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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 18002

FusionGeneSummary for JAG1_SLX4IP

check button Fusion gene summary
Fusion gene informationFusion gene name: JAG1_SLX4IP
Fusion gene ID: 18002
HgeneTgene
Gene symbol

JAG1

SLX4IP

Gene ID

182

128710

Gene namejagged 1SLX4 interacting protein
SynonymsAGS|AGS1|AHD|AWS|CD339|HJ1|JAGL1C20orf94|bA204H22.1|bA254M13.1|dJ1099D15.3
Cytomap

20p12.2

20p12.2

Type of geneprotein-codingprotein-coding
Descriptionprotein jagged-1protein SLX4IP
Modification date2018052220180519
UniProtAcc

P78504

Q5VYV7

Ensembl transtripts involved in fusion geneENST00000254958, ENST00000423891, 
ENST00000488480, 
ENST00000334534, 
Fusion gene scores* DoF score3 X 3 X 2=182 X 2 X 2=8
# samples 32
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/8*10)=1.32192809488736
Context

PubMed: JAG1 [Title/Abstract] AND SLX4IP [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGALDCESCTCGA-MY-A5BE-01AJAG1chr20

10622108

-SLX4IPchr20

10582379

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-shiftENST00000254958ENST00000334534JAG1chr20

10622108

-SLX4IPchr20

10582379

+
In-frameENST00000423891ENST00000334534JAG1chr20

10622108

-SLX4IPchr20

10582379

+
intron-3CDSENST00000488480ENST00000334534JAG1chr20

10622108

-SLX4IPchr20

10582379

+

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FusionProtFeatures for JAG1_SLX4IP


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
JAG1

P78504

SLX4IP

Q5VYV7

Ligand for multiple Notch receptors and involved in themediation of Notch signaling. May be involved in cell-fatedecisions during hematopoiesis. Seems to be involved in early andlate stages of mammalian cardiovascular development. Inhibitsmyoblast differentiation (By similarity). Enhances fibroblastgrowth factor-induced angiogenesis (in vitro). {ECO:0000250,ECO:0000269|PubMed:18660822, ECO:0000269|PubMed:9462510}.

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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FusionGeneSequence for JAG1_SLX4IP


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for JAG1_SLX4IP


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
JAG1NOTCH2, NOTCH1, NOTCH3, MLLT4, MIB1, HGS, NEURL1, FBXW7, APBB1SLX4IPSLX4, PAGR1, RNF20, FBXW4, ERCC4, STK4, SYNE2, COPS7A, CUL1, RPN1, RNH1, SLX1B, PLK1, SUMO2, ERCC1, PDCD2L, DLD, MAPK14, IFI30, GORASP1


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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RelatedDrugs for JAG1_SLX4IP


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for JAG1_SLX4IP


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneJAG1C1956125Alagille Syndrome 113ORPHANET;UNIPROT
HgeneJAG1C0015393Eye Abnormalities3CTD_human
HgeneJAG1C0085280Alagille Syndrome3CTD_human
HgeneJAG1C0039685Tetralogy of Fallot2CTD_human;HPO;ORPHANET;UNIPROT
HgeneJAG1C0282631Facies2CTD_human
HgeneJAG1C0005940Bone Diseases1CTD_human
HgeneJAG1C0010038Corneal Opacity1CTD_human
HgeneJAG1C0010606Adenoid Cystic Carcinoma1CTD_human
HgeneJAG1C0011053Deafness1CTD_human
HgeneJAG1C0017636Glioblastoma1CTD_human
HgeneJAG1C0018798Congenital Heart Defects1CTD_human
HgeneJAG1C0024121Lung Neoplasms1CTD_human
HgeneJAG1C0036095Salivary Gland Neoplasms1CTD_human
HgeneJAG1C0036341Schizophrenia1PSYGENET
HgeneJAG1C0887833Carcinoma, Pancreatic Ductal1CTD_human
HgeneJAG1C1458155Mammary Neoplasms1CTD_human