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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: 13606

FusionGeneSummary for FMN1_UBALD2

check button Fusion gene summary
Fusion gene informationFusion gene name: FMN1_UBALD2
Fusion gene ID: 13606
HgeneTgene
Gene symbol

FMN1

UBALD2

Gene ID

342184

283991

Gene nameformin 1UBA like domain containing 2
SynonymsFMN|LDFAM100B
Cytomap

15q13.3

17q25.1

Type of geneprotein-codingprotein-coding
Descriptionformin-1formin (limb deformity)limb deformity protein homologUBA-like domain-containing protein 2family with sequence similarity 100, member Bprotein FAM100B
Modification date2018051920180329
UniProtAcc

Q68DA7

Q8IYN6

Ensembl transtripts involved in fusion geneENST00000334528, ENST00000561249, 
ENST00000559047, ENST00000558197, 
ENST00000559150, ENST00000320930, 
ENST00000327490, ENST00000589240, 
Fusion gene scores* DoF score9 X 6 X 5=2701 X 1 X 1=1
# samples 91
** MAII scorelog2(9/270*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: FMN1 [Title/Abstract] AND UBALD2 [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
TCGALDSKCMTCGA-WE-A8ZT-06AFMN1chr15

33218375

-UBALD2chr17

74266275

+
* 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
Frame-shiftENST00000334528ENST00000327490FMN1chr15

33218375

-UBALD2chr17

74266275

+
Frame-shiftENST00000334528ENST00000589240FMN1chr15

33218375

-UBALD2chr17

74266275

+
Frame-shiftENST00000561249ENST00000327490FMN1chr15

33218375

-UBALD2chr17

74266275

+
Frame-shiftENST00000561249ENST00000589240FMN1chr15

33218375

-UBALD2chr17

74266275

+
Frame-shiftENST00000559047ENST00000327490FMN1chr15

33218375

-UBALD2chr17

74266275

+
Frame-shiftENST00000559047ENST00000589240FMN1chr15

33218375

-UBALD2chr17

74266275

+
intron-3CDSENST00000558197ENST00000327490FMN1chr15

33218375

-UBALD2chr17

74266275

+
intron-3CDSENST00000558197ENST00000589240FMN1chr15

33218375

-UBALD2chr17

74266275

+
intron-3CDSENST00000559150ENST00000327490FMN1chr15

33218375

-UBALD2chr17

74266275

+
intron-3CDSENST00000559150ENST00000589240FMN1chr15

33218375

-UBALD2chr17

74266275

+
intron-3CDSENST00000320930ENST00000327490FMN1chr15

33218375

-UBALD2chr17

74266275

+
intron-3CDSENST00000320930ENST00000589240FMN1chr15

33218375

-UBALD2chr17

74266275

+

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FusionProtFeatures for FMN1_UBALD2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FMN1

Q68DA7

UBALD2

Q8IYN6

Plays a role in the formation of adherens junction andthe polymerization of linear actin cables. {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 FMN1_UBALD2


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 FMN1_UBALD2


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
FMN1PRPF40A, NUP85, LLGL2, CDH1, CYP2S1, NAPGUBALD2


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 FMN1_UBALD2


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 FMN1_UBALD2


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