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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:GSN-CTNNB1 (FusionGDB2 ID:HG2934TG1499)

Fusion Gene Summary for GSN-CTNNB1

check button Fusion gene summary
Fusion gene informationFusion gene name: GSN-CTNNB1
Fusion gene ID: hg2934tg1499
HgeneTgene
Gene symbol

GSN

CTNNB1

Gene ID

2934

1499

Gene namegelsolincatenin beta 1
SynonymsADF|AGELCTNNB|EVR7|MRD19|NEDSDV|armadillo
Cytomap('GSN')('CTNNB1')

9q33.2

3p22.1

Type of geneprotein-codingprotein-coding
Descriptiongelsolinactin-depolymerizing factorbrevinepididymis secretory sperm binding proteincatenin beta-1catenin (cadherin-associated protein), beta 1, 88kDa
Modification date2020032920200327
UniProtAcc

P06396

.
Ensembl transtripts involved in fusion geneENST00000341272, ENST00000373808, 
ENST00000373818, ENST00000373823, 
ENST00000394353, ENST00000412819, 
ENST00000436847, ENST00000449733, 
ENST00000373806, ENST00000373807, 
ENST00000485767, ENST00000545652, 
Fusion gene scores* DoF score21 X 16 X 8=268814 X 11 X 7=1078
# samples 2416
** MAII scorelog2(24/2688*10)=-3.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(16/1078*10)=-2.75221336786514
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GSN [Title/Abstract] AND CTNNB1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGSN(124095016)-CTNNB1(41240996), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneGSN

GO:0030041

actin filament polymerization

3020431

HgeneGSN

GO:0051014

actin filament severing

3020431

TgeneCTNNB1

GO:0000209

protein polyubiquitination

29374064

TgeneCTNNB1

GO:0008285

negative regulation of cell proliferation

12970740

TgeneCTNNB1

GO:0030997

regulation of centriole-centriole cohesion

18086858

TgeneCTNNB1

GO:0032355

response to estradiol

15304487

TgeneCTNNB1

GO:0033234

negative regulation of protein sumoylation

22155184

TgeneCTNNB1

GO:0043065

positive regulation of apoptotic process

12651860|12970740

TgeneCTNNB1

GO:0043161

proteasome-mediated ubiquitin-dependent protein catabolic process

29374064

TgeneCTNNB1

GO:0043525

positive regulation of neuron apoptotic process

19591802

TgeneCTNNB1

GO:0045893

positive regulation of transcription, DNA-templated

12970740|18787224

TgeneCTNNB1

GO:0045944

positive regulation of transcription by RNA polymerase II

9065402|11751639|12651860|14660579|18193033

TgeneCTNNB1

GO:0060070

canonical Wnt signaling pathway

10644691|12937339|19187541

TgeneCTNNB1

GO:0071681

cellular response to indole-3-methanol

10868478

TgeneCTNNB1

GO:0090279

regulation of calcium ion import

19996314

TgeneCTNNB1

GO:1904798

positive regulation of core promoter binding

22723415

TgeneCTNNB1

GO:2000008

regulation of protein localization to cell surface

19996314



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
ChimerDB4THCATCGA-EL-A3CN-01AGSNchr9

124095016

-CTNNB1chr3

41240996

+


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Fusion Gene ORF analysis for GSN-CTNNB1

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-5UTRENST00000341272ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000341272ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000341272ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000341272ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373808ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373808ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373808ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373808ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373818ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373818ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373818ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373818ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373823ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373823ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373823ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000373823ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000394353ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000394353ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000394353ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000394353ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000412819ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000412819ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000412819ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000412819ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000436847ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000436847ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000436847ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000436847ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000449733ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000449733ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000449733ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-5UTRENST00000449733ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000341272ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000341272ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000373808ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000373808ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000373818ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000373818ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000373823ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000373823ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000394353ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000394353ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000412819ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000412819ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000436847ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000436847ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000449733ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
3UTR-intronENST00000449733ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000373806ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000373806ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000373806ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000373806ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000373807ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000373807ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000373807ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000373807ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000485767ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000485767ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000485767ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000485767ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000545652ENST00000349496GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000545652ENST00000396183GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000545652ENST00000396185GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-5UTRENST00000545652ENST00000453024GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-intronENST00000373806ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-intronENST00000373806ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-intronENST00000373807ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-intronENST00000373807ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-intronENST00000485767ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-intronENST00000485767ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-intronENST00000545652ENST00000405570GSNchr9

124095016

-CTNNB1chr3

41240996

+
intron-intronENST00000545652ENST00000471014GSNchr9

124095016

-CTNNB1chr3

41240996

+

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 GSN-CTNNB1


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)


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Fusion Protein Features for GSN-CTNNB1


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/:124095016/:41240996)
- 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
GSN

P06396

.
FUNCTION: Calcium-regulated, actin-modulating protein that binds to the plus (or barbed) ends of actin monomers or filaments, preventing monomer exchange (end-blocking or capping). It can promote the assembly of monomers into filaments (nucleation) as well as sever filaments already formed. Plays a role in ciliogenesis. {ECO:0000269|PubMed:20393563}.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}.

