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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: 18463

FusionGeneSummary for KDM4B_SNTG1

check button Fusion gene summary
Fusion gene informationFusion gene name: KDM4B_SNTG1
Fusion gene ID: 18463
HgeneTgene
Gene symbol

KDM4B

SNTG1

Gene ID

23030

54212

Gene namelysine demethylase 4Bsyntrophin gamma 1
SynonymsJMJD2B|TDRD14BG1SYN|SYN4
Cytomap

19p13.3

8q11.21

Type of geneprotein-codingprotein-coding
Descriptionlysine-specific demethylase 4BjmjC domain-containing histone demethylation protein 3Bjumonji domain containing 2Bjumonji domain-containing protein 2Blysine (K)-specific demethylase 4Btudor domain containing 14Bgamma-1-syntrophingamma1-syntrophinsyntrophin 4
Modification date2018052320180519
UniProtAcc

O94953

Q9NSN8

Ensembl transtripts involved in fusion geneENST00000159111, ENST00000381759, 
ENST00000536461, ENST00000592175, 
ENST00000518864, ENST00000522124, 
ENST00000517473, ENST00000276467, 
ENST00000520697, 
Fusion gene scores* DoF score19 X 9 X 12=20526 X 5 X 4=120
# samples 196
** MAII scorelog2(19/2052*10)=-3.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KDM4B [Title/Abstract] AND SNTG1 [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
HgeneKDM4B

GO:0033169

histone H3-K9 demethylation

21914792

HgeneKDM4B

GO:0070544

histone H3-K36 demethylation

21914792


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
TCGALDGBMTCGA-06-2570-01AKDM4Bchr19

5047680

+SNTG1chr8

51085121

+
* 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
5CDS-5UTRENST00000159111ENST00000518864KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-5UTRENST00000159111ENST00000522124KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-intronENST00000159111ENST00000517473KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-intronENST00000159111ENST00000276467KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-intronENST00000159111ENST00000520697KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-5UTRENST00000381759ENST00000518864KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-5UTRENST00000381759ENST00000522124KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-intronENST00000381759ENST00000517473KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-intronENST00000381759ENST00000276467KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-intronENST00000381759ENST00000520697KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-5UTRENST00000536461ENST00000518864KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-5UTRENST00000536461ENST00000522124KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-intronENST00000536461ENST00000517473KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-intronENST00000536461ENST00000276467KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
5CDS-intronENST00000536461ENST00000520697KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
3UTR-5UTRENST00000592175ENST00000518864KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
3UTR-5UTRENST00000592175ENST00000522124KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
3UTR-intronENST00000592175ENST00000517473KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
3UTR-intronENST00000592175ENST00000276467KDM4Bchr19

5047680

+SNTG1chr8

51085121

+
3UTR-intronENST00000592175ENST00000520697KDM4Bchr19

5047680

+SNTG1chr8

51085121

+

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FusionProtFeatures for KDM4B_SNTG1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
KDM4B

O94953

SNTG1

Q9NSN8

Histone demethylase that specifically demethylates 'Lys-9' of histone H3, thereby playing a role in histone code. Does notdemethylate histone H3 'Lys-4', H3 'Lys-27', H3 'Lys-36' nor H4'Lys-20'. Only able to demethylate trimethylated H3 'Lys-9', witha weaker activity than KDM4A, KDM4C and KDM4D. Demethylation ofLys residue generates formaldehyde and succinate.{ECO:0000269|PubMed:16603238, ECO:0000269|PubMed:28262558}. Adapter protein that binds to and probably organizes thesubcellular localization of a variety of proteins. May linkvarious receptors to the actin cytoskeleton and the dystrophinglycoprotein complex (By similarity). May participate inregulating the subcellular location of diacylglycerol kinase-zetato ensure that diacylglycerol is rapidly inactivated followingreceptor activation. {ECO:0000250}.

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 KDM4B_SNTG1


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 KDM4B_SNTG1


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
KDM4BKMT2D, ASH2L, RBBP5, WDR5, HNRNPU, HSPA4, ESR1, KMT2C, SMU1, HSP90AA2P, HSP90B1, H3F3C, ZNF414, DDX3X, NHP2L1, HIST1H2BG, CHORDC1, KDM4A, CCT3, CCT4, CCT6B, CCT2, CCT7, CCDC85C, CCT5, TCP1, CCT6A, CCT8, TRIM25, UHRF2SNTG1SNAP23, STXBP3, VPS45, UBC


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 KDM4B_SNTG1


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 KDM4B_SNTG1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneKDM4BC0025149Medulloblastoma1CTD_human