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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:CHCHD10-NCKAP5 (FusionGDB2 ID:16214)

Fusion Gene Summary for CHCHD10-NCKAP5

check button Fusion gene summary
Fusion gene informationFusion gene name: CHCHD10-NCKAP5
Fusion gene ID: 16214
HgeneTgene
Gene symbol

CHCHD10

NCKAP5

Gene ID

400916

344148

Gene namecoiled-coil-helix-coiled-coil-helix domain containing 10NCK associated protein 5
SynonymsC22orf16|FTDALS2|IMMD|MIX17A|N27C7-4|SMAJERIH1|ERIH2|NAP5
Cytomap

22q11.23

2q21.2

Type of geneprotein-codingprotein-coding
Descriptioncoiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrialMIX17 homolog Anck-associated protein 5NAP-5peripheral clock protein 2
Modification date2020032720200313
UniProtAcc

Q8WYQ3

Q9HCH0

Ensembl transtripts involved in fusion geneENST00000401675, ENST00000484558, 
ENST00000520222, 
ENST00000317721, 
ENST00000405974, ENST00000409213, 
ENST00000409261, ENST00000473859, 
Fusion gene scores* DoF score1 X 1 X 1=114 X 14 X 5=980
# samples 115
** MAII scorelog2(1/1*10)=3.32192809488736log2(15/980*10)=-2.70781924850669
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CHCHD10 [Title/Abstract] AND NCKAP5 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCHCHD10(24108027)-NCKAP5(134030063), # 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

check buttonFusion gene breakpoints across CHCHD10 (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 NCKAP5 (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
ChiTaRS5.0N/AFN163893CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-


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Fusion Gene ORF analysis for CHCHD10-NCKAP5

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-intronENST00000401675ENST00000317721CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000401675ENST00000405974CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000401675ENST00000409213CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000401675ENST00000409261CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000401675ENST00000473859CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000484558ENST00000317721CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000484558ENST00000405974CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000484558ENST00000409213CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000484558ENST00000409261CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000484558ENST00000473859CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000520222ENST00000317721CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000520222ENST00000405974CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000520222ENST00000409213CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000520222ENST00000409261CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-
intron-intronENST00000520222ENST00000473859CHCHD10chr22

24108027

-NCKAP5chr2

134030063

-

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 CHCHD10-NCKAP5


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 CHCHD10-NCKAP5


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/:24108027/:134030063)
- 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
CHCHD10

Q8WYQ3

NCKAP5

Q9HCH0

FUNCTION: May be involved in the maintenance of mitochondrial organization and mitochondrial cristae structure. {ECO:0000269|PubMed:24934289}.FUNCTION: Regulates microtubule organization and stabilization. Promotes microtubule growth and bundling formation and stabilizes microtubules by increasing intense acetylation of microtubules (PubMed:26482847, PubMed:26485573). Both tubulin-binding and homodimer formation are required for NCKAP5L-mediated microtubule bundle formation (PubMed:26485573). {ECO:0000269|PubMed:26482847, ECO:0000269|PubMed:26485573}.

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 CHCHD10-NCKAP5


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 CHCHD10-NCKAP5


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 CHCHD10-NCKAP5


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 CHCHD10-NCKAP5


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