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 GSN-CTNNB1


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 GSN-CTNNB1


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 GSN-CTNNB1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneGSNP06396DB01593ZincSmall moleculeApproved|Investigational
HgeneGSNP06396DB09130CopperSmall moleculeApproved|Investigational
HgeneGSNP06396DB14487Zinc acetateSmall moleculeApproved|Investigational

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Related Diseases for GSN-CTNNB1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGSNC1622345Meretoja syndrome6CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneGSNC0936273Familial Amyloid Polyneuropathy, Type IV3ORPHANET
HgeneGSNC0001787Osteoporosis, Age-Related1CTD_human
HgeneGSNC0002726Amyloidosis1GENOMICS_ENGLAND
HgeneGSNC0018800Cardiomegaly1CTD_human
HgeneGSNC0019193Hepatitis, Toxic1CTD_human
HgeneGSNC0023893Liver Cirrhosis, Experimental1CTD_human
HgeneGSNC0025500Mesothelioma1CTD_human
HgeneGSNC0029456Osteoporosis1CTD_human
HgeneGSNC0029459Osteoporosis, Senile1CTD_human
HgeneGSNC0030524Paratuberculosis1CTD_human
HgeneGSNC0036341Schizophrenia1PSYGENET
HgeneGSNC0043094Weight Gain1CTD_human
HgeneGSNC0268389Amyloidosis, familial visceral1GENOMICS_ENGLAND
HgeneGSNC0751406Post-Traumatic Osteoporosis1CTD_human
HgeneGSNC0860207Drug-Induced Liver Disease1CTD_human
HgeneGSNC0948089Acute Coronary Syndrome1CTD_human
HgeneGSNC1262760Hepatitis, Drug-Induced1CTD_human
HgeneGSNC1383860Cardiac Hypertrophy1CTD_human
HgeneGSNC3658290Drug-Induced Acute Liver Injury1CTD_human
HgeneGSNC4277682Chemical and Drug Induced Liver Injury1CTD_human
HgeneGSNC4279912Chemically-Induced Liver Toxicity1CTD_human
TgeneC0007102Malignant tumor of colon9CTD_human
TgeneC0009375Colonic Neoplasms9CTD_human
TgeneC3554449MENTAL RETARDATION, AUTOSOMAL DOMINANT 196CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneC0009402Colorectal Carcinoma5CTD_human;UNIPROT
TgeneC2239176Liver carcinoma5CGI;CTD_human;GENOMICS_ENGLAND;UNIPROT
TgeneC0009404Colorectal Neoplasms4CTD_human
TgeneC0001418Adenocarcinoma3CTD_human
TgeneC0019207Hepatoma, Morris3CTD_human
TgeneC0019208Hepatoma, Novikoff3CTD_human
TgeneC0023904Liver Neoplasms, Experimental3CTD_human
TgeneC0086404Experimental Hepatoma3CTD_human
TgeneC0205641Adenocarcinoma, Basal Cell3CTD_human
TgeneC0205642Adenocarcinoma, Oxyphilic3CTD_human
TgeneC0205643Carcinoma, Cribriform3CTD_human
TgeneC0205644Carcinoma, Granular Cell3CTD_human
TgeneC0205645Adenocarcinoma, Tubular3CTD_human
TgeneC0206711Pilomatrixoma3CTD_human;ORPHANET;UNIPROT
TgeneC1879526Aberrant Crypt Foci3CTD_human
TgeneC0001430Adenoma2CTD_human
TgeneC0006142Malignant neoplasm of breast2CTD_human
TgeneC0023903Liver neoplasms2CTD_human
TgeneC0025149Medulloblastoma2CGI;CTD_human;UNIPROT
TgeneC0027626Neoplasm Invasiveness2CTD_human
TgeneC0027708Nephroblastoma2CTD_human
TgeneC0033578Prostatic Neoplasms2CTD_human
TgeneC0036341Schizophrenia2PSYGENET
TgeneC0205646Adenoma, Basal Cell2CTD_human
TgeneC0205647Follicular adenoma2CTD_human
TgeneC0205648Adenoma, Microcystic2CTD_human
TgeneC0205649Adenoma, Monomorphic2CTD_human
TgeneC0205650Papillary adenoma2CTD_human
TgeneC0205651Adenoma, Trabecular2CTD_human
TgeneC0235874Disease Exacerbation2CTD_human
TgeneC0345904Malignant neoplasm of liver2CTD_human
TgeneC0376358Malignant neoplasm of prostate2CTD_human
TgeneC0678222Breast Carcinoma2CTD_human
TgeneC1140680Malignant neoplasm of ovary2CGI;CTD_human;UNIPROT
