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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: 36289

FusionGeneSummary for ST8SIA2_IGKJ3

check button Fusion gene summary
Fusion gene informationFusion gene name: ST8SIA2_IGKJ3
Fusion gene ID: 36289
HgeneTgene
Gene symbol

ST8SIA2

IGKJ3

Gene ID

8128

28948

Gene nameST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2immunoglobulin kappa joining 3
SynonymsHsT19690|SIAT8-B|SIAT8B|ST8SIA-II|ST8SiaII|STXJ3
Cytomap

15q26.1

2p11.2

Type of geneprotein-codingother
Descriptionalpha-2,8-sialyltransferase 8BST8 alpha-N-acetylneuraminate alpha-2,8-sialyltransferase 2alpha-2,8-sialyltransferase 8B 1sialyltransferase 8 (alpha-2, 8-sialytransferase) Bsialyltransferase 8Bsialyltransferase St8Sia IIsialyltransferase X-
Modification date2018042920180329
UniProtAcc

Q92186

Ensembl transtripts involved in fusion geneENST00000268164, ENST00000539113, 
ENST00000390240, 
Fusion gene scores* DoF score2 X 2 X 2=85 X 4 X 5=100
# samples 25
** MAII scorelog2(2/8*10)=1.32192809488736log2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ST8SIA2 [Title/Abstract] AND IGKJ3 [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
HgeneST8SIA2

GO:0001574

ganglioside biosynthetic process

10766765

HgeneST8SIA2

GO:0006486

protein glycosylation

10766765

HgeneST8SIA2

GO:0006491

N-glycan processing

10766765

HgeneST8SIA2

GO:0009311

oligosaccharide metabolic process

10766765


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
TCGALDLAMLTCGA-AB-2891-03AST8SIA2chr15

93007955

+IGKJ3chr2

89160767

-
* 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
3UTR-3CDSENST00000268164ENST00000390240ST8SIA2chr15

93007955

+IGKJ3chr2

89160767

-
intron-3CDSENST00000539113ENST00000390240ST8SIA2chr15

93007955

+IGKJ3chr2

89160767

-

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FusionProtFeatures for ST8SIA2_IGKJ3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ST8SIA2

Q92186

IGKJ3

May transfer sialic acid through alpha-2,8-linkages tothe alpha-2,3-linked and alpha-2,6-linked sialic acid of N-linkedoligosaccharides of glycoproteins and may be involved in PSA(polysialic acid) expression. Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}.

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 ST8SIA2_IGKJ3


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 ST8SIA2_IGKJ3


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
ST8SIA2IGKJ3


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 ST8SIA2_IGKJ3


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 ST8SIA2_IGKJ3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneST8SIA2C0036341Schizophrenia5PSYGENET
HgeneST8SIA2C0005586Bipolar Disorder2PSYGENET
HgeneST8SIA2C0004352Autistic Disorder1CTD_human