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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:KANSL2-DDX23 (FusionGDB2 ID:41157)

Fusion Gene Summary for KANSL2-DDX23

check button Fusion gene summary
Fusion gene informationFusion gene name: KANSL2-DDX23
Fusion gene ID: 41157
HgeneTgene
Gene symbol

KANSL2

DDX23

Gene ID

54934

9416

Gene nameKAT8 regulatory NSL complex subunit 2DEAD-box helicase 23
SynonymsC12orf41|NSL2PRPF28|SNRNP100|U5-100K|U5-100KD|prp28
Cytomap

12q13.11

12q13.12

Type of geneprotein-codingprotein-coding
DescriptionKAT8 regulatory NSL complex subunit 2NSL complex protein NSL2non-specific lethal 2 homologprobable ATP-dependent RNA helicase DDX23100 kDa U5 snRNP-specific proteinDEAD (Asp-Glu-Ala-Asp) box polypeptide 23DEAD box protein 23PRP28 homolog, yeastPRP28p homologU5 snRNP 100 kD protein
Modification date2020031320200313
UniProtAcc

Q9H9L4

Q9BUQ8

Ensembl transtripts involved in fusion geneENST00000357861, ENST00000420613, 
ENST00000548701, ENST00000550347, 
ENST00000553086, 
ENST00000308025, 
ENST00000553182, 
Fusion gene scores* DoF score4 X 4 X 4=646 X 6 X 4=144
# samples 47
** MAII scorelog2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/144*10)=-1.04064198449735
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KANSL2 [Title/Abstract] AND DDX23 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointKANSL2(49061547)-DDX23(49224475), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneKANSL2

GO:0043981

histone H4-K5 acetylation

20018852

HgeneKANSL2

GO:0043982

histone H4-K8 acetylation

20018852

HgeneKANSL2

GO:0043984

histone H4-K16 acetylation

20018852


check buttonFusion gene breakpoints across KANSL2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across DDX23 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4ESCATCGA-2H-A9GNKANSL2chr12

49061547

-DDX23chr12

49224475

-


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Fusion Gene ORF analysis for KANSL2-DDX23

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
intron-3CDSENST00000357861ENST00000308025KANSL2chr12

49061547

-DDX23chr12

49224475

-
intron-3CDSENST00000420613ENST00000308025KANSL2chr12

49061547

-DDX23chr12

49224475

-
intron-3CDSENST00000548701ENST00000308025KANSL2chr12

49061547

-DDX23chr12

49224475

-
intron-3CDSENST00000550347ENST00000308025KANSL2chr12

49061547

-DDX23chr12

49224475

-
intron-3CDSENST00000553086ENST00000308025KANSL2chr12

49061547

-DDX23chr12

49224475

-
intron-intronENST00000357861ENST00000553182KANSL2chr12

49061547

-DDX23chr12

49224475

-
intron-intronENST00000420613ENST00000553182KANSL2chr12

49061547

-DDX23chr12

49224475

-
intron-intronENST00000548701ENST00000553182KANSL2chr12

49061547

-DDX23chr12

49224475

-
intron-intronENST00000550347ENST00000553182KANSL2chr12

49061547

-DDX23chr12

49224475

-
intron-intronENST00000553086ENST00000553182KANSL2chr12

49061547

-DDX23chr12

49224475

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

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

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Fusion Genomic Features for KANSL2-DDX23


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for KANSL2-DDX23


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/:49061547/:49224475)
- 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
KANSL2

Q9H9L4

DDX23

Q9BUQ8

FUNCTION: As part of the NSL complex it is involved in acetylation of nucleosomal histone H4 on several lysine residues and therefore may be involved in the regulation of transcription. {ECO:0000269|PubMed:20018852}.FUNCTION: Involved in pre-mRNA splicing and its phosphorylated form (by SRPK2) is required for spliceosomal B complex formation (PubMed:18425142). Independently of its spliceosome formation function, required for the suppression of incorrect R-loops formed during transcription; R-loops are composed of a DNA:RNA hybrid and the associated non-template single-stranded DNA (PubMed:28076779). {ECO:0000269|PubMed:18425142, ECO:0000269|PubMed:28076779}.

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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Fusion Gene Sequence for KANSL2-DDX23


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for KANSL2-DDX23


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


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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Related Drugs for KANSL2-DDX23


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for KANSL2-DDX23


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