FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact
Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:AGRN-NOC4L (FusionGDB2 ID:3003)

Fusion Gene Summary for AGRN-NOC4L

check button Fusion gene summary
Fusion gene informationFusion gene name: AGRN-NOC4L
Fusion gene ID: 3003
HgeneTgene
Gene symbol

AGRN

NOC4L

Gene ID

375790

79050

Gene nameagrinnucleolar complex associated 4 homolog
SynonymsAGRIN|CMS8|CMSPPDNET49|NOC4|UTP19
Cytomap

1p36.33

12q24.33

Type of geneprotein-codingprotein-coding
Descriptionagrinagrin proteoglycannucleolar complex protein 4 homologNOC4 protein homologNOC4-like proteinnucleolar complex-associated protein 4-like protein
Modification date2020031520200313
UniProtAcc

O00468

Q9BVI4

Ensembl transtripts involved in fusion geneENST00000477585, ENST00000379370, 
ENST00000330579, ENST00000538784, 
ENST00000535343, 
Fusion gene scores* DoF score14 X 7 X 10=98036 X 4 X 20=2880
# samples 1841
** MAII scorelog2(18/980*10)=-2.4447848426729
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(41/2880*10)=-2.81237299682423
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: AGRN [Title/Abstract] AND NOC4L [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointAGRN(970704)-NOC4L(132635526), # 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
HgeneAGRN

GO:0043113

receptor clustering

15340048


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

check buttonFusion gene breakpoints across NOC4L (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4BRCATCGA-BH-A0DK-01AAGRNchr1

970704

-NOC4Lchr12

132635526

+
ChimerDB4KIRCTCGA-B8-A54I-01AAGRNchr1

957842

+NOC4Lchr12

132635526

+
ChimerDB4LUSCTCGA-39-5029-01AAGRNchr1

970704

-NOC4Lchr12

132635526

+
ChimerDB4STADTCGA-CG-5723AGRNchr1

970704

+NOC4Lchr12

132635525

+


Top

Fusion Gene ORF analysis for AGRN-NOC4L

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-3CDSENST00000477585ENST00000330579AGRNchr1

970704

-NOC4Lchr12

132635526

+
3UTR-3CDSENST00000477585ENST00000330579AGRNchr1

970704

+NOC4Lchr12

132635525

+
3UTR-5UTRENST00000477585ENST00000538784AGRNchr1

970704

-NOC4Lchr12

132635526

+
3UTR-5UTRENST00000477585ENST00000538784AGRNchr1

970704

+NOC4Lchr12

132635525

+
3UTR-intronENST00000477585ENST00000535343AGRNchr1

970704

-NOC4Lchr12

132635526

+
3UTR-intronENST00000477585ENST00000535343AGRNchr1

970704

+NOC4Lchr12

132635525

+
5CDS-5UTRENST00000379370ENST00000538784AGRNchr1

957842

+NOC4Lchr12

132635526

+
5CDS-5UTRENST00000379370ENST00000538784AGRNchr1

970704

-NOC4Lchr12

132635526

+
5CDS-5UTRENST00000379370ENST00000538784AGRNchr1

970704

+NOC4Lchr12

132635525

+
5CDS-intronENST00000379370ENST00000535343AGRNchr1

957842

+NOC4Lchr12

132635526

+
5CDS-intronENST00000379370ENST00000535343AGRNchr1

970704

-NOC4Lchr12

132635526

+
5CDS-intronENST00000379370ENST00000535343AGRNchr1

970704

+NOC4Lchr12

132635525

+
In-frameENST00000379370ENST00000330579AGRNchr1

957842

+NOC4Lchr12

132635526

+
In-frameENST00000379370ENST00000330579AGRNchr1

970704

-NOC4Lchr12

132635526

+
In-frameENST00000379370ENST00000330579AGRNchr1

970704

+NOC4Lchr12

132635525

+
intron-3CDSENST00000477585ENST00000330579AGRNchr1

957842

+NOC4Lchr12

132635526

+
intron-5UTRENST00000477585ENST00000538784AGRNchr1

957842

+NOC4Lchr12

132635526

+
intron-intronENST00000477585ENST00000535343AGRNchr1

957842

+NOC4Lchr12

132635526

+

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)
ENST00000379370AGRNchr1970704+ENST00000330579NOC4Lchr12132635525+125156111922397
ENST00000379370AGRNchr1957842+ENST00000330579NOC4Lchr12132635526+120351311442381
ENST00000379370AGRNchr1970704-ENST00000330579NOC4Lchr12132635526+125156111922397

