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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: 43655

FusionGeneSummary for ZNF71_HSPB8

check button Fusion gene summary
Fusion gene informationFusion gene name: ZNF71_HSPB8
Fusion gene ID: 43655
HgeneTgene
Gene symbol

ZNF71

HSPB8

Gene ID

58491

26353

Gene namezinc finger protein 71heat shock protein family B (small) member 8
SynonymsEZFITCMT2L|DHMN2|E2IG1|H11|HMN2|HMN2A|HSP22
Cytomap

19q13.43

12q24.23

Type of geneprotein-codingprotein-coding
Descriptionendothelial zinc finger protein induced by tumor necrosis factor alphaKruppel-related zinc finger proteinheat shock protein beta-8E2-induced gene 1 proteinalpha-crystallin C chainheat shock 22kDa protein 8heat shock 27kDa protein 8protein kinase H11small stress protein-like protein HSP22
Modification date2018052320180519
UniProtAcc

Q9NQZ8

Q9UJY1

Ensembl transtripts involved in fusion geneENST00000328070, ENST00000594944, 
ENST00000281938, ENST00000542496, 
Fusion gene scores* DoF score3 X 1 X 1=35 X 3 X 4=60
# samples 25
** MAII scorelog2(2/3*10)=2.73696559416621log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZNF71 [Title/Abstract] AND HSPB8 [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
TCGARVSARCTCGA-DX-A3LS-01AZNF71chr19

57112959

+HSPB8chr12

119624830

+
* 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
5UTR-3CDSENST00000328070ENST00000281938ZNF71chr19

57112959

+HSPB8chr12

119624830

+
5UTR-3UTRENST00000328070ENST00000542496ZNF71chr19

57112959

+HSPB8chr12

119624830

+
3UTR-3CDSENST00000594944ENST00000281938ZNF71chr19

57112959

+HSPB8chr12

119624830

+
3UTR-3UTRENST00000594944ENST00000542496ZNF71chr19

57112959

+HSPB8chr12

119624830

+

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FusionProtFeatures for ZNF71_HSPB8


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ZNF71

Q9NQZ8

HSPB8

Q9UJY1

May be involved in transcriptional regulation. Displays temperature-dependent chaperone activity.

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 ZNF71_HSPB8


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 ZNF71_HSPB8


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
ZNF71CSNK2B, PRKCZ, PLK1, KDM1A, RIN3, SSX2IP, ZFP2, HIST1H1A, HIST1H1T, ZNF75A, RPS27A, ZNF7, RPL36AL, ZNF354A, KIAA0020, CENPI, RRP8, FBXO11, CENPN, WDR36, ZFP62, PWP2, ZNF70, ZNF22, RPL26L1, DDX31, POP1, FTSJ3, ZAK, NVL, DHX30, ZBTB24, DKC1, DDX27, RPL18A, CENPU, ZNF445, RPL17, ZNF184HSPB8HSPB1, HSPB7, BAG3, HSPB8, HSPB2, HSPB6, CRYAB, HSPB3, SNCA, CIAPIN1, DSTN, ASB4, DUSP12, QRICH1, KCTD13, DNAJB6, XPO1, KIF11, LONRF2, NUDT12, BRCA2, FAM83H, ACAD11, SETD2, VWA8, ZNF92, EEF1A2, RFX1, ALMS1, EXPH5, WDR20, ESR1


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 ZNF71_HSPB8


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 ZNF71_HSPB8


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneHSPB8C1834692NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA2CTD_human;UNIPROT