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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:JAG1-INPP5A

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: JAG1-INPP5A
FusionPDB ID: 40823
FusionGDB2.0 ID: 40823
HgeneTgene
Gene symbol

JAG1

INPP5A

Gene ID

182

3632

Gene namejagged canonical Notch ligand 1inositol polyphosphate-5-phosphatase A
SynonymsAGS|AGS1|AHD|AWS|CD339|DCHE|HJ1|JAGL15PTASE
Cytomap

20p12.2

10q26.3

Type of geneprotein-codingprotein-coding
Descriptionprotein jagged-1inositol polyphosphate-5-phosphatase A43 kDa inositol polyphosphate 5-phophatase43 kDa inositol polyphosphate 5-phosphataseCTCL tumor antigen HD-CL-02InsP3 5-phosphataseinositol polyphosphate-5-phosphatase, 40kDinositol polyphosphate-5-phosphatase,
Modification date2020031320200313
UniProtAcc

P78504

Q14642

Ensembl transtripts involved in fusion geneENST idsENST00000254958, ENST00000423891, 
ENST00000488480, 
ENST00000487614, 
ENST00000368593, ENST00000368594, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 7 X 5=2458 X 8 X 3=192
# samples 78
** MAII scorelog2(7/245*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(8/192*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: JAG1 [Title/Abstract] AND INPP5A [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)JAG1(10653348)-INPP5A(134421418), # samples:1
Anticipated loss of major functional domain due to fusion event.JAG1-INPP5A 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.
JAG1-INPP5A 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
HgeneJAG1

GO:0001953

negative regulation of cell-matrix adhesion

11549580

HgeneJAG1

GO:0022408

negative regulation of cell-cell adhesion

11549580

HgeneJAG1

GO:0030336

negative regulation of cell migration

11549580

TgeneINPP5A

GO:0046855

inositol phosphate dephosphorylation

8006039


check buttonFusion gene breakpoints across JAG1 (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 INPP5A (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
ChimerDB4COADTCGA-A6-2685JAG1chr20

10653348

-INPP5Achr10

134421418

+


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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)
ENST00000254958JAG1chr2010653348-ENST00000368594INPP5Achr10134421418+35139035162066516
ENST00000254958JAG1chr2010653348-ENST00000368593INPP5Achr10134421418+20129035161991491

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
ENST00000254958ENST00000368594JAG1chr2010653348-INPP5Achr10134421418+0.0005469790.999453
ENST00000254958ENST00000368593JAG1chr2010653348-INPP5Achr10134421418+0.0024006290.9975994

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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

>40823_40823_1_JAG1-INPP5A_JAG1_chr20_10653348_ENST00000254958_INPP5A_chr10_134421418_ENST00000368593_length(amino acids)=491AA_BP=129
MRSPRTRGRSGRPLSLLLALLCALRAKVCGASGQFELEILSMQNVNGELQNGNCCGGARNPGDRKCTRDECDTYFKVCLKEYQSRVTAGG
PCSFGSGSTPVIGGNTFNLKASRGNDRNRIVLPFSFAWPPENLQKNWLREFYQVVHTHKPHFMALHCQEFGGKNYEASMSHVDKFVKELL
SSDAMKEYNRARVYLDENYKSQEHFTALGSFYFLHESLKNIYQFDFKAKKYRKVAGKEIYSDTLESTPMLEKEKFPQDYFPECKWSRKGF
IRTRWCIADCAFDLVNIHLFHDASNLVAWETSPSVYSGIRHKALGYVLDRIIDQRFEKVSYFVFGDFNFRLDSKSVVETLCTKATMQTVR
AADTNEVVKLIFRESDNDRKVMLQLEKKLFDYFNQEVFRDNNGTALLEFDKELSVFKDRLYELDISFPPSYPYSEDARQGEQYMNTRCPA

