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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:NHEJ1-ZNF124 (FusionGDB2 ID:58713)

Fusion Gene Summary for NHEJ1-ZNF124

check button Fusion gene summary
Fusion gene informationFusion gene name: NHEJ1-ZNF124
Fusion gene ID: 58713
HgeneTgene
Gene symbol

NHEJ1

ZNF124

Gene ID

79840

7678

Gene namenon-homologous end joining factor 1zinc finger protein 124
SynonymsXLFHZF-16|HZF16|ZK7
Cytomap

2q35

1q44

Type of geneprotein-codingprotein-coding
Descriptionnon-homologous end-joining factor 1XRCC4-like factornonhomologous end-joining factor 1protein cernunnoszinc finger protein 124zinc finger protein HZF-16
Modification date2020031320200313
UniProtAcc

Q9H9Q4

.
Ensembl transtripts involved in fusion geneENST00000409720, ENST00000356853, 
ENST00000483627, 
ENST00000472531, 
ENST00000491356, ENST00000340684, 
ENST00000543802, ENST00000491848, 
Fusion gene scores* DoF score4 X 4 X 4=645 X 4 X 3=60
# samples 45
** MAII scorelog2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NHEJ1 [Title/Abstract] AND ZNF124 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNHEJ1(219959996)-ZNF124(247323115), # samples:1
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
HgeneNHEJ1

GO:0010212

response to ionizing radiation

16439205


check buttonFusion gene breakpoints across NHEJ1 (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 ZNF124 (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
ChimerDB4LUSCTCGA-22-5474-01ANHEJ1chr2

219959996

-ZNF124chr1

247323115

-


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Fusion Gene ORF analysis for NHEJ1-ZNF124

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-3CDSENST00000409720ENST00000472531NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
intron-3CDSENST00000409720ENST00000491356NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
intron-3CDSENST00000409720ENST00000340684NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
intron-3CDSENST00000409720ENST00000543802NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
intron-5UTRENST00000409720ENST00000491848NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
intron-3CDSENST00000356853ENST00000472531NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
intron-3CDSENST00000356853ENST00000491356NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
intron-3CDSENST00000356853ENST00000340684NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
intron-3CDSENST00000356853ENST00000543802NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
intron-5UTRENST00000356853ENST00000491848NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
5UTR-3CDSENST00000483627ENST00000472531NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
5UTR-3CDSENST00000483627ENST00000491356NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
5UTR-3CDSENST00000483627ENST00000340684NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
5UTR-3CDSENST00000483627ENST00000543802NHEJ1chr2

219959996

-ZNF124chr1

247323115

-
5UTR-5UTRENST00000483627ENST00000491848NHEJ1chr2

219959996

-ZNF124chr1

247323115

-

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 NHEJ1-ZNF124


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 NHEJ1-ZNF124


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
NHEJ1

Q9H9Q4

.
FUNCTION: DNA repair protein involved in DNA nonhomologous end joining (NHEJ) required for double-strand break (DSB) repair and V(D)J recombination. May serve as a bridge between XRCC4 and the other NHEJ factors located at DNA ends, or may participate in reconfiguration of the end bound NHEJ factors to allow XRCC4 access to the DNA termini. It may act in concert with XRCC6/XRCC5 (Ku) to stimulate XRCC4-mediated joining of blunt ends and several types of mismatched ends that are noncomplementary or partially complementary (PubMed:16439204, PubMed:16439205, PubMed:17470781). Binds DNA in a length-dependent manner (PubMed:17317666). {ECO:0000269|PubMed:16439204, ECO:0000269|PubMed:16439205, ECO:0000269|PubMed:17317666, ECO:0000269|PubMed:17470781}.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.

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 NHEJ1-ZNF124


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 NHEJ1-ZNF124


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 NHEJ1-ZNF124


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 NHEJ1-ZNF124


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNHEJ1C1969799Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT