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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:CIT-CCDC14 (FusionGDB2 ID:16856)

Fusion Gene Summary for CIT-CCDC14

check button Fusion gene summary
Fusion gene informationFusion gene name: CIT-CCDC14
Fusion gene ID: 16856
HgeneTgene
Gene symbol

CIT

CCDC14

Gene ID

79947

64770

Gene namedehydrodolichyl diphosphate synthase subunitcoiled-coil domain containing 14
SynonymsCIT|CPT|DEDSM|DS|HDS|RP59|hCIT-
Cytomap

1p36.11

3q21.1

Type of geneprotein-codingprotein-coding
Descriptiondehydrodolichyl diphosphate synthase complex subunit DHDDScis-IPTasecis-isoprenyltransferasecis-prenyl transferasecis-prenyltransferase subunit hCITdedol-PP synthasedehydrodolichyl diphosphate syntase complex subunit DHDDSepididymis tissue protein coiled-coil domain-containing protein 14
Modification date2020031320200313
UniProtAcc

O14578

Q6ZUS6

Ensembl transtripts involved in fusion geneENST00000261833, ENST00000392521, 
ENST00000537607, 
ENST00000433542, 
ENST00000485727, ENST00000489746, 
ENST00000310351, ENST00000483247, 
ENST00000488653, 
Fusion gene scores* DoF score9 X 9 X 6=48612 X 8 X 7=672
# samples 913
** MAII scorelog2(9/486*10)=-2.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/672*10)=-2.36994960975031
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CIT [Title/Abstract] AND CCDC14 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCIT(120287978)-CCDC14(123675642), # 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
HgeneCIT

GO:0006489

dolichyl diphosphate biosynthetic process

28842490


check buttonFusion gene breakpoints across CIT (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 CCDC14 (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
ChimerDB4STADTCGA-EQ-A4SO-01ACITchr12

120287978

-CCDC14chr3

123675642

-


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Fusion Gene ORF analysis for CIT-CCDC14

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-5UTRENST00000261833ENST00000433542CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-5UTRENST00000261833ENST00000485727CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-5UTRENST00000261833ENST00000489746CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-5UTRENST00000392521ENST00000433542CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-5UTRENST00000392521ENST00000485727CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-5UTRENST00000392521ENST00000489746CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-intronENST00000261833ENST00000310351CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-intronENST00000261833ENST00000483247CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-intronENST00000261833ENST00000488653CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-intronENST00000392521ENST00000310351CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-intronENST00000392521ENST00000483247CITchr12

120287978

-CCDC14chr3

123675642

-
5CDS-intronENST00000392521ENST00000488653CITchr12

120287978

-CCDC14chr3

123675642

-
intron-5UTRENST00000537607ENST00000433542CITchr12

120287978

-CCDC14chr3

123675642

-
intron-5UTRENST00000537607ENST00000485727CITchr12

120287978

-CCDC14chr3

123675642

-
intron-5UTRENST00000537607ENST00000489746CITchr12

120287978

-CCDC14chr3

123675642

-
intron-intronENST00000537607ENST00000310351CITchr12

120287978

-CCDC14chr3

123675642

-
intron-intronENST00000537607ENST00000483247CITchr12

120287978

-CCDC14chr3

123675642

-
intron-intronENST00000537607ENST00000488653CITchr12

120287978

-CCDC14chr3

123675642

-

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 CIT-CCDC14


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 CIT-CCDC14


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/:120287978/:123675642)
- 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
CIT

O14578

CCDC14

Q6ZUS6

FUNCTION: Plays a role in cytokinesis. Required for KIF14 localization to the central spindle and midbody. Putative RHO/RAC effector that binds to the GTP-bound forms of RHO and RAC1. It probably binds p21 with a tighter specificity in vivo. Displays serine/threonine protein kinase activity. Plays an important role in the regulation of cytokinesis and the development of the central nervous system. Phosphorylates MYL9/MLC2. {ECO:0000269|PubMed:16236794, ECO:0000269|PubMed:16431929, ECO:0000269|PubMed:21457715, ECO:0000269|PubMed:27453578}.

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 CIT-CCDC14


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 CIT-CCDC14


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 CIT-CCDC14


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 CIT-CCDC14


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