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
ENST00000379370ENST00000330579AGRNchr1970704+NOC4Lchr12132635525+0.012241190.9877588
ENST00000379370ENST00000330579AGRNchr1957842+NOC4Lchr12132635526+0.0085797570.99142027
ENST00000379370ENST00000330579AGRNchr1970704-NOC4Lchr12132635526+0.012241190.9877588

Top

Fusion Genomic Features for AGRN-NOC4L


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)
AGRNchr1970704+NOC4Lchr12132635525+0.0007394360.9992606
AGRNchr1957842+NOC4Lchr12132635525+8.00E-060.999992
AGRNchr1970704+NOC4Lchr12132635525+0.0007394360.9992606
AGRNchr1957842+NOC4Lchr12132635525+8.00E-060.999992

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.
genomic feature

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.
genomic feature of top 1%

Top

Fusion Protein Features for AGRN-NOC4L


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr1:970704/chr12:132635526)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

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

O00468

NOC4L

Q9BVI4

FUNCTION: [Isoform 1]: heparan sulfate basal lamina glycoprotein that plays a central role in the formation and the maintenance of the neuromuscular junction (NMJ) and directs key events in postsynaptic differentiation. Component of the AGRN-LRP4 receptor complex that induces the phosphorylation and activation of MUSK. The activation of MUSK in myotubes induces the formation of NMJ by regulating different processes including the transcription of specific genes and the clustering of AChR in the postsynaptic membrane. Calcium ions are required for maximal AChR clustering. AGRN function in neurons is highly regulated by alternative splicing, glycan binding and proteolytic processing. Modulates calcium ion homeostasis in neurons, specifically by inducing an increase in cytoplasmic calcium ions. Functions differentially in the central nervous system (CNS) by inhibiting the alpha(3)-subtype of Na+/K+-ATPase and evoking depolarization at CNS synapses. This secreted isoform forms a bridge, after release from motor neurons, to basal lamina through binding laminin via the NtA domain.; FUNCTION: [Isoform 2]: transmembrane form that is the predominate form in neurons of the brain, induces dendritic filopodia and synapse formation in mature hippocampal neurons in large part due to the attached glycosaminoglycan chains and the action of Rho-family GTPases.; FUNCTION: Isoform 1, isoform 4 and isoform 5: neuron-specific (z+) isoforms that contain C-terminal insertions of 8-19 AA are potent activators of AChR clustering. Isoform 5, agrin (z+8), containing the 8-AA insert, forms a receptor complex in myotubules containing the neuronal AGRN, the muscle-specific kinase MUSK and LRP4, a member of the LDL receptor family. The splicing factors, NOVA1 and NOVA2, regulate AGRN splicing and production of the 'z' isoforms.; FUNCTION: Isoform 3 and isoform 6: lack any 'z' insert, are muscle-specific and may be involved in endothelial cell differentiation.; FUNCTION: [Agrin N-terminal 110 kDa subunit]: is involved in regulation of neurite outgrowth probably due to the presence of the glycosaminoglcan (GAG) side chains of heparan and chondroitin sulfate attached to the Ser/Thr- and Gly/Ser-rich regions. Also involved in modulation of growth factor signaling (By similarity). {ECO:0000250, ECO:0000269|PubMed:19631309, ECO:0000269|PubMed:21969364}.; FUNCTION: [Agrin C-terminal 22 kDa fragment]: this released fragment is important for agrin signaling and to exert a maximal dendritic filopodia-inducing effect. All 'z' splice variants (z+) of this fragment also show an increase in the number of filopodia.

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
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+23630_1571542046.0DomainNtA
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+33630_1571702046.0DomainNtA
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-33630_1571702046.0DomainNtA
TgeneNOC4Lchr1:957842chr12:132635526ENST00000330579815347_367300517.0TransmembraneHelical
TgeneNOC4Lchr1:957842chr12:132635526ENST00000330579815375_395300517.0TransmembraneHelical
TgeneNOC4Lchr1:970704chr12:132635525ENST00000330579815347_367300517.0TransmembraneHelical
TgeneNOC4Lchr1:970704chr12:132635525ENST00000330579815375_395300517.0TransmembraneHelical
TgeneNOC4Lchr1:970704chr12:132635526ENST00000330579815347_367300517.0TransmembraneHelical
TgeneNOC4Lchr1:970704chr12:132635526ENST00000330579815375_395300517.0TransmembraneHelical

