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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:SERPINI1-NAALADL2 (FusionGDB2 ID:80244)

Fusion Gene Summary for SERPINI1-NAALADL2

check button Fusion gene summary
Fusion gene informationFusion gene name: SERPINI1-NAALADL2
Fusion gene ID: 80244
HgeneTgene
Gene symbol

SERPINI1

NAALADL2

Gene ID

5274

254827

Gene nameserpin family I member 1N-acetylated alpha-linked acidic dipeptidase like 2
SynonymsPI12|neuroserpin-
Cytomap

3q26.1

3q26.31

Type of geneprotein-codingprotein-coding
DescriptionneuroserpinPI-12peptidase inhibitor 12serine (or cysteine) proteinase inhibitor, clade I (neuroserpin), member 1serpin I1serpin peptidase inhibitor clade I member 1serpin peptidase inhibitor, clade I (neuroserpin), member 1inactive N-acetylated-alpha-linked acidic dipeptidase-like protein 2N-acetylated alpha-linked acidic dipeptidase 2NAALADase L2glutamate carboxypeptidase II-type non-peptidase homologue
Modification date2020031320200313
UniProtAcc.

Q58DX5

Ensembl transtripts involved in fusion geneENST00000446050, ENST00000295777, 
ENST00000488374, 
ENST00000454872, 
ENST00000473253, 
Fusion gene scores* DoF score1 X 1 X 1=121 X 16 X 9=3024
# samples 124
** MAII scorelog2(1/1*10)=3.32192809488736log2(24/3024*10)=-3.65535182861255
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SERPINI1 [Title/Abstract] AND NAALADL2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSERPINI1(167453611)-NAALADL2(174814580), # 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

check buttonFusion gene breakpoints across SERPINI1 (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 NAALADL2 (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
ChimerDB4BRCATCGA-A8-A081-01ASERPINI1chr3

167453611

-NAALADL2chr3

174814580

+


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Fusion Gene ORF analysis for SERPINI1-NAALADL2

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-3CDSENST00000446050ENST00000454872SERPINI1chr3

167453611

-NAALADL2chr3

174814580

+
5UTR-3UTRENST00000446050ENST00000473253SERPINI1chr3

167453611

-NAALADL2chr3

174814580

+
5UTR-3CDSENST00000295777ENST00000454872SERPINI1chr3

167453611

-NAALADL2chr3

174814580

+
5UTR-3UTRENST00000295777ENST00000473253SERPINI1chr3

167453611

-NAALADL2chr3

174814580

+
intron-3CDSENST00000488374ENST00000454872SERPINI1chr3

167453611

-NAALADL2chr3

174814580

+
intron-3UTRENST00000488374ENST00000473253SERPINI1chr3

167453611

-NAALADL2chr3

174814580

+

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 SERPINI1-NAALADL2


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 SERPINI1-NAALADL2


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
.NAALADL2

Q58DX5

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: May be catalytically inactive.

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 SERPINI1-NAALADL2


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 SERPINI1-NAALADL2


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 SERPINI1-NAALADL2


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 SERPINI1-NAALADL2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSERPINI1C1858680Familial encephalopathy with neuroserpin inclusion bodies3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneSERPINI1C0036341Schizophrenia1PSYGENET
HgeneSERPINI1C0751776Atypical Inclusion-Body Disease1CTD_human
HgeneSERPINI1C0751777Familial Progressive Myoclonic Epilepsy1CTD_human
HgeneSERPINI1C0751778Myoclonic Epilepsies, Progressive1CTD_human
HgeneSERPINI1C0751779Action Myoclonus-Renal Failure Syndrome1CTD_human
HgeneSERPINI1C0751780Biotin-Responsive Encephalopathy1CTD_human
HgeneSERPINI1C0751781Dentatorubral-Pallidoluysian Atrophy1CTD_human
HgeneSERPINI1C0751782May-White Syndrome1CTD_human