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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 16665

FusionGeneSummary for HOMEZ_FBXO34

check button Fusion gene summary
Fusion gene informationFusion gene name: HOMEZ_FBXO34
Fusion gene ID: 16665
HgeneTgene
Gene symbol

HOMEZ

FBXO34

Gene ID

57594

55030

Gene namehomeobox and leucine zipper encodingF-box protein 34
SynonymsKIAA1443CGI-301|Fbx34
Cytomap

14q11.2

14q22.3

Type of geneprotein-codingprotein-coding
Descriptionhomeobox and leucine zipper protein Homezhomeodomain leucine zipper-containing factorF-box only protein 34protein CGI-301
Modification date2018052320180519
UniProtAcc

Q8IX15

Q9NWN3

Ensembl transtripts involved in fusion geneENST00000357460, ENST00000561013, 
ENST00000431326, ENST00000558278, 
ENST00000313833, ENST00000555087, 
ENST00000440021, 
Fusion gene scores* DoF score1 X 1 X 1=15 X 5 X 2=50
# samples 15
** MAII scorelog2(1/1*10)=3.32192809488736log2(5/50*10)=0
Context

PubMed: HOMEZ [Title/Abstract] AND FBXO34 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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 button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1DA330803HOMEZchr14

23768609

-FBXO34chr14

55817097

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-5UTRENST00000357460ENST00000313833HOMEZchr14

23768609

-FBXO34chr14

55817097

+
intron-3UTRENST00000357460ENST00000555087HOMEZchr14

23768609

-FBXO34chr14

55817097

+
intron-5UTRENST00000357460ENST00000440021HOMEZchr14

23768609

-FBXO34chr14

55817097

+
5UTR-5UTRENST00000561013ENST00000313833HOMEZchr14

23768609

-FBXO34chr14

55817097

+
5UTR-3UTRENST00000561013ENST00000555087HOMEZchr14

23768609

-FBXO34chr14

55817097

+
5UTR-5UTRENST00000561013ENST00000440021HOMEZchr14

23768609

-FBXO34chr14

55817097

+
intron-5UTRENST00000431326ENST00000313833HOMEZchr14

23768609

-FBXO34chr14

55817097

+
intron-3UTRENST00000431326ENST00000555087HOMEZchr14

23768609

-FBXO34chr14

55817097

+
intron-5UTRENST00000431326ENST00000440021HOMEZchr14

23768609

-FBXO34chr14

55817097

+
intron-5UTRENST00000558278ENST00000313833HOMEZchr14

23768609

-FBXO34chr14

55817097

+
intron-3UTRENST00000558278ENST00000555087HOMEZchr14

23768609

-FBXO34chr14

55817097

+
intron-5UTRENST00000558278ENST00000440021HOMEZchr14

23768609

-FBXO34chr14

55817097

+

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FusionProtFeatures for HOMEZ_FBXO34


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

Q8IX15

FBXO34

Q9NWN3

May function as a transcriptional regulator. Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex. {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

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for HOMEZ_FBXO34


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for HOMEZ_FBXO34


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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RelatedDrugs for HOMEZ_FBXO34


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for HOMEZ_FBXO34


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