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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:VAC14-HYDIN (FusionGDB2 ID:97174)

Fusion Gene Summary for VAC14-HYDIN

check button Fusion gene summary
Fusion gene informationFusion gene name: VAC14-HYDIN
Fusion gene ID: 97174
HgeneTgene
Gene symbol

VAC14

HYDIN

Gene ID

55697

54768

Gene nameVAC14 component of PIKFYVE complexHYDIN axonemal central pair apparatus protein
SynonymsArPIKfyve|TAX1BP2|TRXCILD5|HYDIN1|HYDIN2|PPP1R31
Cytomap

16q22.1-q22.2

16q22.2

Type of geneprotein-codingprotein-coding
Descriptionprotein VAC14 homologTax1 (human T-cell leukemia virus type I) binding proteinVac14, PIKFYVE complex componenthydrocephalus-inducing protein homologprotein phosphatase 1, regulatory subunit 31
Modification date2020032720200313
UniProtAcc.

Q4G0P3

Ensembl transtripts involved in fusion geneENST00000261776, ENST00000571759, 
ENST00000536184, 
ENST00000393567, 
ENST00000448089, ENST00000448691, 
ENST00000321489, ENST00000538248, 
ENST00000541601, ENST00000288168, 
ENST00000393550, ENST00000543639, 
Fusion gene scores* DoF score5 X 6 X 4=1205 X 5 X 4=100
# samples 67
** MAII scorelog2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/100*10)=-0.514573172829758
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: VAC14 [Title/Abstract] AND HYDIN [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointVAC14(70834700)-HYDIN(70913659), # samples:5
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 VAC14 (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 HYDIN (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
ChimerDB4LUADTCGA-44-5645-01AVAC14chr16

70834700

-HYDINchr16

70913659

-
ChimerDB4LUADTCGA-44-5645-01BVAC14chr16

70834700

-HYDINchr16

70913659

-
ChimerDB4LUADTCGA-44-5645-01AVAC14chr16

70834700

-HYDINchr16

70913659

-
ChimerDB4LUADTCGA-44-5645-01AVAC14chr16

70834700

-HYDINchr16

70913659

-
ChimerDB4LUADTCGA-44-5645-01AVAC14chr16

70834700

-HYDINchr16

70913659

-


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Fusion Gene ORF analysis for VAC14-HYDIN

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
In-frameENST00000261776ENST00000393567VAC14chr16

70834700

-HYDINchr16

70913659

-
5CDS-intronENST00000261776ENST00000448089VAC14chr16

70834700

-HYDINchr16

70913659

-
5CDS-intronENST00000261776ENST00000448691VAC14chr16

70834700

-HYDINchr16

70913659

-
5CDS-intronENST00000261776ENST00000321489VAC14chr16

70834700

-HYDINchr16

70913659

-
5CDS-intronENST00000261776ENST00000538248VAC14chr16

70834700

-HYDINchr16

70913659

-
5CDS-intronENST00000261776ENST00000541601VAC14chr16

70834700

-HYDINchr16

70913659

-
5CDS-intronENST00000261776ENST00000288168VAC14chr16

70834700

-HYDINchr16

70913659

-
5CDS-intronENST00000261776ENST00000393550VAC14chr16

70834700

-HYDINchr16

70913659

-
5CDS-intronENST00000261776ENST00000543639VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-3CDSENST00000571759ENST00000393567VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000571759ENST00000448089VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000571759ENST00000448691VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000571759ENST00000321489VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000571759ENST00000538248VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000571759ENST00000541601VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000571759ENST00000288168VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000571759ENST00000393550VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000571759ENST00000543639VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-3CDSENST00000536184ENST00000393567VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000536184ENST00000448089VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000536184ENST00000448691VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000536184ENST00000321489VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000536184ENST00000538248VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000536184ENST00000541601VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000536184ENST00000288168VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000536184ENST00000393550VAC14chr16

70834700

-HYDINchr16

70913659

-
intron-intronENST00000536184ENST00000543639VAC14chr16

70834700

-HYDINchr16

70913659

-

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 VAC14-HYDIN


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 VAC14-HYDIN


check button Go to

FGviewer for the breakpoints of chr16:70834700-chr16:70913659

.
- 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
.HYDIN

Q4G0P3

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.FUNCTION: Required for ciliary motility. {ECO:0000250}.

