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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:CDH12-HSPD1 (FusionGDB2 ID:15051)

Fusion Gene Summary for CDH12-HSPD1

check button Fusion gene summary
Fusion gene informationFusion gene name: CDH12-HSPD1
Fusion gene ID: 15051
HgeneTgene
Gene symbol

CDH12

HSPD1

Gene ID

1010

3329

Gene namecadherin 12heat shock protein family D (Hsp60) member 1
SynonymsCDHBCPN60|GROEL|HLD4|HSP-60|HSP60|HSP65|HuCHA60|SPG13
Cytomap

5p14.3

2q33.1

Type of geneprotein-codingprotein-coding
Descriptioncadherin-12Br-cadherinN-cadherin 2brain-cadherincadherin, neural type, 2neural type cadherin 2neuronal cadherin 260 kDa heat shock protein, mitochondrial60 kDa chaperoninP60 lymphocyte proteinchaperonin 60epididymis secretory sperm binding proteinheat shock 60kDa protein 1 (chaperonin)heat shock protein 65mitochondrial matrix protein P1short heat shock prote
Modification date2020031320200315
UniProtAcc.

P10809

Ensembl transtripts involved in fusion geneENST00000504376, ENST00000382254, 
ENST00000522262, ENST00000521384, 
ENST00000388968, ENST00000345042, 
ENST00000544407, 
Fusion gene scores* DoF score9 X 9 X 3=24314 X 10 X 6=840
# samples 916
** MAII scorelog2(9/243*10)=-1.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/840*10)=-2.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CDH12 [Title/Abstract] AND HSPD1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCDH12(21884875)-HSPD1(198351924), # 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
TgeneHSPD1

GO:0002368

B cell cytokine production

16148103

TgeneHSPD1

GO:0002755

MyD88-dependent toll-like receptor signaling pathway

16148103

TgeneHSPD1

GO:0002842

positive regulation of T cell mediated immune response to tumor cell

10663613

TgeneHSPD1

GO:0006919

activation of cysteine-type endopeptidase activity involved in apoptotic process

17823127

TgeneHSPD1

GO:0006986

response to unfolded protein

11050098

TgeneHSPD1

GO:0032727

positive regulation of interferon-alpha production

17164250

TgeneHSPD1

GO:0032729

positive regulation of interferon-gamma production

17164250

TgeneHSPD1

GO:0032733

positive regulation of interleukin-10 production

16148103

TgeneHSPD1

GO:0032735

positive regulation of interleukin-12 production

17164250

TgeneHSPD1

GO:0032755

positive regulation of interleukin-6 production

16148103

TgeneHSPD1

GO:0042026

protein refolding

11050098

TgeneHSPD1

GO:0042100

B cell proliferation

16148103

TgeneHSPD1

GO:0042110

T cell activation

15371451|17164250|18256040

TgeneHSPD1

GO:0042113

B cell activation

16148103

TgeneHSPD1

GO:0043032

positive regulation of macrophage activation

17164250

TgeneHSPD1

GO:0044406

adhesion of symbiont to host

20633027

TgeneHSPD1

GO:0048291

isotype switching to IgG isotypes

16148103

TgeneHSPD1

GO:0050870

positive regulation of T cell activation

16148103|17164250


check buttonFusion gene breakpoints across CDH12 (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 HSPD1 (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
ChiTaRS5.0N/ADT220072CDH12chr5

21884875

+HSPD1chr2

198351924

-


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Fusion Gene ORF analysis for CDH12-HSPD1

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
intron-3CDSENST00000504376ENST00000388968CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-3CDSENST00000504376ENST00000345042CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-intronENST00000504376ENST00000544407CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-3CDSENST00000382254ENST00000388968CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-3CDSENST00000382254ENST00000345042CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-intronENST00000382254ENST00000544407CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-3CDSENST00000522262ENST00000388968CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-3CDSENST00000522262ENST00000345042CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-intronENST00000522262ENST00000544407CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-3CDSENST00000521384ENST00000388968CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-3CDSENST00000521384ENST00000345042CDH12chr5

