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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:PLXNC1-TXNRD1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PLXNC1-TXNRD1
FusionPDB ID: 66588
FusionGDB2.0 ID: 66588
HgeneTgene
Gene symbol

PLXNC1

TXNRD1

Gene ID

10154

7296

Gene nameplexin C1thioredoxin reductase 1
SynonymsCD232|PLXN-C1|VESPRGRIM-12|TR|TR1|TRXR1|TXNR
Cytomap

12q22

12q23.3

Type of geneprotein-codingprotein-coding
Descriptionplexin-C1plexin (semaphorin receptor)receptor for viral semaphorin proteinreceptor for virally-encoded semaphorinvirus-encoded semaphorin protein receptorthioredoxin reductase 1, cytoplasmicKM-102-derived reductase-like factorgene associated with retinoic and IFN-induced mortality 12 proteingene associated with retinoic and interferon-induced mortality 12 proteinoxidoreductasetestis tissue sperm-bindi
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000258526, ENST00000545312, 
ENST00000547057, ENST00000551495, 
ENST00000378070, ENST00000397736, 
ENST00000427956, ENST00000526950, 
ENST00000526006, ENST00000354940, 
ENST00000388854, ENST00000429002, 
ENST00000503506, ENST00000524698, 
ENST00000525566, ENST00000526390, 
ENST00000526691, ENST00000529546, 
ENST00000542918, ENST00000540716, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 6 X 5=21011 X 11 X 4=484
# samples 1012
** MAII scorelog2(10/210*10)=-1.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/484*10)=-2.01197264166608
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: PLXNC1 [Title/Abstract] AND TXNRD1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PLXNC1(94676177)-TXNRD1(104742131), # samples:3
Anticipated loss of major functional domain due to fusion event.PLXNC1-TXNRD1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
PLXNC1-TXNRD1 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
PLXNC1-TXNRD1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
PLXNC1-TXNRD1 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
PLXNC1-TXNRD1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PLXNC1-TXNRD1 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
PLXNC1-TXNRD1 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene 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

check buttonFusion gene breakpoints across PLXNC1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across TXNRD1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4SARCTCGA-DX-A3U5-01APLXNC1chr12

94676177

-TXNRD1chr12

104742131

+
ChimerDB4SARCTCGA-DX-A3U5-01APLXNC1chr12

94676177

+TXNRD1chr12

104742131

+
ChimerDB4SARCTCGA-DX-A3U5PLXNC1chr12

94676177

+TXNRD1chr12

104742130

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000258526PLXNC1chr1294676177+ENST00000540716TXNRD1chr12104742131+464441283341901385
ENST00000547057PLXNC1chr1294676177+ENST00000540716TXNRD1chr12104742131+177312571411319392
ENST00000545312PLXNC1chr1294676177+ENST00000540716TXNRD1chr12104742131+1188672267734155
ENST00000258526PLXNC1chr1294676177+ENST00000540716TXNRD1chr12104742130+464441283341901385
ENST00000547057PLXNC1chr1294676177+ENST00000540716TXNRD1chr12104742130+177312571411319392
ENST00000545312PLXNC1chr1294676177+ENST00000540716TXNRD1chr12104742130+1188672267734155

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
ENST00000258526ENST00000540716PLXNC1chr1294676177+TXNRD1chr12104742131+0.0005143550.9994856
ENST00000547057ENST00000540716PLXNC1chr1294676177+TXNRD1chr12104742131+0.0007276950.9992723
ENST00000545312ENST00000540716PLXNC1chr1294676177+TXNRD1chr12104742131+0.256721880.7432781
ENST00000258526ENST00000540716PLXNC1chr1294676177+TXNRD1chr12104742130+0.0005143550.9994856
ENST00000547057ENST00000540716PLXNC1chr1294676177+TXNRD1chr12104742130+0.0007276950.9992723
ENST00000545312ENST00000540716PLXNC1chr1294676177+TXNRD1chr12104742130+0.256721880.7432781

