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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:ZNF43-NCOR1 (FusionGDB2 ID:101393)

Fusion Gene Summary for ZNF43-NCOR1

check button Fusion gene summary
Fusion gene informationFusion gene name: ZNF43-NCOR1
Fusion gene ID: 101393
HgeneTgene
Gene symbol

ZNF43

NCOR1

Gene ID

7594

9611

Gene namezinc finger protein 43nuclear receptor corepressor 1
SynonymsHTF6|KOX27|ZNF39L1N-CoR|N-CoR1|PPP1R109|TRAC1|hN-CoR
Cytomap

19p12

17p12-p11.2

Type of geneprotein-codingprotein-coding
Descriptionzinc finger protein 43zinc finger protein 39-like 1 (KOX 27)zinc finger protein HTF6zinc finger protein KOX27nuclear receptor corepressor 1protein phosphatase 1, regulatory subunit 109thyroid hormone- and retinoic acid receptor-associated corepressor 1
Modification date2020031320200313
UniProtAcc.

O75376

Ensembl transtripts involved in fusion geneENST00000594012, ENST00000595461, 
ENST00000598381, ENST00000598288, 
ENST00000354959, ENST00000599414, 
ENST00000268712, ENST00000395851, 
ENST00000395857, ENST00000395848, 
ENST00000583226, 
Fusion gene scores* DoF score13 X 9 X 8=93614 X 14 X 6=1176
# samples 1214
** MAII scorelog2(12/936*10)=-2.96347412397489
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/1176*10)=-3.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZNF43 [Title/Abstract] AND NCOR1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointZNF43(22034706)-NCOR1(16012226), # samples:2
Anticipated loss of major functional domain due to fusion event.
* 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
TgeneNCOR1

GO:0046329

negative regulation of JNK cascade

11931768


check buttonFusion gene breakpoints across ZNF43 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across NCOR1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4ESCATCGA-L5-A893ZNF43chr19

22034706

-NCOR1chr17

16012226

-
ChimerDB4ESCATCGA-L5-A893ZNF43chr19

22034706

-NCOR1chr17

16012226

-


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Fusion Gene ORF analysis for ZNF43-NCOR1

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-3CDSENST00000594012ENST00000268712ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-3CDSENST00000594012ENST00000395851ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-intronENST00000594012ENST00000395857ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-intronENST00000594012ENST00000395848ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-5UTRENST00000594012ENST00000583226ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-3CDSENST00000595461ENST00000268712ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-3CDSENST00000595461ENST00000395851ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-intronENST00000595461ENST00000395857ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-intronENST00000595461ENST00000395848ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-5UTRENST00000595461ENST00000583226ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-3CDSENST00000598381ENST00000268712ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-3CDSENST00000598381ENST00000395851ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-intronENST00000598381ENST00000395857ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-intronENST00000598381ENST00000395848ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-5UTRENST00000598381ENST00000583226ZNF43chr19

22034706

-NCOR1chr17

16012226

-
intron-3CDSENST00000598288ENST00000268712ZNF43chr19

22034706

-NCOR1chr17

16012226

-
intron-3CDSENST00000598288ENST00000395851ZNF43chr19

22034706

-NCOR1chr17

16012226

-
intron-intronENST00000598288ENST00000395857ZNF43chr19

22034706

-NCOR1chr17

16012226

-
intron-intronENST00000598288ENST00000395848ZNF43chr19

22034706

-NCOR1chr17

16012226

-
intron-5UTRENST00000598288ENST00000583226ZNF43chr19

22034706

-NCOR1chr17

16012226

-
intron-3CDSENST00000354959ENST00000268712ZNF43chr19

22034706

-NCOR1chr17

16012226

-
intron-3CDSENST00000354959ENST00000395851ZNF43chr19

22034706

-NCOR1chr17

16012226

-
intron-intronENST00000354959ENST00000395857ZNF43chr19

22034706

-NCOR1chr17

16012226

-
intron-intronENST00000354959ENST00000395848ZNF43chr19

22034706

-NCOR1chr17

16012226

-
intron-5UTRENST00000354959ENST00000583226ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-3CDSENST00000599414ENST00000268712ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-3CDSENST00000599414ENST00000395851ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-intronENST00000599414ENST00000395857ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-intronENST00000599414ENST00000395848ZNF43chr19

22034706

-NCOR1chr17

16012226

-
5UTR-5UTRENST00000599414ENST00000583226ZNF43chr19

22034706

-NCOR1chr17

16012226

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for ZNF43-NCOR1


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for ZNF43-NCOR1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.NCOR1

O75376

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Mediates transcriptional repression by certain nuclear receptors (PubMed:20812024). Part of a complex which promotes histone deacetylation and the formation of repressive chromatin structures which may impede the access of basal transcription factors. Participates in the transcriptional repressor activity produced by BCL6. Recruited by ZBTB7A to the androgen response elements/ARE on target genes, negatively regulates androgen receptor signaling and androgen-induced cell proliferation (PubMed:20812024). Mediates the NR1D1-dependent repression and circadian regulation of TSHB expression (By similarity). The NCOR1-HDAC3 complex regulates the circadian expression of the core clock gene ARTNL/BMAL1 and the genes involved in lipid metabolism in the liver (By similarity). {ECO:0000250|UniProtKB:Q60974, ECO:0000269|PubMed:14527417, ECO:0000269|PubMed:20812024}.

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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Fusion Gene Sequence for ZNF43-NCOR1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for ZNF43-NCOR1


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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Related Drugs for ZNF43-NCOR1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for ZNF43-NCOR1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneNCOR1C0005684Malignant neoplasm of urinary bladder1CTD_human
TgeneNCOR1C0005695Bladder Neoplasm1CTD_human
TgeneNCOR1C0006142Malignant neoplasm of breast1CGI;CTD_human
TgeneNCOR1C0007138Carcinoma, Transitional Cell1CTD_human
TgeneNCOR1C0014175Endometriosis1CTD_human
TgeneNCOR1C0017636Glioblastoma1CTD_human
TgeneNCOR1C0023903Liver neoplasms1CTD_human
TgeneNCOR1C0033578Prostatic Neoplasms1CTD_human
TgeneNCOR1C0269102Endometrioma1CTD_human
TgeneNCOR1C0334588Giant Cell Glioblastoma1CTD_human
TgeneNCOR1C0345904Malignant neoplasm of liver1CTD_human
TgeneNCOR1C0376358Malignant neoplasm of prostate1CTD_human
TgeneNCOR1C0678222Breast Carcinoma1CGI;CTD_human
TgeneNCOR1C0857007Hyperbilirubinemia, Neonatal1CTD_human
TgeneNCOR1C1257931Mammary Neoplasms, Human1CTD_human
TgeneNCOR1C1458155Mammary Neoplasms1CTD_human
TgeneNCOR1C1565885Direct Hyperbilirubinemia, Neonatal1CTD_human
TgeneNCOR1C1565886Indirect Hyperbilirubinemia, Neonatal1CTD_human
TgeneNCOR1C1621958Glioblastoma Multiforme1CTD_human
TgeneNCOR1C4704874Mammary Carcinoma, Human1CTD_human