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361941_20091542046.0Calcium bindingOntology_term=ECO:0000250
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361941_20091702046.0Calcium bindingOntology_term=ECO:0000250
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361941_20091702046.0Calcium bindingOntology_term=ECO:0000250
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361058_10971542046.0Compositional biasNote=Gly/Ser-rich
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361254_13241542046.0Compositional biasNote=Ser/Thr-rich
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236671_6771542046.0Compositional biasNote=Gly/Ser-rich
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236974_10991542046.0Compositional biasNote=Ser/Thr-rich
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361058_10971702046.0Compositional biasNote=Gly/Ser-rich
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361254_13241702046.0Compositional biasNote=Ser/Thr-rich
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336671_6771702046.0Compositional biasNote=Gly/Ser-rich
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336974_10991702046.0Compositional biasNote=Ser/Thr-rich
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361058_10971702046.0Compositional biasNote=Gly/Ser-rich
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361254_13241702046.0Compositional biasNote=Ser/Thr-rich
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336671_6771702046.0Compositional biasNote=Gly/Ser-rich
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336974_10991702046.0Compositional biasNote=Ser/Thr-rich
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361130_12521542046.0DomainSEA
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361329_13671542046.0DomainEGF-like 1
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361372_15481542046.0DomainLaminin G-like 1
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361549_15861542046.0DomainEGF-like 2
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361588_16251542046.0DomainEGF-like 3
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361635_18221542046.0DomainLaminin G-like 2
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361818_18571542046.0DomainEGF-like 4
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+2361868_20651542046.0DomainLaminin G-like 3
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236191_2441542046.0DomainKazal-like 1
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236264_3191542046.0DomainKazal-like 2
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236337_3911542046.0DomainKazal-like 3
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236408_4631542046.0DomainKazal-like 4
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236484_5361542046.0DomainKazal-like 5
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236540_6011542046.0DomainKazal-like 6
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236607_6661542046.0DomainKazal-like 7
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236699_7521542046.0DomainKazal-like 8
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236793_8461542046.0DomainLaminin EGF-like 1
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236847_8931542046.0DomainLaminin EGF-like 2
HgeneAGRNchr1:957842chr12:132635526ENST00000379370+236917_9711542046.0DomainKazal-like 9
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361130_12521702046.0DomainSEA
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361329_13671702046.0DomainEGF-like 1
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361372_15481702046.0DomainLaminin G-like 1
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361549_15861702046.0DomainEGF-like 2
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361588_16251702046.0DomainEGF-like 3
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361635_18221702046.0DomainLaminin G-like 2
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361818_18571702046.0DomainEGF-like 4
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+3361868_20651702046.0DomainLaminin G-like 3
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336191_2441702046.0DomainKazal-like 1
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336264_3191702046.0DomainKazal-like 2
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336337_3911702046.0DomainKazal-like 3
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336408_4631702046.0DomainKazal-like 4
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336484_5361702046.0DomainKazal-like 5
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336540_6011702046.0DomainKazal-like 6
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336607_6661702046.0DomainKazal-like 7
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336699_7521702046.0DomainKazal-like 8
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336793_8461702046.0DomainLaminin EGF-like 1
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336847_8931702046.0DomainLaminin EGF-like 2
HgeneAGRNchr1:970704chr12:132635525ENST00000379370+336917_9711702046.0DomainKazal-like 9
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361130_12521702046.0DomainSEA
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361329_13671702046.0DomainEGF-like 1
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361372_15481702046.0DomainLaminin G-like 1
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361549_15861702046.0DomainEGF-like 2
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361588_16251702046.0DomainEGF-like 3
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361635_18221702046.0DomainLaminin G-like 2
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361818_18571702046.0DomainEGF-like 4
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-3361868_20651702046.0DomainLaminin G-like 3
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336191_2441702046.0DomainKazal-like 1
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336264_3191702046.0DomainKazal-like 2
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336337_3911702046.0DomainKazal-like 3
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336408_4631702046.0DomainKazal-like 4
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336484_5361702046.0DomainKazal-like 5
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336540_6011702046.0DomainKazal-like 6
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336607_6661702046.0DomainKazal-like 7
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336699_7521702046.0DomainKazal-like 8
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336793_8461702046.0DomainLaminin EGF-like 1
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336847_8931702046.0DomainLaminin EGF-like 2
HgeneAGRNchr1:970704chr12:132635526ENST00000379370-336917_9711702046.0DomainKazal-like 9
TgeneNOC4Lchr1:957842chr12:132635526ENST00000330579815297_317300517.0TransmembraneHelical
TgeneNOC4Lchr1:970704chr12:132635525ENST00000330579815297_317300517.0TransmembraneHelical
TgeneNOC4Lchr1:970704chr12:132635526ENST00000330579815297_317300517.0TransmembraneHelical