21884875

+HSPD1chr2

198351924

-
intron-intronENST00000521384ENST00000544407CDH12chr5

21884875

+HSPD1chr2

198351924

-

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 CDH12-HSPD1


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 CDH12-HSPD1


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
.HSPD1

P10809

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: Chaperonin implicated in mitochondrial protein import and macromolecular assembly. Together with Hsp10, facilitates the correct folding of imported proteins. May also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix (PubMed:1346131, PubMed:11422376). The functional units of these chaperonins consist of heptameric rings of the large subunit Hsp60, which function as a back-to-back double ring. In a cyclic reaction, Hsp60 ring complexes bind one unfolded substrate protein per ring, followed by the binding of ATP and association with 2 heptameric rings of the co-chaperonin Hsp10. This leads to sequestration of the substrate protein in the inner cavity of Hsp60 where, for a certain period of time, it can fold undisturbed by other cell components. Synchronous hydrolysis of ATP in all Hsp60 subunits results in the dissociation of the chaperonin rings and the release of ADP and the folded substrate protein (Probable). {ECO:0000269|PubMed:11422376, ECO:0000269|PubMed:1346131, ECO:0000305|PubMed:25918392}.

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 CDH12-HSPD1


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 CDH12-HSPD1


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 CDH12-HSPD1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneHSPD1P10809DB09130CopperSmall moleculeApproved|Investigational
TgeneHSPD1P10809DB09130CopperSmall moleculeApproved|Investigational

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Related Diseases for CDH12-HSPD1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCDH12C0001973Alcoholic Intoxication, Chronic2PSYGENET
HgeneCDH12C0033578Prostatic Neoplasms1CTD_human
HgeneCDH12C0376358Malignant neoplasm of prostate1CTD_human
TgeneHSPD1C1854467Spastic paraplegia 13, autosomal dominant4CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneHSPD1C2677109Leukodystrophy, Hypomyelinating, 44CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneHSPD1C0024623Malignant neoplasm of stomach2CTD_human
TgeneHSPD1C0038356Stomach Neoplasms2CTD_human
TgeneHSPD1C1708349Hereditary Diffuse Gastric Cancer2CTD_human
TgeneHSPD1C0001418Adenocarcinoma1CTD_human
TgeneHSPD1C0007134Renal Cell Carcinoma1CTD_human
TgeneHSPD1C0007194Hypertrophic Cardiomyopathy1CTD_human
TgeneHSPD1C0019693HIV Infections1CTD_human
TgeneHSPD1C0033141Cardiomyopathies, Primary1CTD_human
TgeneHSPD1C0036529Myocardial Diseases, Secondary1CTD_human
TgeneHSPD1C0205641Adenocarcinoma, Basal Cell1CTD_human
TgeneHSPD1C0205642Adenocarcinoma, Oxyphilic1CTD_human
TgeneHSPD1C0205643Carcinoma, Cribriform1CTD_human
TgeneHSPD1C0205644Carcinoma, Granular Cell1CTD_human
TgeneHSPD1C0205645Adenocarcinoma, Tubular1CTD_human
TgeneHSPD1C0238281Middle Cerebral Artery Syndrome1CTD_human
TgeneHSPD1C0279702Conventional (Clear Cell) Renal Cell Carcinoma1CTD_human
TgeneHSPD1C0376618Endotoxemia1CTD_human
TgeneHSPD1C0740376Middle Cerebral Artery Thrombosis1CTD_human
TgeneHSPD1C0740391Middle Cerebral Artery Occlusion1CTD_human
TgeneHSPD1C0740392Infarction, Middle Cerebral Artery1CTD_human
TgeneHSPD1C0751845Middle Cerebral Artery Embolus1CTD_human
TgeneHSPD1C0751846Left Middle Cerebral Artery Infarction1CTD_human
TgeneHSPD1C0751847Embolic Infarction, Middle Cerebral Artery1CTD_human
TgeneHSPD1C0751848Thrombotic Infarction, Middle Cerebral Artery1CTD_human
TgeneHSPD1C0751849Right Middle Cerebral Artery Infarction1CTD_human
TgeneHSPD1C0878544Cardiomyopathies1CTD_human
TgeneHSPD1C0948089Acute Coronary Syndrome1CTD_human
TgeneHSPD1C1266042Chromophobe Renal Cell Carcinoma1CTD_human
TgeneHSPD1C1266043Sarcomatoid Renal Cell Carcinoma1CTD_human
TgeneHSPD1C1266044Collecting Duct Carcinoma of the Kidney1CTD_human
TgeneHSPD1C1306837Papillary Renal Cell Carcinoma1CTD_human
TgeneHSPD1C4505456HIV Coinfection1CTD_human
TgeneHSPD1C4551472Hypertrophic obstructive cardiomyopathy1CTD_human