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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: 35641

FusionGeneSummary for SPEG_ZNF622

check button Fusion gene summary
Fusion gene informationFusion gene name: SPEG_ZNF622
Fusion gene ID: 35641
HgeneTgene
Gene symbol

SPEG

ZNF622

Gene ID

10290

90441

Gene nameSPEG complex locuszinc finger protein 622
SynonymsAPEG-1|APEG1|BPEG|CNM5|SPEGalpha|SPEGbetaZPR9
Cytomap

2q35

5p15.1

Type of geneprotein-codingprotein-coding
Descriptionstriated muscle preferentially expressed protein kinaseaortic preferentially expressed gene 1aortic preferentially expressed protein 1nuclear protein, marker for differentiated aortic smooth muscle and down-regulated with vascular injuryzinc finger protein 622zinc finger-like protein 9
Modification date2018052320180523
UniProtAcc

Q15772

Q969S3

Ensembl transtripts involved in fusion geneENST00000312358, ENST00000485813, 
ENST00000396698, ENST00000396695, 
ENST00000396688, ENST00000396686, 
ENST00000396689, 
ENST00000308683, 
Fusion gene scores* DoF score1 X 1 X 1=14 X 4 X 4=64
# samples 14
** MAII scorelog2(1/1*10)=3.32192809488736log2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SPEG [Title/Abstract] AND ZNF622 [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
TgeneZNF622

GO:0008631

intrinsic apoptotic signaling pathway in response to oxidative stress

21771788

TgeneZNF622

GO:0033674

positive regulation of kinase activity

21771788

TgeneZNF622

GO:0043065

positive regulation of apoptotic process

21771788

TgeneZNF622

GO:0043410

positive regulation of MAPK cascade

21771788


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
ChiTaRS3.1Z28494SPEGchr2

220358258

-ZNF622chr5

16465475

-
* 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
3UTR-3CDSENST00000312358ENST00000308683SPEGchr2

220358258

-ZNF622chr5

16465475

-
3UTR-3CDSENST00000485813ENST00000308683SPEGchr2

220358258

-ZNF622chr5

16465475

-
intron-3CDSENST00000396698ENST00000308683SPEGchr2

220358258

-ZNF622chr5

16465475

-
intron-3CDSENST00000396695ENST00000308683SPEGchr2

220358258

-ZNF622chr5

16465475

-
intron-3CDSENST00000396688ENST00000308683SPEGchr2

220358258

-ZNF622chr5

16465475

-
intron-3CDSENST00000396686ENST00000308683SPEGchr2

220358258

-ZNF622chr5

16465475

-
intron-3CDSENST00000396689ENST00000308683SPEGchr2

220358258

-ZNF622chr5

16465475

-

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FusionProtFeatures for SPEG_ZNF622


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

Q15772

ZNF622

Q969S3

May behave as an activator of the bound transcriptionfactor, MYBL2, and be involved in embryonic development.

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 SPEG_ZNF622


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 SPEG_ZNF622


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 SPEG_ZNF622


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 SPEG_ZNF622


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSPEGC4014814MYOPATHY, CENTRONUCLEAR, 51UNIPROT