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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: 43478

FusionGeneSummary for ZNF587B_TMEM150B

check button Fusion gene summary
Fusion gene informationFusion gene name: ZNF587B_TMEM150B
Fusion gene ID: 43478
HgeneTgene
Gene symbol

ZNF587B

TMEM150B

Gene ID

100293516

284417

Gene namezinc finger protein 587Btransmembrane protein 150B
Synonyms-DRAM3|TMEM224|TTN2
Cytomap

19q13.43

19q13.42

Type of geneprotein-codingprotein-coding
Descriptionzinc finger protein 587Bmodulator of macroautophagy TMEM150BhCG1651476protein DRAM-3tentonin 2transmembrane protein 224transmembrane protein LOC284417
Modification date2018052320180523
UniProtAcc

E7ETH6

A6NC51

Ensembl transtripts involved in fusion geneENST00000316462, ENST00000442832, 
ENST00000594901, 
ENST00000438693, 
ENST00000326652, 
Fusion gene scores* DoF score4 X 2 X 3=241 X 1 X 1=1
# samples 61
** MAII scorelog2(6/24*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: ZNF587B [Title/Abstract] AND TMEM150B [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
TCGALDBRCATCGA-E9-A1NA-01AZNF587Bchr19

58331313

+TMEM150Bchr19

55834111

-
* 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
5CDS-5UTRENST00000316462ENST00000438693ZNF587Bchr19

58331313

+TMEM150Bchr19

55834111

-
5CDS-5UTRENST00000316462ENST00000326652ZNF587Bchr19

58331313

+TMEM150Bchr19

55834111

-
intron-5UTRENST00000442832ENST00000438693ZNF587Bchr19

58331313

+TMEM150Bchr19

55834111

-
intron-5UTRENST00000442832ENST00000326652ZNF587Bchr19

58331313

+TMEM150Bchr19

55834111

-
intron-5UTRENST00000594901ENST00000438693ZNF587Bchr19

58331313

+TMEM150Bchr19

55834111

-
intron-5UTRENST00000594901ENST00000326652ZNF587Bchr19

58331313

+TMEM150Bchr19

55834111

-

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FusionProtFeatures for ZNF587B_TMEM150B


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ZNF587B

E7ETH6

TMEM150B

A6NC51

May be involved in transcriptional regulation.{ECO:0000305}. Modulator of macroautophagy that causes accumulation ofautophagosomes under basal conditions and enhances autophagic flux(PubMed:25929859). Represses cell death and promotes long-termclonogenic survival of cells grown in the absence of glucose in amacroautophagy-independent manner (PubMed:25929859). May have somerole in extracellular matrix engulfment or growth factor receptorrecycling, both of which can modulate cell survival(PubMed:25929859). {ECO:0000269|PubMed:25929859}.

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 ZNF587B_TMEM150B


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 ZNF587B_TMEM150B


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
ZNF587BSMAD9, TRIM25TMEM150B


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 ZNF587B_TMEM150B


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 ZNF587B_TMEM150B


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