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

>40823_40823_2_JAG1-INPP5A_JAG1_chr20_10653348_ENST00000254958_INPP5A_chr10_134421418_ENST00000368594_length(amino acids)=516AA_BP=129
MRSPRTRGRSGRPLSLLLALLCALRAKVCGASGQFELEILSMQNVNGELQNGNCCGGARNPGDRKCTRDECDTYFKVCLKEYQSRVTAGG
PCSFGSGSTPVIGGNTFNLKASRGNDRNRIVLPFSFAWPPENLQKNWLREFYQVVHTHKPHFMALHCQEFGGKNYEASMSHVDKFVKELL
SSDAMKEYNRARVYLDENYKSQEHFTALGSFYFLHESLKNIYQFDFKAKKYRKVAGKEIYSDTLESTPMLEKEKFPQDYFPECKWSRKGF
IRTRWCIADCAFDLVNIHLFHDASNLVAWETSPSVYSGIRHKALGYVLDRIIDQRFEKVSYFVFGDFNFRLDSKSVVETLCTKATMQTVR
AADTNEVVKLIFRESDNDRKVMLQLEKKLFDYFNQEVFRDNNGTALLEFDKELSVFKDRLYELDISFPPSYPYSEDARQGEQYMNTRCPA

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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/chr20:10653348/chr10:134421418)
- 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
JAG1

P78504

INPP5A

Q14642

FUNCTION: Ligand for multiple Notch receptors and involved in the mediation of Notch signaling (PubMed:18660822, PubMed:20437614). May be involved in cell-fate decisions during hematopoiesis (PubMed:9462510). Seems to be involved in early and late stages of mammalian cardiovascular development. Inhibits myoblast differentiation (By similarity). Enhances fibroblast growth factor-induced angiogenesis (in vitro). {ECO:0000250, ECO:0000269|PubMed:18660822, ECO:0000269|PubMed:20437614, ECO:0000269|PubMed:9462510}.FUNCTION: Phosphatase that specifically hydrolyzes the 5-phosphate of inositol 1,4,5-trisphosphate to inositol 1,4-bisphosphate, and inositol 1,3,4,5-tetrasphosphate to inositol 1,3,4-trisphosphate (PubMed:8013665, PubMed:8769125, PubMed:8626616). Plays a crucial role in the survival of cerebellar Purkinje cells (By similarity). {ECO:0000250|UniProtKB:Q7TNC9, ECO:0000269|PubMed:8013665, ECO:0000269|PubMed:8626616, ECO:0000269|PubMed:8769125}.

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

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226185_229129.01219.0DomainDSL
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226230_263129.01219.0DomainEGF-like 1
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226264_294129.01219.0DomainEGF-like 2%3B atypical
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226296_334129.01219.0DomainEGF-like 3
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226336_372129.01219.0DomainEGF-like 4
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226374_410129.01219.0DomainEGF-like 5%3B calcium-binding
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226412_448129.01219.0DomainEGF-like 6%3B calcium-binding
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226450_485129.01219.0DomainEGF-like 7%3B calcium-binding
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226487_523129.01219.0DomainEGF-like 8%3B calcium-binding
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226525_561129.01219.0DomainEGF-like 9
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226586_627129.01219.0DomainEGF-like 10
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226629_665129.01219.0DomainEGF-like 11%3B calcium-binding
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226667_703129.01219.0DomainEGF-like 12%3B calcium-binding
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226705_741129.01219.0DomainEGF-like 13
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226744_780129.01219.0DomainEGF-like 14
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226782_818129.01219.0DomainEGF-like 15%3B calcium-binding
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-226820_856129.01219.0DomainEGF-like 16%3B calcium-binding
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-2261094_1218129.01219.0Topological domainCytoplasmic
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-22634_1067129.01219.0Topological domainExtracellular
HgeneJAG1chr20:10653348chr10:134421418ENST00000254958-2261068_1093129.01219.0TransmembraneHelical


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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
JAG1
INPP5A


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 JAG1-INPP5A


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 JAG1-INPP5A


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