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>66588_66588_1_PLXNC1-TXNRD1_PLXNC1_chr12_94676177_ENST00000258526_TXNRD1_chr12_104742130_ENST00000540716_length(amino acids)=1385AA_BP=1365
MLPPPPLHRLPERACRAPPSPLSFLGELRGWGGRGSPSARRNRRRRRPRLRCRAPEPPSPPRALPGGGPPSPMEVSRRKAPPRPPRPAAP
LPLLAYLLALAAPGRGADEPVWRSEQAIGAIAASQEDGVFVASGSCLDQLDYSLEHSLSRLYRDQAGNCTEPVSLAPPARPRPGSSFSKL
LLPYREGAAGLGGLLLTGWTFDRGACEVRPLGNLSRNSLRNGTEVVSCHPQGSTAGVVYRAGRNNRWYLAVAATYVLPEPETASRCNPAA
SDHDTAIALKDTEGRSLATQELGRLKLCEGAGSLHFVDAFLWNGSIYFPYYPYNYTSGAATGWPSMARIAQSTEVLFQGQASLDCGHGHP
DGRRLLLSSSLVEALDVWAGVFSAAAGEGQERRSPTTTALCLFRMSEIQARAKRVSWDFKTAESHCKEGDQPERVQPIASSTLIHSDLTS
VYGTVVMNRTVLFLGTGDGQLLKVILGENLTSNCPEVIYEIKEETPVFYKLVPDPVKNIYIYLTAGKEVRRIRVANCNKHKSCSECLTAT
DPHCGWCHSLQRCTFQGDCVHSENLENWLDISSGAKKCPKIQIIRSSKEKTTVTMVGSFSPRHSKCMVKNVDSSRELCQNKSQPNRTCTC
SIPTRATYKDVSVVNVMFSFGSWNLSDRFNFTNCSSLKECPACVETGCAWCKSARRCIHPFTACDPSDYERNQEQCPVAVEKTSGGGRPK
ENKGNRTNQALQVFYIKSIEPQKVSTLGKSNVIVTGANFTRASNITMILKGTSTCDKDVIQVSHVLNDTHMKFSLPSSRKEMKDVCIQFD
GGNCSSVGSLSYIALPHCSLIFPATTWISGGQNITMMGRNFDVIDNLIISHELKGNINVSEYCVATYCGFLAPSLKSSKVRTNVTVKLRV
QDTYLDCGTLQYREDPRFTGYRVESEVDTELEVKIQKENDNFNISKKDIEITLFHGENGQLNCSFENITRNQDLTTILCKIKGIKTASTI
ANSSKKVRVKLGNLELYVEQESVPSTWYFLIVLPVLLVIVIFAAVGVTRHKSKELSRKQSQQLELLESELRKEIRDGFAELQMDKLDVVD
SFGTVPFLDYKHFALRTFFPESGGFTHIFTEDMHNRDANDKNESLTALDALICNKSFLVTVIHTLEKQKNFSVKDRCLFASFLTIALQTK
LVYLTSILEVLTRDLMEQCSNMQPKLMLRRTESVVEKLLTNWMSVCLSGFLRETVGEPFYLLVTTLNQKINKGPVDVITCKALYTLNEDW
LLWQVPEFSTVALNVVFEKIPENESADVCRNISVNVLDCDTIGQAKEKIFQAFLSKNGSPYGLQLNEIGLELQMGTRQKELLDIDSSSVI