Top

Fusion Gene Sequence for AGRN-NOC4L


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.
>3003_3003_1_AGRN-NOC4L_AGRN_chr1_957842_ENST00000379370_NOC4L_chr12_132635526_ENST00000330579_length(transcript)=1203nt_BP=513nt
CCCGTCCCCGGCGCGGCCCGCGCGCTCCTCCGCCGCCTCTCGCCTGCGCCATGGCCGGCCGGTCCCACCCGGGCCCGCTGCGGCCGCTGC
TGCCGCTCCTTGTGGTGGCCGCGTGCGTCCTGCCCGGAGCCGGCGGGACATGCCCGGAGCGCGCGCTGGAGCGGCGCGAGGAGGAGGCGA
ACGTGGTGCTCACCGGGACGGTGGAGGAGATCCTCAACGTGGACCCGGTGCAGCACACGTACTCCTGCAAGGTTCGGGTCTGGCGGTACT
TGAAGGGCAAAGACCTGGTGGCCCGGGAGAGCCTGCTGGACGGCGGCAACAAGGTGGTGATCAGCGGCTTTGGAGACCCCCTCATCTGTG
ACAACCAGGTGTCCACTGGGGACACCAGGATCTTCTTTGTGAACCCTGCACCCCCATACCTGTGGCCAGCCCACAAGAACGAGCTGATGC
TCAACTCCAGCCTCATGCGGATCACCCTGCGGAACCTGGAGGAGGTGGAGTTCTGTGTGGAAGGGGGGGCCCTCAGCCTCTTGGCCTTGA
ACGGGCTGTTCATCTTGATTCACAAACACAACCTGGAGTACCCTGACTTCTACCGGAAGCTCTACGGCCTCTTGGACCCCTCTGTCTTTC
ACGTCAAGTACCGCGCCCGCTTCTTCCACCTGGCTGACCTCTTCCTGTCCTCCTCCCACCTCCCCGCCTACCTGGTGGCCGCCTTCGCCA
AGCGGCTGGCCCGCCTGGCCCTGACGGCTCCCCCTGAGGCCCTGCTCATGGTCCTGCCTTTCATCTGTAACCTGCTGCGCCGGCACCCTG
CCTGCCGGGTCCTCGTGCACCGTCCACACGGCCCTGAGTTGGACGCCGACCCCTACGACCCTGGAGAGGAGGACCCAGCCCAGAGCCGGG
CCTTGGAGAGCTCCCTGTGGGAGCTTCAGGCCCTCCAGCGCCACTACCACCCTGAGGTGTCCAAAGCCGCCAGCGTCATCAACCAGGCCC
TGTCCATGCCTGAGGTCAGCATCGCGCCACTGCTGGAGCTCACGGCCTACGAGATCTTTGAGCGGGACCTGAAGAAGAAGGGGCCCGAGC
CGGTGCCACTGGAGTTTATCCCAGCCCAGGGCCTGCTGGGACGGCCGGGTGAACTCTGTGCCCAGCACTTCACGCTCAGCTGACCCTGGC

>3003_3003_1_AGRN-NOC4L_AGRN_chr1_957842_ENST00000379370_NOC4L_chr12_132635526_ENST00000330579_length(amino acids)=381AA_BP=1
MGTEFTRPSQQALGWDKLQWHRLGPLLLQVPLKDLVGRELQQWRDADLRHGQGLVDDAGGFGHLRVVVALEGLKLPQGALQGPALGWVLL
SRVVGVGVQLRAVWTVHEDPAGRVPAQQVTDERQDHEQGLRGSRQGQAGQPLGEGGHQVGGEVGGGQEEVSQVEEAGAVLDVKDRGVQEA
VELPVEVRVLQVVFVNQDEQPVQGQEAEGPPFHTELHLLQVPQGDPHEAGVEHQLVLVGWPQVWGCRVHKEDPGVPSGHLVVTDEGVSKA
ADHHLVAAVQQALPGHQVFALQVPPDPNLAGVRVLHRVHVEDLLHRPGEHHVRLLLAPLQRALRACPAGSGQDARGHHKERQQRPQRARV

