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000340923ENST00000542695FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000348697ENST00000349937FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000348697ENST00000352065FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000348697ENST00000355717FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000348697ENST00000369386FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000348697ENST00000369389FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000348697ENST00000369395FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000348697ENST00000369397FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000348697ENST00000466338FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000348697ENST00000538897FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000348697ENST00000542695FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000402984ENST00000349937FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000402984ENST00000352065FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000402984ENST00000355717FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000402984ENST00000369386FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000402984ENST00000369389FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000402984ENST00000369395FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000402984ENST00000369397FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000402984ENST00000466338FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000402984ENST00000538897FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000402984ENST00000542695FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000442170ENST00000349937FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000442170ENST00000352065FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000442170ENST00000355717FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000442170ENST00000369386FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000442170ENST00000369389FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000442170ENST00000369395FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000442170ENST00000369397FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000442170ENST00000466338FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000442170ENST00000538897FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
5CDS-intronENST00000442170ENST00000542695FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000262722ENST00000355995FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000262722ENST00000534894FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000262722ENST00000536810FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000262722ENST00000543371FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000262722ENST00000545257FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000327858ENST00000355995FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000327858ENST00000534894FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000327858ENST00000536810FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000327858ENST00000543371FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000327858ENST00000545257FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000340923ENST00000355995FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000340923ENST00000534894FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000340923ENST00000536810FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000340923ENST00000543371FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000340923ENST00000545257FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000348697ENST00000355995FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000348697ENST00000534894FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000348697ENST00000536810FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000348697ENST00000543371FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000348697ENST00000545257FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000402984ENST00000355995FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000402984ENST00000534894FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000402984ENST00000536810FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000402984ENST00000543371FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000402984ENST00000545257FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000442170ENST00000355995FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000442170ENST00000534894FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000442170ENST00000536810FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000442170ENST00000543371FBLN1chr22

45946495

+TCF7L2chr10

114724314

+
Frame-shiftENST00000442170ENST00000545257FBLN1chr22

45946495

+TCF7L2chr10

114724314

+

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 FBLN1-TCF7L2


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)
FBLN1chr2245946495+TCF7L2chr10114724314+3.57E-060.9999964
FBLN1chr2245946495+TCF7L2chr10114724314+3.57E-060.9999964


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.
genomic feature of top 1%

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Fusion Protein Features for FBLN1-TCF7L2


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:45946495/:114724314)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.TCF7L2

Q9NQB0

FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Participates in the Wnt signaling pathway and modulates MYC expression by binding to its promoter in a sequence-specific manner. Acts as repressor in the absence of CTNNB1, and as activator in its presence. Activates transcription from promoters with several copies of the Tcf motif 5'-CCTTTGATC-3' in the presence of CTNNB1. TLE1, TLE2, TLE3 and TLE4 repress transactivation mediated by TCF7L2/TCF4 and CTNNB1. Expression of dominant-negative mutants results in cell-cycle arrest in G1. Necessary for the maintenance of the epithelial stem-cell compartment of the small intestine. {ECO:0000269|PubMed:12408868, ECO:0000269|PubMed:12727872, ECO:0000269|PubMed:19443654, ECO:0000269|PubMed:22699938, ECO:0000269|PubMed:9727977}.

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 FBLN1-TCF7L2


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 FBLN1-TCF7L2


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 FBLN1-TCF7L2


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 FBLN1-TCF7L2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFBLN1C1842422Synpolydactyly 23CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneFBLN1C0014175Endometriosis1CTD_human
HgeneFBLN1C0033578Prostatic Neoplasms1CTD_human
HgeneFBLN1C0269102Endometrioma1CTD_human
HgeneFBLN1C0376358Malignant neoplasm of prostate1CTD_human
TgeneC0036341Schizophrenia4PSYGENET
TgeneC0011860Diabetes Mellitus, Non-Insulin-Dependent3CTD_human
TgeneC0009402Colorectal Carcinoma2CTD_human;UNIPROT
TgeneC0009404Colorectal Neoplasms2CTD_human
TgeneC0001418Adenocarcinoma1CTD_human
TgeneC0005586Bipolar Disorder1PSYGENET
TgeneC0007102Malignant tumor of colon1CTD_human
TgeneC0007193Cardiomyopathy, Dilated1CTD_human
TgeneC0009375Colonic Neoplasms1CTD_human
TgeneC0010068Coronary heart disease1CTD_human
TgeneC0020507Hyperplasia1CTD_human
TgeneC0036337Schizoaffective Disorder1PSYGENET
TgeneC0087031Juvenile-Onset Still Disease1CTD_human
TgeneC0151744Myocardial Ischemia1CTD_human
TgeneC0205641Adenocarcinoma, Basal Cell1CTD_human
TgeneC0205642Adenocarcinoma, Oxyphilic1CTD_human
TgeneC0205643Carcinoma, Cribriform1CTD_human
TgeneC0205644Carcinoma, Granular Cell1CTD_human
TgeneC0205645Adenocarcinoma, Tubular1CTD_human
TgeneC0600519Ventricular Remodeling1CTD_human
TgeneC0600520Left Ventricle Remodeling1CTD_human
TgeneC1449563Cardiomyopathy, Familial Idiopathic1CTD_human
TgeneC1535926Neurodevelopmental Disorders1CTD_human
TgeneC2931456Prostate cancer, familial1CTD_human
TgeneC3495559Juvenile arthritis1CTD_human
TgeneC3714758Juvenile psoriatic arthritis1CTD_human
TgeneC4552091Polyarthritis, Juvenile, Rheumatoid Factor Negative1CTD_human
TgeneC4704862Polyarthritis, Juvenile, Rheumatoid Factor Positive1CTD_human
TgeneC4722327PROSTATE CANCER, HEREDITARY, 11CTD_human