--------------------------------------------------------------

>66588_66588_2_PLXNC1-TXNRD1_PLXNC1_chr12_94676177_ENST00000258526_TXNRD1_chr12_104742131_ENST00000540716_length(amino acids)=1385AA_BP=1365
MLPPPPLHRLPERACRAPPSPLSFLGELRGWGGRGSPSARRNRRRRRPRLRCRAPEPPSPPRALPGGGPPSPMEVSRRKAPPRPPRPAAP
LPLLAYLLALAAPGRGADEPVWRSEQAIGAIAASQEDGVFVASGSCLDQLDYSLEHSLSRLYRDQAGNCTEPVSLAPPARPRPGSSFSKL
LLPYREGAAGLGGLLLTGWTFDRGACEVRPLGNLSRNSLRNGTEVVSCHPQGSTAGVVYRAGRNNRWYLAVAATYVLPEPETASRCNPAA
SDHDTAIALKDTEGRSLATQELGRLKLCEGAGSLHFVDAFLWNGSIYFPYYPYNYTSGAATGWPSMARIAQSTEVLFQGQASLDCGHGHP
DGRRLLLSSSLVEALDVWAGVFSAAAGEGQERRSPTTTALCLFRMSEIQARAKRVSWDFKTAESHCKEGDQPERVQPIASSTLIHSDLTS
VYGTVVMNRTVLFLGTGDGQLLKVILGENLTSNCPEVIYEIKEETPVFYKLVPDPVKNIYIYLTAGKEVRRIRVANCNKHKSCSECLTAT
DPHCGWCHSLQRCTFQGDCVHSENLENWLDISSGAKKCPKIQIIRSSKEKTTVTMVGSFSPRHSKCMVKNVDSSRELCQNKSQPNRTCTC
SIPTRATYKDVSVVNVMFSFGSWNLSDRFNFTNCSSLKECPACVETGCAWCKSARRCIHPFTACDPSDYERNQEQCPVAVEKTSGGGRPK
ENKGNRTNQALQVFYIKSIEPQKVSTLGKSNVIVTGANFTRASNITMILKGTSTCDKDVIQVSHVLNDTHMKFSLPSSRKEMKDVCIQFD
GGNCSSVGSLSYIALPHCSLIFPATTWISGGQNITMMGRNFDVIDNLIISHELKGNINVSEYCVATYCGFLAPSLKSSKVRTNVTVKLRV
QDTYLDCGTLQYREDPRFTGYRVESEVDTELEVKIQKENDNFNISKKDIEITLFHGENGQLNCSFENITRNQDLTTILCKIKGIKTASTI
ANSSKKVRVKLGNLELYVEQESVPSTWYFLIVLPVLLVIVIFAAVGVTRHKSKELSRKQSQQLELLESELRKEIRDGFAELQMDKLDVVD
SFGTVPFLDYKHFALRTFFPESGGFTHIFTEDMHNRDANDKNESLTALDALICNKSFLVTVIHTLEKQKNFSVKDRCLFASFLTIALQTK
LVYLTSILEVLTRDLMEQCSNMQPKLMLRRTESVVEKLLTNWMSVCLSGFLRETVGEPFYLLVTTLNQKINKGPVDVITCKALYTLNEDW
LLWQVPEFSTVALNVVFEKIPENESADVCRNISVNVLDCDTIGQAKEKIFQAFLSKNGSPYGLQLNEIGLELQMGTRQKELLDIDSSSVI

--------------------------------------------------------------

>66588_66588_3_PLXNC1-TXNRD1_PLXNC1_chr12_94676177_ENST00000545312_TXNRD1_chr12_104742130_ENST00000540716_length(amino acids)=155AA_BP=135
MLVTTLNQKINKGPVDVITCKALYTLNEDWLLWQVPEFSTVALNVVFEKIPENESADVCRNISVNVLDCDTIGQAKEKIFQAFLSKNGSP

--------------------------------------------------------------

>66588_66588_4_PLXNC1-TXNRD1_PLXNC1_chr12_94676177_ENST00000545312_TXNRD1_chr12_104742131_ENST00000540716_length(amino acids)=155AA_BP=135
MLVTTLNQKINKGPVDVITCKALYTLNEDWLLWQVPEFSTVALNVVFEKIPENESADVCRNISVNVLDCDTIGQAKEKIFQAFLSKNGSP

--------------------------------------------------------------

>66588_66588_5_PLXNC1-TXNRD1_PLXNC1_chr12_94676177_ENST00000547057_TXNRD1_chr12_104742130_ENST00000540716_length(amino acids)=392AA_BP=372
MSLSVLFLFLFLRTVKIAICFHFWFLSYHVPLMQHLCLLAAVGVTRHKSKELSRKQSQQLELLESELRKEIRDGFAELQMDKLDVVDSFG
TVPFLDYKHFALRTFFPESGGFTHIFTEDMHNRDANDKNESLTALDALICNKSFLVTVIHTLEKQKNFSVKDRCLFASFLTIALQTKLVY
LTSILEVLTRDLMEQCSNMQPKLMLRRTESVVEKLLTNWMSVCLSGFLRETVGEPFYLLVTTLNQKINKGPVDVITCKALYTLNEDWLLW
QVPEFSTVALNVVFEKIPENESADVCRNISVNVLDCDTIGQAKEKIFQAFLSKNGSPYGLQLNEIGLELQMGTRQKELLDIDSSSVILED

