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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:TSC22D2-ADCY5 (FusionGDB2 ID:93856)

Fusion Gene Summary for TSC22D2-ADCY5

check button Fusion gene summary
Fusion gene informationFusion gene name: TSC22D2-ADCY5
Fusion gene ID: 93856
HgeneTgene
Gene symbol

TSC22D2

ADCY5

Gene ID

9819

111

Gene nameTSC22 domain family member 2adenylate cyclase 5
SynonymsTILZ4a|TILZ4b|TILZ4cAC5|FDFM
Cytomap

3q25.1

3q21.1

Type of geneprotein-codingprotein-coding
DescriptionTSC22 domain family protein 2TSC22 domain family 2TSC22-related-inducible leucine zipper protein 4adenylate cyclase type 5ATP pyrophosphate-lyase 5adenylate cyclase type Vadenylyl cyclase 5epididymis secretory sperm binding protein
Modification date2020031320200313
UniProtAcc.

O95622

Ensembl transtripts involved in fusion geneENST00000361136, ENST00000361875, 
ENST00000492828, 
ENST00000462833, 
ENST00000491190, ENST00000309879, 
ENST00000470367, 
Fusion gene scores* DoF score6 X 3 X 6=1086 X 6 X 3=108
# samples 77
** MAII scorelog2(7/108*10)=-0.625604485218502
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/108*10)=-0.625604485218502
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TSC22D2 [Title/Abstract] AND ADCY5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTSC22D2(150129095)-ADCY5(123071428), # samples:2
Anticipated loss of major functional domain due to fusion event.TSC22D2-ADCY5 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
TSC22D2-ADCY5 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
TSC22D2-ADCY5 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
TSC22D2-ADCY5 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
TgeneADCY5

GO:0006171

cAMP biosynthetic process

15385642|24700542

TgeneADCY5

GO:1904322

cellular response to forskolin

15385642|24700542


check buttonFusion gene breakpoints across TSC22D2 (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 ADCY5 (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
ChimerDB4LUSCTCGA-85-6175-01ATSC22D2chr3

150129095

+ADCY5chr3

123071428

-
ChimerDB4LUSCTCGA-85-6175-01ATSC22D2chr3

150129095

-ADCY5chr3

123071428

-


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Fusion Gene ORF analysis for TSC22D2-ADCY5

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
Frame-shiftENST00000361136ENST00000462833TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
Frame-shiftENST00000361136ENST00000491190TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
Frame-shiftENST00000361136ENST00000309879TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
5CDS-5UTRENST00000361136ENST00000470367TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
Frame-shiftENST00000361875ENST00000462833TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
Frame-shiftENST00000361875ENST00000491190TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
Frame-shiftENST00000361875ENST00000309879TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
5CDS-5UTRENST00000361875ENST00000470367TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
intron-3CDSENST00000492828ENST00000462833TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
intron-3CDSENST00000492828ENST00000491190TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
intron-3CDSENST00000492828ENST00000309879TSC22D2chr3

150129095

+ADCY5chr3

123071428

-
intron-5UTRENST00000492828ENST00000470367TSC22D2chr3

150129095

+ADCY5chr3

123071428

-

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 TSC22D2-ADCY5


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.

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 TSC22D2-ADCY5


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
.ADCY5

O95622

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: Catalyzes the formation of the signaling molecule cAMP in response to G-protein signaling (PubMed:15385642, PubMed:26206488, PubMed:24700542). Mediates signaling downstream of ADRB1 (PubMed:24700542). Regulates the increase of free cytosolic Ca(2+) in response to increased blood glucose levels and contributes to the regulation of Ca(2+)-dependent insulin secretion (PubMed:24740569). {ECO:0000269|PubMed:15385642, ECO:0000269|PubMed:24700542, ECO:0000269|PubMed:24740569, ECO:0000269|PubMed:26206488}.

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 TSC22D2-ADCY5


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 TSC22D2-ADCY5


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 TSC22D2-ADCY5


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneADCY5O95622DB09121AurothioglucoseSmall moleculeApproved|Withdrawn

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Related Diseases for TSC22D2-ADCY5


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneADCY5C1847627Dyskinesia, Familial, with Facial Myokymia4CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneADCY5C0011570Mental Depression2PSYGENET
TgeneADCY5C0011581Depressive disorder2PSYGENET
TgeneADCY5C0011860Diabetes Mellitus, Non-Insulin-Dependent2CTD_human
TgeneADCY5C0033141Cardiomyopathies, Primary2CTD_human
TgeneADCY5C0036529Myocardial Diseases, Secondary2CTD_human
TgeneADCY5C0878544Cardiomyopathies2CTD_human
TgeneADCY5C0001787Osteoporosis, Age-Related1CTD_human
TgeneADCY5C0001973Alcoholic Intoxication, Chronic1PSYGENET
TgeneADCY5C0005612Birth Weight1CTD_human
TgeneADCY5C0007097Carcinoma1CTD_human
TgeneADCY5C0013421Dystonia1GENOMICS_ENGLAND
TgeneADCY5C0016059Fibrosis1CTD_human
TgeneADCY5C0020538Hypertensive disease1CTD_human
TgeneADCY5C0024667Animal Mammary Neoplasms1CTD_human
TgeneADCY5C0024668Mammary Neoplasms, Experimental1CTD_human
TgeneADCY5C0029456Osteoporosis1CTD_human
TgeneADCY5C0029459Osteoporosis, Senile1CTD_human
TgeneADCY5C0041696Unipolar Depression1PSYGENET
TgeneADCY5C0205696Anaplastic carcinoma1CTD_human
TgeneADCY5C0205697Carcinoma, Spindle-Cell1CTD_human
TgeneADCY5C0205698Undifferentiated carcinoma1CTD_human
TgeneADCY5C0205699Carcinomatosis1CTD_human
TgeneADCY5C0242698Ventricular Dysfunction, Left1CTD_human
TgeneADCY5C0393584Benign Hereditary Chorea1ORPHANET
TgeneADCY5C0751406Post-Traumatic Osteoporosis1CTD_human
TgeneADCY5C1257925Mammary Carcinoma, Animal1CTD_human
TgeneADCY5C1269683Major Depressive Disorder1PSYGENET
TgeneADCY5C1535926Neurodevelopmental Disorders1CTD_human
TgeneADCY5C1623038Cirrhosis1CTD_human
TgeneADCY5C1859098Chorea, Benign Familial1ORPHANET