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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:KIF13A-OVOL2 (FusionGDB2 ID:42343)

Fusion Gene Summary for KIF13A-OVOL2

check button Fusion gene summary
Fusion gene informationFusion gene name: KIF13A-OVOL2
Fusion gene ID: 42343
HgeneTgene
Gene symbol

KIF13A

OVOL2

Gene ID

63971

58495

Gene namekinesin family member 13Aovo like zinc finger 2
SynonymsRBKIN|bA500C11.2CHED|CHED1|CHED2|EUROIMAGE566589|PPCD1|ZNF339
Cytomap

6p22.3

20p11.23

Type of geneprotein-codingprotein-coding
Descriptionkinesin-like protein KIF13Ahomolog of mouse KIF13A mannose-6-phosphate receptor transporterkinesin-like protein RBKINtranscription factor Ovo-like 2corneal endothelial dystrophy 1 (autosomal dominant)zinc finger protein 339
Modification date2020031320200320
UniProtAcc

Q9H1H9

.
Ensembl transtripts involved in fusion geneENST00000378814, ENST00000259711, 
ENST00000378843, ENST00000378826, 
ENST00000378816, ENST00000502704, 
ENST00000503342, 
ENST00000278780, 
ENST00000483661, 
Fusion gene scores* DoF score14 X 12 X 9=15127 X 5 X 4=140
# samples 177
** MAII scorelog2(17/1512*10)=-3.15285148808337
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/140*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KIF13A [Title/Abstract] AND OVOL2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointKIF13A(17817250)-OVOL2(18005596), # samples:1
Anticipated loss of major functional domain due to fusion event.KIF13A-OVOL2 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
KIF13A-OVOL2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
KIF13A-OVOL2 seems lost the major protein functional domain in Tgene partner, which is a transcription factor 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 KIF13A (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 OVOL2 (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-BR-7958KIF13Achr6

17817250

-OVOL2chr20

18005596

-


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Fusion Gene ORF analysis for KIF13A-OVOL2

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
Frame-shiftENST00000378814ENST00000278780KIF13Achr6

17817250

-OVOL2chr20

18005596

-
5CDS-5UTRENST00000378814ENST00000483661KIF13Achr6

17817250

-OVOL2chr20

18005596

-
Frame-shiftENST00000259711ENST00000278780KIF13Achr6

17817250

-OVOL2chr20

18005596

-
5CDS-5UTRENST00000259711ENST00000483661KIF13Achr6

17817250

-OVOL2chr20

18005596

-
Frame-shiftENST00000378843ENST00000278780KIF13Achr6

17817250

-OVOL2chr20

18005596

-
5CDS-5UTRENST00000378843ENST00000483661KIF13Achr6

17817250

-OVOL2chr20

18005596

-
Frame-shiftENST00000378826ENST00000278780KIF13Achr6

17817250

-OVOL2chr20

18005596

-
5CDS-5UTRENST00000378826ENST00000483661KIF13Achr6

17817250

-OVOL2chr20

18005596

-
Frame-shiftENST00000378816ENST00000278780KIF13Achr6

17817250

-OVOL2chr20

18005596

-
5CDS-5UTRENST00000378816ENST00000483661KIF13Achr6

17817250

-OVOL2chr20

18005596

-
intron-3CDSENST00000502704ENST00000278780KIF13Achr6

17817250

-OVOL2chr20

18005596

-
intron-5UTRENST00000502704ENST00000483661KIF13Achr6

17817250

-OVOL2chr20

18005596

-
5UTR-3CDSENST00000503342ENST00000278780KIF13Achr6

17817250

-OVOL2chr20

18005596

-
5UTR-5UTRENST00000503342ENST00000483661KIF13Achr6

17817250

-OVOL2chr20

18005596

-

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 KIF13A-OVOL2


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 KIF13A-OVOL2


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
KIF13A

Q9H1H9

.
FUNCTION: Plus end-directed microtubule-dependent motor protein involved in intracellular transport and regulating various processes such as mannose-6-phosphate receptor (M6PR) transport to the plasma membrane, endosomal sorting during melanosome biogenesis and cytokinesis. Mediates the transport of M6PR-containing vesicles from trans-Golgi network to the plasma membrane via direct interaction with the AP-1 complex. During melanosome maturation, required for delivering melanogenic enzymes from recycling endosomes to nascent melanosomes by creating peripheral recycling endosomal subdomains in melanocytes. Also required for the abcission step in cytokinesis: mediates translocation of ZFYVE26, and possibly TTC19, to the midbody during cytokinesis. {ECO:0000269|PubMed:19841138, ECO:0000269|PubMed:20208530}.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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 KIF13A-OVOL2


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 KIF13A-OVOL2


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 KIF13A-OVOL2


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 KIF13A-OVOL2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneOVOL2C0206711Pilomatrixoma1CTD_human
TgeneOVOL2C0339284Polymorphous corneal dystrophy1ORPHANET
TgeneOVOL2C1562689Congenital hereditary endothelial dystrophy1ORPHANET
TgeneOVOL2C1852555CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT1CTD_human;GENOMICS_ENGLAND