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
TgeneHYDINchr16:70834700chr16:70913659ENST000003214890201908_193301018.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000003214890202267_236501018.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000003214890202504_254901018.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000004486910201908_193301018.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000004486910202267_236501018.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000004486910202504_254901018.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000005382480191908_19330951.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000005382480192267_23650951.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000005382480192504_25490951.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000005416010191908_19330941.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000005416010192267_23650941.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000005416010192504_25490941.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST000003214890201975_198101018.0Compositional biasNote=Poly-Glu
TgeneHYDINchr16:70834700chr16:70913659ENST000004486910201975_198101018.0Compositional biasNote=Poly-Glu
TgeneHYDINchr16:70834700chr16:70913659ENST000005382480191975_19810951.0Compositional biasNote=Poly-Glu
TgeneHYDINchr16:70834700chr16:70913659ENST000005416010191975_19810941.0Compositional biasNote=Poly-Glu

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneVAC14chr16:70834700chr16:70913659ENST00000261776-119171_20834.666666666666664783.0RepeatNote=HEAT 3
HgeneVAC14chr16:70834700chr16:70913659ENST00000261776-119212_24934.666666666666664783.0RepeatNote=HEAT 4
HgeneVAC14chr16:70834700chr16:70913659ENST00000261776-119438_47534.666666666666664783.0RepeatNote=HEAT 5
HgeneVAC14chr16:70834700chr16:70913659ENST00000261776-119560_59834.666666666666664783.0RepeatNote=HEAT 6
HgeneVAC14chr16:70834700chr16:70913659ENST00000261776-1195_4234.666666666666664783.0RepeatNote=HEAT 1
HgeneVAC14chr16:70834700chr16:70913659ENST00000261776-11989_12634.666666666666664783.0RepeatNote=HEAT 2
TgeneHYDINchr16:70834700chr16:70913659ENST0000039356759861908_19333405.05122.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST0000039356759862267_23653405.05122.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST0000039356759862504_25493405.05122.0Coiled coilOntology_term=ECO:0000255
TgeneHYDINchr16:70834700chr16:70913659ENST0000039356759861975_19813405.05122.0Compositional biasNote=Poly-Glu


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Fusion Gene Sequence for VAC14-HYDIN


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 VAC14-HYDIN


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 VAC14-HYDIN


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 VAC14-HYDIN


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneVAC14C4310743STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET2CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneVAC14C1857663Yunis Varon syndrome1ORPHANET
TgeneHYDINC0009451Communicating Hydrocephalus2CTD_human
TgeneHYDINC0020255Hydrocephalus2CTD_human
TgeneHYDINC0020256Congenital Hydrocephalus2CTD_human
TgeneHYDINC0270720Hydrocephalus Ex-Vacuo2CTD_human
TgeneHYDINC0477432Post-Traumatic Hydrocephalus2CTD_human
TgeneHYDINC0549423Obstructive Hydrocephalus2CTD_human
TgeneHYDINC1531647Cerebral ventriculomegaly2CTD_human
TgeneHYDINC1837615Ciliary Dyskinesia, Primary, 52CTD_human;GENOMICS_ENGLAND
TgeneHYDINC2936718Fetal Cerebral Ventriculomegaly2CTD_human
TgeneHYDINC2936786Aqueductal Stenosis2CTD_human
TgeneHYDINC0022521Kartagener Syndrome1ORPHANET
TgeneHYDINC4317124Polynesian Bronchiectasis1ORPHANET
TgeneHYDINC4551720Primary Ciliary Dyskinesia1ORPHANET
TgeneHYDINC4551906Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus1ORPHANET