TgeneC1257931Mammary Neoplasms, Human2CTD_human
TgeneC1458155Mammary Neoplasms2CTD_human
TgeneC2930471Bilateral Wilms Tumor2CTD_human
TgeneC4539767EXUDATIVE VITREORETINOPATHY 72GENOMICS_ENGLAND;UNIPROT
TgeneC4704874Mammary Carcinoma, Human2CTD_human
TgeneC0000772Multiple congenital anomalies1CTD_human
TgeneC0001624Adrenal Gland Neoplasms1CTD_human
TgeneC0007193Cardiomyopathy, Dilated1CTD_human
TgeneC0007528Cecal Neoplasms1CTD_human
TgeneC0007621Neoplastic Cell Transformation1CTD_human
TgeneC0007873Uterine Cervical Neoplasm1CTD_human
TgeneC0010276Craniopharyngioma1CTD_human;ORPHANET
TgeneC0014518Toxic Epidermal Necrolysis1CTD_human
TgeneC0016059Fibrosis1CTD_human
TgeneC0018923Hemangiosarcoma1CTD_human
TgeneC0019193Hepatitis, Toxic1CTD_human
TgeneC0021841Intestinal Neoplasms1CTD_human
TgeneC0023890Liver Cirrhosis1CTD_human
TgeneC0024121Lung Neoplasms1CTD_human
TgeneC0026846Muscular Atrophy1CTD_human
TgeneC0027627Neoplasm Metastasis1CTD_human
TgeneC0027746Nerve Degeneration1CTD_human
TgeneC0030297Pancreatic Neoplasm1CTD_human
TgeneC0031149Peritoneal Neoplasms1CTD_human
TgeneC0038325Stevens-Johnson Syndrome1CTD_human
TgeneC0149721Left Ventricular Hypertrophy1CTD_human
TgeneC0151744Myocardial Ischemia1CTD_human
TgeneC0153437Malignant neoplasm of cecum1CTD_human
TgeneC0206624Hepatoblastoma1CGI;CTD_human
TgeneC0206669Hepatocellular Adenoma1CTD_human
TgeneC0206686Adrenocortical carcinoma1CTD_human
TgeneC0232347No-Reflow Phenomenon1CTD_human
TgeneC0239946Fibrosis, Liver1CTD_human
TgeneC0242379Malignant neoplasm of lung1CTD_human
TgeneC0242698Ventricular Dysfunction, Left1CTD_human
TgeneC0270948Neurogenic Muscular Atrophy1CTD_human
TgeneC0278875Adult Craniopharyngioma1CTD_human
TgeneC0279606Childhood Hepatocellular Carcinoma1ORPHANET
TgeneC0279607Adult Hepatocellular Carcinoma1ORPHANET
TgeneC0334634Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse1CTD_human
TgeneC0339539Familial Exudative Vitreoretinopathy1ORPHANET
TgeneC0342649Vascular calcification1CTD_human
TgeneC0345967Malignant mesothelioma1CTD_human
TgeneC0346627Intestinal Cancer1CTD_human
TgeneC0346647Malignant neoplasm of pancreas1CTD_human
TgeneC0346990Carcinomatosis of peritoneal cavity1CTD_human
TgeneC0376634Craniofacial Abnormalities1CTD_human
TgeneC0431128Papillary craniopharyngioma1CTD_human
TgeneC0431129Adamantinous Craniopharyngioma1CTD_human
TgeneC0431350Primary microcephaly1GENOMICS_ENGLAND
TgeneC0600519Ventricular Remodeling1CTD_human
TgeneC0600520Left Ventricle Remodeling1CTD_human
TgeneC0750887Adrenal Cancer1CTD_human
TgeneC0751061Craniopharyngioma, Child1CTD_human
TgeneC0751958Lymphoma, Lymphocytic, Intermediate1CTD_human
TgeneC0860207Drug-Induced Liver Disease1CTD_human
TgeneC0919267ovarian neoplasm1CGI;CTD_human
TgeneC1262760Hepatitis, Drug-Induced1CTD_human
TgeneC1274933Drug-Induced Stevens Johnson Syndrome1CTD_human
TgeneC1449563Cardiomyopathy, Familial Idiopathic1CTD_human
TgeneC1535926Neurodevelopmental Disorders1CTD_human
TgeneC1623038Cirrhosis1CTD_human
TgeneC1851402Exudative vitreoretinopathy 11ORPHANET
TgeneC2713615Slow-Flow Phenomenon1CTD_human
TgeneC3658290Drug-Induced Acute Liver Injury1CTD_human
TgeneC3658301Mycoplasma-Induced Stevens-Johnson Syndrome1CTD_human
TgeneC3658302Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum1CTD_human
TgeneC4048328cervical cancer1CTD_human
TgeneC4277682Chemical and Drug Induced Liver Injury1CTD_human
TgeneC4279912Chemically-Induced Liver Toxicity1CTD_human