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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:CAPN2-SH2D1B

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CAPN2-SH2D1B
FusionPDB ID: 12877
FusionGDB2.0 ID: 12877
HgeneTgene
Gene symbol

CAPN2

SH2D1B

Gene ID

824

117157

Gene namecalpain 2SH2 domain containing 1B
SynonymsCANP2|CANPL2|CANPml|mCANPEAT2
Cytomap

1q41

1q23.3

Type of geneprotein-codingprotein-coding
Descriptioncalpain-2 catalytic subunitCANP 2M-calpaincalcium-activated neutral proteinase 2calpain 2, (m/II) large subunitcalpain 2, large [catalytic] subunitcalpain 2, large subunitcalpain M-typecalpain, large polypeptide L2millimolar-calpainSH2 domain-containing protein 1BEAT-2EWS/FLI1-activated transcript 2SH2 domain-containing molecule EAT2
Modification date2020031320200313
UniProtAcc

P17655

.
Ensembl transtripts involved in fusion geneENST idsENST00000474026, ENST00000295006, 
ENST00000433674, 
ENST00000367929, 
ENST00000359567, ENST00000493550, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 9 X 5=4954 X 4 X 3=48
# samples 114
** MAII scorelog2(11/495*10)=-2.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: CAPN2 [Title/Abstract] AND SH2D1B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CAPN2(223954118)-SH2D1B(162368877), # samples:2
Anticipated loss of major functional domain due to fusion event.CAPN2-SH2D1B 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.
CAPN2-SH2D1B 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.
CAPN2-SH2D1B 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.
CAPN2-SH2D1B 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
HgeneCAPN2

GO:0051603

proteolysis involved in cellular protein catabolic process

12150984


check buttonFusion gene breakpoints across CAPN2 (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 SH2D1B (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
ChimerDB4SKCMTCGA-EE-A182-06ACAPN2chr1

223954118

+SH2D1Bchr1

162368877

-


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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)
ENST00000433674CAPN2chr1223954118+ENST00000367929SH2D1Bchr1162368877-392217072271696489
ENST00000295006CAPN2chr1223954118+ENST00000367929SH2D1Bchr1162368877-422920143092003564

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
ENST00000433674ENST00000367929CAPN2chr1223954118+SH2D1Bchr1162368877-0.0007984730.9992016
ENST00000295006ENST00000367929CAPN2chr1223954118+SH2D1Bchr1162368877-0.0006674860.9993325

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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

>12877_12877_1_CAPN2-SH2D1B_CAPN2_chr1_223954118_ENST00000295006_SH2D1B_chr1_162368877_ENST00000367929_length(amino acids)=564AA_BP=
MAGIAAKLAKDREAAEGLGSHDRAIKYLNQDYEALRNECLEAGTLFQDPSFPAIPSALGFKELGPYSSKTRGIEWKRPTEICADPQFIIG
GATRTDICQGALGDCWLLAAIASLTLNEEILARVVPLNQSFQENYAGIFHFQFWQYGEWVEVVVDDRLPTKDGELLFVHSAEGSEFWSAL
LEKAYAKINGCYEALSGGATTEGFEDFTGGIAEWYELKKPPPNLFKIIQKALQKGSLLGCSIDITSAADSEAITFQKLVKGHAYSVTGAE
EVESNGSLQKLIRIRNPWGEVEWTGRWNDNCPSWNTIDPEERERLTRRHEDGEFWMSFSDFLRHYSRLEICNLTPDTLTSDTYKKWKLTK
MDGNWRRGSTAGGCRNYPNTFWMNPQYLIKLEEEDEDEEDGESGCTFLVGLIQKHRRRQRKMGEDMHTIGFGIYEVPEELSGQTNIHLSK
NFFLTNRARERSDTFINLREVLNRFKLPPGEYILVPSTFEPNKDGDFCIRVFSEKKADYQAVDDEIEANLEEFDISEDDIDDGFRRLFAQ

