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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:CASP7-C10orf137 (FusionGDB2 ID:13271)

Fusion Gene Summary for CASP7-C10orf137

check button Fusion gene summary
Fusion gene informationFusion gene name: CASP7-C10orf137
Fusion gene ID: 13271
HgeneTgene
Gene symbol

CASP7

C10orf137

Gene ID

840

26098

Gene namecaspase 7erythroid differentiation regulatory factor 1
SynonymsCASP-7|CMH-1|ICE-LAP3|LICE2|MCH3C10orf137
Cytomap

10q25.3

10q26.2

Type of geneprotein-codingprotein-coding
Descriptioncaspase-7ICE-like apoptotic protease 3apoptotic protease MCH-3caspase 7, apoptosis-related cysteine peptidasecaspase 7, apoptosis-related cysteine proteaseerythroid differentiation-related factor 1
Modification date2020032920200313
UniProtAcc

P55210

.
Ensembl transtripts involved in fusion geneENST00000369331, ENST00000369321, 
ENST00000345633, ENST00000369318, 
ENST00000369315, ENST00000452490, 
ENST00000468790, 
ENST00000356792, 
ENST00000337623, 
Fusion gene scores* DoF score8 X 6 X 6=2883 X 2 X 2=12
# samples 103
** MAII scorelog2(10/288*10)=-1.52606881166759
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: CASP7 [Title/Abstract] AND C10orf137 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointC10orf137(127409981)-CASP7(115457252), # samples:1
CASP7(115457362)-C10orf137(127426487), # samples:1
Anticipated loss of major functional domain due to fusion event.C10orf137-CASP7 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
CASP7-C10orf137 seems lost the major protein functional domain in Hgene 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
HgeneCASP7

GO:0006508

proteolysis

12888622

HgeneCASP7

GO:0006915

apoptotic process

17464193


check buttonFusion gene breakpoints across CASP7 (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 C10orf137 (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
ChimerDB4LUADTCGA-93-A4JQ-01ACASP7chr10

115457362

-C10orf137chr10

127426487

+


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Fusion Gene ORF analysis for CASP7-C10orf137

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-shiftENST00000369331ENST00000356792CASP7chr10

115457362

-C10orf137chr10

127426487

+
Frame-shiftENST00000369331ENST00000337623CASP7chr10

115457362

-C10orf137chr10

127426487

+
Frame-shiftENST00000369321ENST00000356792CASP7chr10

115457362

-C10orf137chr10

127426487

+
Frame-shiftENST00000369321ENST00000337623CASP7chr10

115457362

-C10orf137chr10

127426487

+
Frame-shiftENST00000345633ENST00000356792CASP7chr10

115457362

-C10orf137chr10

127426487

+
Frame-shiftENST00000345633ENST00000337623CASP7chr10

115457362

-C10orf137chr10

127426487

+
Frame-shiftENST00000369318ENST00000356792CASP7chr10

115457362

-C10orf137chr10

127426487

+
Frame-shiftENST00000369318ENST00000337623CASP7chr10

115457362

-C10orf137chr10

127426487

+
Frame-shiftENST00000369315ENST00000356792CASP7chr10

115457362

-C10orf137chr10

127426487

+
Frame-shiftENST00000369315ENST00000337623CASP7chr10

115457362

-C10orf137chr10

127426487

+
intron-3CDSENST00000452490ENST00000356792CASP7chr10

115457362

-C10orf137chr10

127426487

+
intron-3CDSENST00000452490ENST00000337623CASP7chr10

115457362

-C10orf137chr10

127426487

+
intron-3CDSENST00000468790ENST00000356792CASP7chr10

115457362

-C10orf137chr10

127426487

+
intron-3CDSENST00000468790ENST00000337623CASP7chr10

115457362

-C10orf137chr10

127426487

+

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 CASP7-C10orf137


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 CASP7-C10orf137


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
CASP7

P55210

.
FUNCTION: Involved in the activation cascade of caspases responsible for apoptosis execution. Cleaves and activates sterol regulatory element binding proteins (SREBPs). Proteolytically cleaves poly(ADP-ribose) polymerase (PARP) at a '216-Asp-|-Gly-217' bond. Overexpression promotes programmed cell death.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.
- 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 CASP7-C10orf137


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 CASP7-C10orf137


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 CASP7-C10orf137


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 CASP7-C10orf137


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCASP7C0006142Malignant neoplasm of breast1CTD_human
HgeneCASP7C0023467Leukemia, Myelocytic, Acute1CTD_human
HgeneCASP7C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneCASP7C0026998Acute Myeloid Leukemia, M11CTD_human
HgeneCASP7C0027055Myocardial Reperfusion Injury1CTD_human
HgeneCASP7C0042900Vitiligo1CTD_human
HgeneCASP7C0678222Breast Carcinoma1CTD_human
HgeneCASP7C1257931Mammary Neoplasms, Human1CTD_human
HgeneCASP7C1458155Mammary Neoplasms1CTD_human
HgeneCASP7C1879321Acute Myeloid Leukemia (AML-M2)1CTD_human
HgeneCASP7C4704874Mammary Carcinoma, Human1CTD_human