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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: 24519

FusionGeneSummary for NMUR1_FZR1

check button Fusion gene summary
Fusion gene informationFusion gene name: NMUR1_FZR1
Fusion gene ID: 24519
HgeneTgene
Gene symbol

NMUR1

FZR1

Gene ID

10316

51343

Gene nameneuromedin U receptor 1fizzy and cell division cycle 20 related 1
Synonyms(FM-3)|FM-3|FM3|GPC-R|GPR66|NMU1RCDC20C|CDH1|FZR|FZR2|HCDH|HCDH1
Cytomap

2q37.1

19p13.3

Type of geneprotein-codingprotein-coding
Descriptionneuromedin-U receptor 1G-protein coupled receptor 66G-protein coupled receptor FM-3NMU-R1fizzy-related protein homologCDC20 homolog 1CDC20-like 1bCDC20-like protein 1cdh1/Hct1 homologfizzy/cell division cycle 20 related 1
Modification date2018051920180519
UniProtAcc

Q9HB89

Q9UM11

Ensembl transtripts involved in fusion geneENST00000305141, ENST00000441788, 
ENST00000313639, ENST00000395095, 
Fusion gene scores* DoF score2 X 2 X 2=85 X 4 X 3=60
# samples 25
** MAII scorelog2(2/8*10)=1.32192809488736log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NMUR1 [Title/Abstract] AND FZR1 [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
HgeneNMUR1

GO:0006816

calcium ion transport

10899166

HgeneNMUR1

GO:0006821

chloride transport

10899166

HgeneNMUR1

GO:0007200

phospholipase C-activating G-protein coupled receptor signaling pathway

10899166

HgeneNMUR1

GO:0007202

activation of phospholipase C activity

10899166

HgeneNMUR1

GO:0019722

calcium-mediated signaling

10894543|10899166|11027493

HgeneNMUR1

GO:0048016

inositol phosphate-mediated signaling

10899166

TgeneFZR1

GO:0031145

anaphase-promoting complex-dependent catabolic process

18662541|21596315

TgeneFZR1

GO:0072425

signal transduction involved in G2 DNA damage checkpoint

18662541

TgeneFZR1

GO:1904668

positive regulation of ubiquitin protein ligase activity

11459826


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
ChiTaRS3.1BG989333NMUR1chr2

232391697

-FZR1chr19

3535226

-
* 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-3UTRENST00000305141ENST00000441788NMUR1chr2

232391697

-FZR1chr19

3535226

-
intron-intronENST00000305141ENST00000313639NMUR1chr2

232391697

-FZR1chr19

3535226

-
intron-intronENST00000305141ENST00000395095NMUR1chr2

232391697

-FZR1chr19

3535226

-

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FusionProtFeatures for NMUR1_FZR1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NMUR1

Q9HB89

FZR1

Q9UM11

Receptor for the neuromedin-U and neuromedin-Sneuropeptides. {ECO:0000250, ECO:0000269|PubMed:10899166}.

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 NMUR1_FZR1


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 NMUR1_FZR1


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 NMUR1_FZR1


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 NMUR1_FZR1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneFZR1C0032578Polyploidy1CTD_human