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

>12877_12877_2_CAPN2-SH2D1B_CAPN2_chr1_223954118_ENST00000433674_SH2D1B_chr1_162368877_ENST00000367929_length(amino acids)=489AA_BP=
MANMEICADPQFIIGGATRTDICQGALGDCWLLAAIASLTLNEEILARVVPLNQSFQENYAGIFHFQFWQYGEWVEVVVDDRLPTKDGEL
LFVHSAEGSEFWSALLEKAYAKINGCYEALSGGATTEGFEDFTGGIAEWYELKKPPPNLFKIIQKALQKGSLLGCSIDITSAADSEAITF
QKLVKGHAYSVTGAEEVESNGSLQKLIRIRNPWGEVEWTGRWNDNCPSWNTIDPEERERLTRRHEDGEFWMSFSDFLRHYSRLEICNLTP
DTLTSDTYKKWKLTKMDGNWRRGSTAGGCRNYPNTFWMNPQYLIKLEEEDEDEEDGESGCTFLVGLIQKHRRRQRKMGEDMHTIGFGIYE
VPEELSGQTNIHLSKNFFLTNRARERSDTFINLREVLNRFKLPPGEYILVPSTFEPNKDGDFCIRVFSEKKADYQAVDDEIEANLEEFDI

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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/chr1:223954118/chr1:162368877)
- 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
CAPN2

P17655

.
FUNCTION: Calcium-regulated non-lysosomal thiol-protease which catalyzes limited proteolysis of substrates involved in cytoskeletal remodeling and signal transduction. Proteolytically cleaves MYOC at 'Arg-226' (PubMed:17650508). Proteolytically cleaves CPEB3 following neuronal stimulation which abolishes CPEB3 translational repressor activity, leading to translation of CPEB3 target mRNAs (By similarity). {ECO:0000250|UniProtKB:O08529, ECO:0000269|PubMed:17650508}.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
TgeneSH2D1Bchr1:223954118chr1:162368877ENST00000359567035_101078.0DomainSH2

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCAPN2chr1:223954118chr1:162368877ENST00000295006+121585_5960701.0Calcium bindingNote=1
HgeneCAPN2chr1:223954118chr1:162368877ENST00000295006+121615_6260701.0Calcium bindingNote=2
HgeneCAPN2chr1:223954118chr1:162368877ENST00000433674+121585_5960623.0Calcium bindingNote=1
HgeneCAPN2chr1:223954118chr1:162368877ENST00000433674+121615_6260623.0Calcium bindingNote=2
HgeneCAPN2chr1:223954118chr1:162368877ENST00000295006+12145_3440701.0DomainCalpain catalytic
HgeneCAPN2chr1:223954118chr1:162368877ENST00000295006+121572_6050701.0DomainEF-hand 1
HgeneCAPN2chr1:223954118chr1:162368877ENST00000295006+121602_6370701.0DomainEF-hand 2
HgeneCAPN2chr1:223954118chr1:162368877ENST00000295006+121667_7000701.0DomainEF-hand 3
HgeneCAPN2chr1:223954118chr1:162368877ENST00000433674+12145_3440623.0DomainCalpain catalytic
HgeneCAPN2chr1:223954118chr1:162368877ENST00000433674+121572_6050623.0DomainEF-hand 1
HgeneCAPN2chr1:223954118chr1:162368877ENST00000433674+121602_6370623.0DomainEF-hand 2
HgeneCAPN2chr1:223954118chr1:162368877ENST00000433674+121667_7000623.0DomainEF-hand 3
HgeneCAPN2chr1:223954118chr1:162368877ENST00000295006+121345_5140701.0RegionNote=Domain III
HgeneCAPN2chr1:223954118chr1:162368877ENST00000295006+121515_5290701.0RegionNote=Linker
HgeneCAPN2chr1:223954118chr1:162368877ENST00000295006+121530_7000701.0RegionNote=Domain IV
HgeneCAPN2chr1:223954118chr1:162368877ENST00000433674+121345_5140623.0RegionNote=Domain III
HgeneCAPN2chr1:223954118chr1:162368877ENST00000433674+121515_5290623.0RegionNote=Linker
HgeneCAPN2chr1:223954118chr1:162368877ENST00000433674+121530_7000623.0RegionNote=Domain IV
TgeneSH2D1Bchr1:223954118chr1:162368877ENST00000367929145_10166.0133.0DomainSH2


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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
CAPN2
SH2D1B


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 CAPN2-SH2D1B


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 CAPN2-SH2D1B


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