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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:CAND2-IFT122 (FusionGDB2 ID:12777)

Fusion Gene Summary for CAND2-IFT122

check button Fusion gene summary
Fusion gene informationFusion gene name: CAND2-IFT122
Fusion gene ID: 12777
HgeneTgene
Gene symbol

CAND2

IFT122

Gene ID

23066

55764

Gene namecullin associated and neddylation dissociated 2 (putative)intraflagellar transport 122
SynonymsTIP120B|Tp120bCED|CED1|FAP80|SPG|WDR10|WDR10p|WDR140
Cytomap

3p25.2

3q21.3-q22.1

Type of geneprotein-codingprotein-coding
Descriptioncullin-associated NEDD8-dissociated protein 2TBP interacting proteinTBP-interacting protein 120BTBP-interacting protein of 120 kDa Bcullin-associated and neddylation-dissociated protein 2epididymis secretory sperm binding proteinepididymis tissue printraflagellar transport protein 122 homologWD repeat domain 10WD repeat-containing protein 10WD repeat-containing protein 140intraflagellar transport 122 homolog
Modification date2020031320200313
UniProtAcc

O75155

Q9HBG6

Ensembl transtripts involved in fusion geneENST00000295989, ENST00000456430, 
ENST00000466558, 
ENST00000513932, 
ENST00000296266, ENST00000347300, 
ENST00000348417, ENST00000349441, 
ENST00000431818, ENST00000440957, 
ENST00000504021, ENST00000507564, 
Fusion gene scores* DoF score2 X 2 X 2=87 X 8 X 4=224
# samples 28
** MAII scorelog2(2/8*10)=1.32192809488736log2(8/224*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CAND2 [Title/Abstract] AND IFT122 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCAND2(12845130)-IFT122(129202327), # samples:1
Anticipated loss of major functional domain due to fusion event.CAND2-IFT122 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CAND2-IFT122 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* 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 CAND2 (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 IFT122 (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
ChimerDB4OVTCGA-36-1577CAND2chr3

12845130

+IFT122chr3

129202327

+


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Fusion Gene ORF analysis for CAND2-IFT122

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-intronENST00000295989ENST00000513932CAND2chr3

12845130

+IFT122chr3

129202327

+
5CDS-intronENST00000456430ENST00000513932CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000295989ENST00000296266CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000295989ENST00000347300CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000295989ENST00000348417CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000295989ENST00000349441CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000295989ENST00000431818CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000295989ENST00000440957CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000295989ENST00000504021CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000295989ENST00000507564CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000456430ENST00000296266CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000456430ENST00000347300CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000456430ENST00000348417CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000456430ENST00000349441CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000456430ENST00000431818CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000456430ENST00000440957CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000456430ENST00000504021CAND2chr3

12845130

+IFT122chr3

129202327

+
Frame-shiftENST00000456430ENST00000507564CAND2chr3

12845130

+IFT122chr3

129202327

+
intron-3CDSENST00000466558ENST00000296266CAND2chr3

12845130

+IFT122chr3

129202327

+
intron-3CDSENST00000466558ENST00000347300CAND2chr3

12845130

+IFT122chr3

129202327

+
intron-3CDSENST00000466558ENST00000348417CAND2chr3

12845130

+IFT122chr3

129202327

+
intron-3CDSENST00000466558ENST00000349441CAND2chr3

12845130

+IFT122chr3

129202327

+
intron-3CDSENST00000466558ENST00000431818CAND2chr3

12845130

+IFT122chr3

129202327

+
intron-3CDSENST00000466558ENST00000440957CAND2chr3

12845130

+IFT122chr3

129202327

+
intron-3CDSENST00000466558ENST00000504021CAND2chr3

12845130

+IFT122chr3

129202327

+
intron-3CDSENST00000466558ENST00000507564CAND2chr3

12845130

+IFT122chr3

129202327

+
intron-intronENST00000466558ENST00000513932CAND2chr3

12845130

+IFT122chr3

129202327

+

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 CAND2-IFT122


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)
CAND2chr312845130+IFT122chr3129202327+4.81E-101
CAND2chr312845130+IFT122chr3129202327+4.81E-101

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.
genomic feature of top 1%

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Fusion Protein Features for CAND2-IFT122


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/:12845130/:129202327)
- 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
CAND2

O75155

IFT122

Q9HBG6

FUNCTION: Probable assembly factor of SCF (SKP1-CUL1-F-box protein) E3 ubiquitin ligase complexes that promotes the exchange of the substrate-recognition F-box subunit in SCF complexes, thereby playing a key role in the cellular repertoire of SCF complexes. {ECO:0000250}.FUNCTION: As a component of the IFT complex A (IFT-A), a complex required for retrograde ciliary transport and entry into cilia of G protein-coupled receptors (GPCRs), it is required in ciliogenesis and ciliary protein trafficking (PubMed:27932497, PubMed:29220510). Involved in cilia formation during neuronal patterning. Acts as a negative regulator of Shh signaling. Required to recruit TULP3 to primary cilia (By similarity). {ECO:0000250|UniProtKB:Q6NWV3, ECO:0000269|PubMed:27932497, ECO:0000269|PubMed:29220510}.

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 CAND2-IFT122


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 CAND2-IFT122


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 CAND2-IFT122


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 CAND2-IFT122


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