--------------------------------------------------------------

>66588_66588_6_PLXNC1-TXNRD1_PLXNC1_chr12_94676177_ENST00000547057_TXNRD1_chr12_104742131_ENST00000540716_length(amino acids)=392AA_BP=372
MSLSVLFLFLFLRTVKIAICFHFWFLSYHVPLMQHLCLLAAVGVTRHKSKELSRKQSQQLELLESELRKEIRDGFAELQMDKLDVVDSFG
TVPFLDYKHFALRTFFPESGGFTHIFTEDMHNRDANDKNESLTALDALICNKSFLVTVIHTLEKQKNFSVKDRCLFASFLTIALQTKLVY
LTSILEVLTRDLMEQCSNMQPKLMLRRTESVVEKLLTNWMSVCLSGFLRETVGEPFYLLVTTLNQKINKGPVDVITCKALYTLNEDWLLW
QVPEFSTVALNVVFEKIPENESADVCRNISVNVLDCDTIGQAKEKIFQAFLSKNGSPYGLQLNEIGLELQMGTRQKELLDIDSSSVILED

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr12:94676177/chr12:104742131)
- 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
..
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.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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgenePLXNC1chr12:94676177chr12:104742130ENST00000258526+233135_4521293.01569.0DomainSema
HgenePLXNC1chr12:94676177chr12:104742131ENST00000258526+233135_4521293.01569.0DomainSema
HgenePLXNC1chr12:94676177chr12:104742130ENST00000258526+233135_9441293.01569.0Topological domainExtracellular
HgenePLXNC1chr12:94676177chr12:104742131ENST00000258526+233135_9441293.01569.0Topological domainExtracellular
HgenePLXNC1chr12:94676177chr12:104742130ENST00000258526+2331945_9651293.01569.0TransmembraneHelical
HgenePLXNC1chr12:94676177chr12:104742131ENST00000258526+2331945_9651293.01569.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgenePLXNC1chr12:94676177chr12:104742130ENST00000258526+2331966_15681293.01569.0Topological domainCytoplasmic
HgenePLXNC1chr12:94676177chr12:104742131ENST00000258526+2331966_15681293.01569.0Topological domainCytoplasmic
TgeneTXNRD1chr12:94676177chr12:104742130ENST00000388854131556_156529.0550.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742130ENST00000503506131556_156477.0500.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742130ENST00000524698131556_156477.0500.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742130ENST00000525566151756_156627.0650.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742130ENST00000526390151756_156521.0544.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742130ENST00000526691131556_156529.0552.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742131ENST00000388854131556_156529.0550.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742131ENST00000503506131556_156477.0500.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742131ENST00000524698131556_156477.0500.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742131ENST00000525566151756_156627.0650.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742131ENST00000526390151756_156521.0544.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742131ENST00000526691131556_156529.0552.0DomainGlutaredoxin
TgeneTXNRD1chr12:94676177chr12:104742130ENST000003888541315192_209529.0550.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742130ENST000005035061315192_209477.0500.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742130ENST000005246981315192_209477.0500.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742130ENST000005255661517192_209627.0650.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742130ENST000005263901517192_209521.0544.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742130ENST000005266911315192_209529.0552.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742131ENST000003888541315192_209529.0550.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742131ENST000005035061315192_209477.0500.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742131ENST000005246981315192_209477.0500.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742131ENST000005255661517192_209627.0650.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742131ENST000005263901517192_209521.0544.0Nucleotide bindingFAD
TgeneTXNRD1chr12:94676177chr12:104742131ENST000005266911315192_209529.0552.0Nucleotide bindingFAD


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
PLXNC1
TXNRD1


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to PLXNC1-TXNRD1


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to PLXNC1-TXNRD1


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource