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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:AGRN-BAD (FusionGDB2 ID:HG375790TG572)

Fusion Gene Summary for AGRN-BAD

check button Fusion gene summary
Fusion gene informationFusion gene name: AGRN-BAD
Fusion gene ID: hg375790tg572
HgeneTgene
Gene symbol

AGRN

BAD

Gene ID

375790

572

Gene nameagrinBCL2 associated agonist of cell death
SynonymsAGRIN|CMS8|CMSPPDBBC2|BCL2L8
Cytomap('AGRN')('BAD')

1p36.33

11q13.1

Type of geneprotein-codingprotein-coding
Descriptionagrinagrin proteoglycanbcl2-associated agonist of cell deathBCL-X/BCL-2 binding proteinBCL2-antagonist of cell death proteinBCL2-binding component 6BCL2-binding proteinbcl-2-binding component 6bcl-2-like protein 8bcl-XL/Bcl-2-associated death promoterbcl2 antagonist of
Modification date2020031520200327
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000379370, ENST00000477585, 
Fusion gene scores* DoF score14 X 7 X 10=9807 X 5 X 7=245
# samples 1810
** MAII scorelog2(18/980*10)=-2.4447848426729
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(10/245*10)=-1.29278174922785
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: AGRN [Title/Abstract] AND BAD [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointAGRN(957842)-BAD(64039275), # samples:4
Anticipated loss of major functional domain due to fusion event.AGRN-BAD 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.
AGRN-BAD 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.
AGRN-BAD 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.
AGRN-BAD 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.
* 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
HgeneAGRN

GO:0043113

receptor clustering

15340048

TgeneBAD

GO:0006915

apoptotic process

19667065

TgeneBAD

GO:0043065

positive regulation of apoptotic process

9388232

TgeneBAD

GO:0043280

positive regulation of cysteine-type endopeptidase activity involved in apoptotic process

18402937

TgeneBAD

GO:0045862

positive regulation of proteolysis

18387192

TgeneBAD

GO:0046931

pore complex assembly

19667065|21081150

TgeneBAD

GO:0071316

cellular response to nicotine

18676776

TgeneBAD

GO:0097202

activation of cysteine-type endopeptidase activity

18387192


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

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
ChimerDB4CESCTCGA-UC-A7PD-01AAGRNchr1

957842

-BADchr11

64039275

-
ChimerDB4CESCTCGA-UC-A7PD-01AAGRNchr1

957842

+BADchr11

64039275

-
ChimerDB4CESCTCGA-UC-A7PDAGRNchr1

957842

+BADchr11

64039275

-


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Fusion Gene ORF analysis for AGRN-BAD

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-intronENST00000379370ENST00000394531AGRNchr1

957842

+BADchr11

64039275

-
5CDS-intronENST00000379370ENST00000544785AGRNchr1

957842

+BADchr11

64039275

-
In-frameENST00000379370ENST00000309032AGRNchr1

957842

+BADchr11

64039275

-
In-frameENST00000379370ENST00000394532AGRNchr1

957842

+BADchr11

64039275

-
intron-3CDSENST00000477585ENST00000309032AGRNchr1

957842

+BADchr11

64039275

-
intron-3CDSENST00000477585ENST00000394532AGRNchr1

957842

+BADchr11

64039275

-
intron-intronENST00000477585ENST00000394531AGRNchr1

957842

+BADchr11

64039275

-
intron-intronENST00000477585ENST00000544785AGRNchr1

957842

+BADchr11

64039275

-

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)
ENST00000379370AGRNchr1957842+ENST00000394532BADchr1164039275-12125139252308
ENST00000379370AGRNchr1957842+ENST00000309032BADchr1164039275-12085139252308

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
ENST00000379370ENST00000394532AGRNchr1957842+BADchr1164039275-0.084132520.9158675
ENST00000379370ENST00000309032AGRNchr1957842+BADchr1164039275-0.0836541060.9163459

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Fusion Genomic Features for AGRN-BAD


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)

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.
genomic feature

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Fusion Protein Features for AGRN-BAD


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/chr1:957842/chr11:64039275)
- 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: 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: 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
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+23630_1571542046.0DomainNtA
TgeneBADchr1:957842chr11:64039275ENST0000030903214110_12462169.0MotifNote=BH3
TgeneBADchr1:957842chr11:64039275ENST0000039453203110_12462169.0MotifNote=BH3

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361941_20091542046.0Calcium bindingOntology_term=ECO:0000250
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361058_10971542046.0Compositional biasNote=Gly/Ser-rich
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361254_13241542046.0Compositional biasNote=Ser/Thr-rich
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236671_6771542046.0Compositional biasNote=Gly/Ser-rich
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236974_10991542046.0Compositional biasNote=Ser/Thr-rich
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361130_12521542046.0DomainSEA
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361329_13671542046.0DomainEGF-like 1
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361372_15481542046.0DomainLaminin G-like 1
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361549_15861542046.0DomainEGF-like 2
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361588_16251542046.0DomainEGF-like 3
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361635_18221542046.0DomainLaminin G-like 2
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361818_18571542046.0DomainEGF-like 4
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+2361868_20651542046.0DomainLaminin G-like 3
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236191_2441542046.0DomainKazal-like 1
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236264_3191542046.0DomainKazal-like 2
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236337_3911542046.0DomainKazal-like 3
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236408_4631542046.0DomainKazal-like 4
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236484_5361542046.0DomainKazal-like 5
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236540_6011542046.0DomainKazal-like 6
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236607_6661542046.0DomainKazal-like 7
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236699_7521542046.0DomainKazal-like 8
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236793_8461542046.0DomainLaminin EGF-like 1
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236847_8931542046.0DomainLaminin EGF-like 2
HgeneAGRNchr1:957842chr11:64039275ENST00000379370+236917_9711542046.0DomainKazal-like 9


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Fusion Gene Sequence for AGRN-BAD


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.
>2997_2997_1_AGRN-BAD_AGRN_chr1_957842_ENST00000379370_BAD_chr11_64039275_ENST00000309032_length(transcript)=1208nt_BP=513nt
CCCGTCCCCGGCGCGGCCCGCGCGCTCCTCCGCCGCCTCTCGCCTGCGCCATGGCCGGCCGGTCCCACCCGGGCCCGCTGCGGCCGCTGC
TGCCGCTCCTTGTGGTGGCCGCGTGCGTCCTGCCCGGAGCCGGCGGGACATGCCCGGAGCGCGCGCTGGAGCGGCGCGAGGAGGAGGCGA
ACGTGGTGCTCACCGGGACGGTGGAGGAGATCCTCAACGTGGACCCGGTGCAGCACACGTACTCCTGCAAGGTTCGGGTCTGGCGGTACT
TGAAGGGCAAAGACCTGGTGGCCCGGGAGAGCCTGCTGGACGGCGGCAACAAGGTGGTGATCAGCGGCTTTGGAGACCCCCTCATCTGTG
ACAACCAGGTGTCCACTGGGGACACCAGGATCTTCTTTGTGAACCCTGCACCCCCATACCTGTGGCCAGCCCACAAGAACGAGCTGATGC
TCAACTCCAGCCTCATGCGGATCACCCTGCGGAACCTGGAGGAGGTGGAGTTCTGTGTGGAAGGCGCTGGGGCTGTGGAGATCCGGAGTC
GCCACAGCTCCTACCCCGCGGGGACGGAGGACGACGAAGGGATGGGGGAGGAGCCCAGCCCCTTTCGGGGCCGCTCGCGCTCGGCGCCCC
CCAACCTCTGGGCAGCACAGCGCTATGGCCGCGAGCTCCGGAGGATGAGTGACGAGTTTGTGGACTCCTTTAAGAAGGGACTTCCTCGCC
CGAAGAGCGCGGGCACAGCAACGCAGATGCGGCAAAGCTCCAGCTGGACGCGAGTCTTCCAGTCCTGGTGGGATCGGAACTTGGGCAGGG
GAAGCTCCGCCCCCTCCCAGTGACCTTCGCTCCACATCCCGAAACTCCACCCGTTCCCACTGCCCTGGGCAGCCATCTTGAATATGGGCG
GAAGTACTTCCCTCAGGCCTATGCAAAAAGAGGATCCGTGCTGTCTCCTTTGGAGGGAGGGCTGACCCAGATTCCCTTCCGGTGCGTGTG
AAGCCACGGAAGGCTTGGTCCCATCGGAAGTTTTGGGTTTTCCGCCCACAGCCGCCGGAAGTGGCTCCGTGGCCCCGCCCTCAGGCTCCG
GGCTTTCCCCCAGGCGCCTGCGCTAAGTCGCGAGCCAGGTTTAACCGTTGCGTCACCGGGACCCGAGCCCCCGCGATGCCCTGGGGGCCG
TGCTCACTACCAAATGTTAATAAAGCCCGCGTCTGTGC

>2997_2997_1_AGRN-BAD_AGRN_chr1_957842_ENST00000379370_BAD_chr11_64039275_ENST00000309032_length(amino acids)=308AA_BP=1
MHRPEGSTSAHIQDGCPGQWERVEFRDVERRSLGGGGASPAQVPIPPGLEDSRPAGALPHLRCCARALRARKSLLKGVHKLVTHPPELAA
IALCCPEVGGRRARAAPKGAGLLPHPFVVLRPRGVGAVATPDLHSPSAFHTELHLLQVPQGDPHEAGVEHQLVLVGWPQVWGCRVHKEDP
GVPSGHLVVTDEGVSKAADHHLVAAVQQALPGHQVFALQVPPDPNLAGVRVLHRVHVEDLLHRPGEHHVRLLLAPLQRALRACPAGSGQD
ARGHHKERQQRPQRARVGPAGHGAGERRRRSARAAPGT

--------------------------------------------------------------
>2997_2997_2_AGRN-BAD_AGRN_chr1_957842_ENST00000379370_BAD_chr11_64039275_ENST00000394532_length(transcript)=1212nt_BP=513nt
CCCGTCCCCGGCGCGGCCCGCGCGCTCCTCCGCCGCCTCTCGCCTGCGCCATGGCCGGCCGGTCCCACCCGGGCCCGCTGCGGCCGCTGC
TGCCGCTCCTTGTGGTGGCCGCGTGCGTCCTGCCCGGAGCCGGCGGGACATGCCCGGAGCGCGCGCTGGAGCGGCGCGAGGAGGAGGCGA
ACGTGGTGCTCACCGGGACGGTGGAGGAGATCCTCAACGTGGACCCGGTGCAGCACACGTACTCCTGCAAGGTTCGGGTCTGGCGGTACT
TGAAGGGCAAAGACCTGGTGGCCCGGGAGAGCCTGCTGGACGGCGGCAACAAGGTGGTGATCAGCGGCTTTGGAGACCCCCTCATCTGTG
ACAACCAGGTGTCCACTGGGGACACCAGGATCTTCTTTGTGAACCCTGCACCCCCATACCTGTGGCCAGCCCACAAGAACGAGCTGATGC
TCAACTCCAGCCTCATGCGGATCACCCTGCGGAACCTGGAGGAGGTGGAGTTCTGTGTGGAAGGCGCTGGGGCTGTGGAGATCCGGAGTC
GCCACAGCTCCTACCCCGCGGGGACGGAGGACGACGAAGGGATGGGGGAGGAGCCCAGCCCCTTTCGGGGCCGCTCGCGCTCGGCGCCCC
CCAACCTCTGGGCAGCACAGCGCTATGGCCGCGAGCTCCGGAGGATGAGTGACGAGTTTGTGGACTCCTTTAAGAAGGGACTTCCTCGCC
CGAAGAGCGCGGGCACAGCAACGCAGATGCGGCAAAGCTCCAGCTGGACGCGAGTCTTCCAGTCCTGGTGGGATCGGAACTTGGGCAGGG
GAAGCTCCGCCCCCTCCCAGTGACCTTCGCTCCACATCCCGAAACTCCACCCGTTCCCACTGCCCTGGGCAGCCATCTTGAATATGGGCG
GAAGTACTTCCCTCAGGCCTATGCAAAAAGAGGATCCGTGCTGTCTCCTTTGGAGGGAGGGCTGACCCAGATTCCCTTCCGGTGCGTGTG
AAGCCACGGAAGGCTTGGTCCCATCGGAAGTTTTGGGTTTTCCGCCCACAGCCGCCGGAAGTGGCTCCGTGGCCCCGCCCTCAGGCTCCG
GGCTTTCCCCCAGGCGCCTGCGCTAAGTCGCGAGCCAGGTTTAACCGTTGCGTCACCGGGACCCGAGCCCCCGCGATGCCCTGGGGGCCG
TGCTCACTACCAAATGTTAATAAAGCCCGCGTCTGTGCCGCC

>2997_2997_2_AGRN-BAD_AGRN_chr1_957842_ENST00000379370_BAD_chr11_64039275_ENST00000394532_length(amino acids)=308AA_BP=1
MHRPEGSTSAHIQDGCPGQWERVEFRDVERRSLGGGGASPAQVPIPPGLEDSRPAGALPHLRCCARALRARKSLLKGVHKLVTHPPELAA
IALCCPEVGGRRARAAPKGAGLLPHPFVVLRPRGVGAVATPDLHSPSAFHTELHLLQVPQGDPHEAGVEHQLVLVGWPQVWGCRVHKEDP
GVPSGHLVVTDEGVSKAADHHLVAAVQQALPGHQVFALQVPPDPNLAGVRVLHRVHVEDLLHRPGEHHVRLLLAPLQRALRACPAGSGQD
ARGHHKERQQRPQRARVGPAGHGAGERRRRSARAAPGT

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

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Fusion Gene PPI Analysis for AGRN-BAD


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 AGRN-BAD


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 AGRN-BAD


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneAGRNC3808739MYASTHENIC SYNDROME, CONGENITAL, 83GENOMICS_ENGLAND;UNIPROT
HgeneAGRNC0751883Congenital Myasthenic Syndromes, Postsynaptic2CTD_human;ORPHANET
HgeneAGRNC0751884Congenital Myasthenic Syndromes, Presynaptic2CTD_human;ORPHANET
HgeneAGRNC0023467Leukemia, Myelocytic, Acute1CTD_human
HgeneAGRNC0026998Acute Myeloid Leukemia, M11CTD_human
HgeneAGRNC0751882Myasthenic Syndromes, Congenital1CTD_human;GENOMICS_ENGLAND
HgeneAGRNC1879321Acute Myeloid Leukemia (AML-M2)1CTD_human
TgeneC0033578Prostatic Neoplasms2CTD_human
TgeneC0376358Malignant neoplasm of prostate2CTD_human
TgeneC0007787Transient Ischemic Attack1CTD_human
TgeneC0023418leukemia1CTD_human
TgeneC0472381Posterior Circulation Transient Ischemic Attack1CTD_human
TgeneC0751019Carotid Circulation Transient Ischemic Attack1CTD_human
TgeneC0751020Transient Ischemic Attack, Vertebrobasilar Circulation1CTD_human
TgeneC0751021Crescendo Transient Ischemic Attacks1CTD_human
TgeneC0751022Brain Stem Ischemia, Transient1CTD_human
TgeneC0917805Transient Cerebral Ischemia1CTD_human
TgeneC1527335Transient Ischemic Attack, Anterior Circulation1CTD_human