--------------------------------------------------------------
>3003_3003_2_AGRN-NOC4L_AGRN_chr1_970704_ENST00000379370_NOC4L_chr12_132635525_ENST00000330579_length(transcript)=1251nt_BP=561nt
CCCGTCCCCGGCGCGGCCCGCGCGCTCCTCCGCCGCCTCTCGCCTGCGCCATGGCCGGCCGGTCCCACCCGGGCCCGCTGCGGCCGCTGC
TGCCGCTCCTTGTGGTGGCCGCGTGCGTCCTGCCCGGAGCCGGCGGGACATGCCCGGAGCGCGCGCTGGAGCGGCGCGAGGAGGAGGCGA
ACGTGGTGCTCACCGGGACGGTGGAGGAGATCCTCAACGTGGACCCGGTGCAGCACACGTACTCCTGCAAGGTTCGGGTCTGGCGGTACT
TGAAGGGCAAAGACCTGGTGGCCCGGGAGAGCCTGCTGGACGGCGGCAACAAGGTGGTGATCAGCGGCTTTGGAGACCCCCTCATCTGTG
ACAACCAGGTGTCCACTGGGGACACCAGGATCTTCTTTGTGAACCCTGCACCCCCATACCTGTGGCCAGCCCACAAGAACGAGCTGATGC
TCAACTCCAGCCTCATGCGGATCACCCTGCGGAACCTGGAGGAGGTGGAGTTCTGTGTGGAAGATAAACCCGGGACCCACTTCACTCCAG
TGCCTCCGACGCCTCCTGATGGGGGGGCCCTCAGCCTCTTGGCCTTGAACGGGCTGTTCATCTTGATTCACAAACACAACCTGGAGTACC
CTGACTTCTACCGGAAGCTCTACGGCCTCTTGGACCCCTCTGTCTTTCACGTCAAGTACCGCGCCCGCTTCTTCCACCTGGCTGACCTCT
TCCTGTCCTCCTCCCACCTCCCCGCCTACCTGGTGGCCGCCTTCGCCAAGCGGCTGGCCCGCCTGGCCCTGACGGCTCCCCCTGAGGCCC
TGCTCATGGTCCTGCCTTTCATCTGTAACCTGCTGCGCCGGCACCCTGCCTGCCGGGTCCTCGTGCACCGTCCACACGGCCCTGAGTTGG
ACGCCGACCCCTACGACCCTGGAGAGGAGGACCCAGCCCAGAGCCGGGCCTTGGAGAGCTCCCTGTGGGAGCTTCAGGCCCTCCAGCGCC
ACTACCACCCTGAGGTGTCCAAAGCCGCCAGCGTCATCAACCAGGCCCTGTCCATGCCTGAGGTCAGCATCGCGCCACTGCTGGAGCTCA
CGGCCTACGAGATCTTTGAGCGGGACCTGAAGAAGAAGGGGCCCGAGCCGGTGCCACTGGAGTTTATCCCAGCCCAGGGCCTGCTGGGAC

>3003_3003_2_AGRN-NOC4L_AGRN_chr1_970704_ENST00000379370_NOC4L_chr12_132635525_ENST00000330579_length(amino acids)=397AA_BP=1
MGTEFTRPSQQALGWDKLQWHRLGPLLLQVPLKDLVGRELQQWRDADLRHGQGLVDDAGGFGHLRVVVALEGLKLPQGALQGPALGWVLL
SRVVGVGVQLRAVWTVHEDPAGRVPAQQVTDERQDHEQGLRGSRQGQAGQPLGEGGHQVGGEVGGGQEEVSQVEEAGAVLDVKDRGVQEA
VELPVEVRVLQVVFVNQDEQPVQGQEAEGPPIRRRRRHWSEVGPGFIFHTELHLLQVPQGDPHEAGVEHQLVLVGWPQVWGCRVHKEDPG
VPSGHLVVTDEGVSKAADHHLVAAVQQALPGHQVFALQVPPDPNLAGVRVLHRVHVEDLLHRPGEHHVRLLLAPLQRALRACPAGSGQDA

--------------------------------------------------------------
>3003_3003_3_AGRN-NOC4L_AGRN_chr1_970704_ENST00000379370_NOC4L_chr12_132635526_ENST00000330579_length(transcript)=1251nt_BP=561nt
CCCGTCCCCGGCGCGGCCCGCGCGCTCCTCCGCCGCCTCTCGCCTGCGCCATGGCCGGCCGGTCCCACCCGGGCCCGCTGCGGCCGCTGC
TGCCGCTCCTTGTGGTGGCCGCGTGCGTCCTGCCCGGAGCCGGCGGGACATGCCCGGAGCGCGCGCTGGAGCGGCGCGAGGAGGAGGCGA
ACGTGGTGCTCACCGGGACGGTGGAGGAGATCCTCAACGTGGACCCGGTGCAGCACACGTACTCCTGCAAGGTTCGGGTCTGGCGGTACT
TGAAGGGCAAAGACCTGGTGGCCCGGGAGAGCCTGCTGGACGGCGGCAACAAGGTGGTGATCAGCGGCTTTGGAGACCCCCTCATCTGTG
ACAACCAGGTGTCCACTGGGGACACCAGGATCTTCTTTGTGAACCCTGCACCCCCATACCTGTGGCCAGCCCACAAGAACGAGCTGATGC
TCAACTCCAGCCTCATGCGGATCACCCTGCGGAACCTGGAGGAGGTGGAGTTCTGTGTGGAAGATAAACCCGGGACCCACTTCACTCCAG
TGCCTCCGACGCCTCCTGATGGGGGGGCCCTCAGCCTCTTGGCCTTGAACGGGCTGTTCATCTTGATTCACAAACACAACCTGGAGTACC
CTGACTTCTACCGGAAGCTCTACGGCCTCTTGGACCCCTCTGTCTTTCACGTCAAGTACCGCGCCCGCTTCTTCCACCTGGCTGACCTCT
TCCTGTCCTCCTCCCACCTCCCCGCCTACCTGGTGGCCGCCTTCGCCAAGCGGCTGGCCCGCCTGGCCCTGACGGCTCCCCCTGAGGCCC
TGCTCATGGTCCTGCCTTTCATCTGTAACCTGCTGCGCCGGCACCCTGCCTGCCGGGTCCTCGTGCACCGTCCACACGGCCCTGAGTTGG
ACGCCGACCCCTACGACCCTGGAGAGGAGGACCCAGCCCAGAGCCGGGCCTTGGAGAGCTCCCTGTGGGAGCTTCAGGCCCTCCAGCGCC
ACTACCACCCTGAGGTGTCCAAAGCCGCCAGCGTCATCAACCAGGCCCTGTCCATGCCTGAGGTCAGCATCGCGCCACTGCTGGAGCTCA
CGGCCTACGAGATCTTTGAGCGGGACCTGAAGAAGAAGGGGCCCGAGCCGGTGCCACTGGAGTTTATCCCAGCCCAGGGCCTGCTGGGAC

>3003_3003_3_AGRN-NOC4L_AGRN_chr1_970704_ENST00000379370_NOC4L_chr12_132635526_ENST00000330579_length(amino acids)=397AA_BP=1
MGTEFTRPSQQALGWDKLQWHRLGPLLLQVPLKDLVGRELQQWRDADLRHGQGLVDDAGGFGHLRVVVALEGLKLPQGALQGPALGWVLL
SRVVGVGVQLRAVWTVHEDPAGRVPAQQVTDERQDHEQGLRGSRQGQAGQPLGEGGHQVGGEVGGGQEEVSQVEEAGAVLDVKDRGVQEA
VELPVEVRVLQVVFVNQDEQPVQGQEAEGPPIRRRRRHWSEVGPGFIFHTELHLLQVPQGDPHEAGVEHQLVLVGWPQVWGCRVHKEDPG
VPSGHLVVTDEGVSKAADHHLVAAVQQALPGHQVFALQVPPDPNLAGVRVLHRVHVEDLLHRPGEHHVRLLLAPLQRALRACPAGSGQDA

--------------------------------------------------------------

Top

Fusion Gene PPI Analysis for AGRN-NOC4L


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


Top

Related Drugs for AGRN-NOC4L


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

Top

Related Diseases for AGRN-NOC4L


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