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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:NLRP12-SEL1L (FusionGDB2 ID:59380)

Fusion Gene Summary for NLRP12-SEL1L

check button Fusion gene summary
Fusion gene informationFusion gene name: NLRP12-SEL1L
Fusion gene ID: 59380
HgeneTgene
Gene symbol

NLRP12

SEL1L

Gene ID

91662

6400

Gene nameNLR family pyrin domain containing 12SEL1L adaptor subunit of ERAD E3 ubiquitin ligase
SynonymsCLR19.3|FCAS2|NALP12|PAN6|PYPAF7|RNO|RNO2Hrd3|PRO1063|SEL1-LIKE|SEL1L1
Cytomap

19q13.42

14q31.1

Type of geneprotein-codingprotein-coding
DescriptionNACHT, LRR and PYD domains-containing protein 12PYRIN-containing APAF1-like protein 7monarch 1nucleotide-binding oligomerization domain, leucine rich repeat and pyrin domain containing 12regulated by nitric oxideprotein sel-1 homolog 1SEL1L, ERAD E3 ligase adaptor subunitSuppressor of lin 12 (sel-1), C. elegans, homolog ofsel-1 suppressor of lin-12-like 1suppressor of lin-12-like protein 1
Modification date2020031320200313
UniProtAcc

P59046

.
Ensembl transtripts involved in fusion geneENST00000324134, ENST00000345770, 
ENST00000351894, ENST00000354278, 
ENST00000391772, ENST00000391773, 
ENST00000391775, ENST00000535162, 
ENST00000336735, ENST00000555824, 
Fusion gene scores* DoF score3 X 3 X 1=96 X 7 X 2=84
# samples 37
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(7/84*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NLRP12 [Title/Abstract] AND SEL1L [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNLRP12(54309936)-SEL1L(81939264), # 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
HgeneNLRP12

GO:0009968

negative regulation of signal transduction

16203735

HgeneNLRP12

GO:0031953

negative regulation of protein autophosphorylation

16203735

HgeneNLRP12

GO:0032088

negative regulation of NF-kappaB transcription factor activity

18230725

HgeneNLRP12

GO:0043122

regulation of I-kappaB kinase/NF-kappaB signaling

12019269

HgeneNLRP12

GO:0043124

negative regulation of I-kappaB kinase/NF-kappaB signaling

16203735

HgeneNLRP12

GO:0043281

regulation of cysteine-type endopeptidase activity involved in apoptotic process

12019269

HgeneNLRP12

GO:0045345

positive regulation of MHC class I biosynthetic process

12759408

HgeneNLRP12

GO:0045409

negative regulation of interleukin-6 biosynthetic process

16203735

HgeneNLRP12

GO:0045751

negative regulation of Toll signaling pathway

16203735

HgeneNLRP12

GO:0050710

negative regulation of cytokine secretion

16203735

HgeneNLRP12

GO:0050711

negative regulation of interleukin-1 secretion

16203735

HgeneNLRP12

GO:1901223

negative regulation of NIK/NF-kappaB signaling

17237370

HgeneNLRP12

GO:1901224

positive regulation of NIK/NF-kappaB signaling

12019269


check buttonFusion gene breakpoints across NLRP12 (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 SEL1L (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
ChiTaRS5.0N/ABI495162NLRP12chr19

54309936

-SEL1Lchr14

81939264

+


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Fusion Gene ORF analysis for NLRP12-SEL1L

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-3UTRENST00000324134ENST00000336735NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-3UTRENST00000345770ENST00000336735NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-3UTRENST00000351894ENST00000336735NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-3UTRENST00000354278ENST00000336735NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-3UTRENST00000391772ENST00000336735NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-3UTRENST00000391773ENST00000336735NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-3UTRENST00000391775ENST00000336735NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-3UTRENST00000535162ENST00000336735NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-intronENST00000324134ENST00000555824NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-intronENST00000345770ENST00000555824NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-intronENST00000351894ENST00000555824NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-intronENST00000354278ENST00000555824NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-intronENST00000391772ENST00000555824NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-intronENST00000391773ENST00000555824NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-intronENST00000391775ENST00000555824NLRP12chr19

54309936

-SEL1Lchr14

81939264

+
intron-intronENST00000535162ENST00000555824NLRP12chr19

54309936

-SEL1Lchr14

81939264

+

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 NLRP12-SEL1L


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 NLRP12-SEL1L


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/:54309936/:81939264)
- 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
NLRP12

P59046

.
FUNCTION: Plays an essential role as an potent mitigator of inflammation (PubMed:30559449). Primarily expressed in dendritic cells and macrophages, inhibits both canonical and non-canonical NF-kappa-B and ERK activation pathways (PubMed:15489334, PubMed:17947705). Functions as a negative regulator of NOD2 by targeting it to degradation via the proteasome pathway (PubMed:30559449). In turn, promotes bacterial tolerance (PubMed:30559449). Inhibits also the DDX58-mediated immune signaling against RNA viruses by reducing the E3 ubiquitin ligase TRIM25-mediated 'Lys-63'-linked DDX58 activation but enhancing the E3 ubiquitin ligase RNF125-mediated 'Lys-48'-linked DDX58 degradation (PubMed:30902577). Acts also as a negative regulator of inflammatory response to mitigate obesity and obesity-associated diseases in adipose tissue (By similarity). {ECO:0000250|UniProtKB:E9Q5R7, ECO:0000269|PubMed:15489334, ECO:0000269|PubMed:17947705, ECO:0000269|PubMed:30559449, ECO:0000269|PubMed:30902577}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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 NLRP12-SEL1L


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 NLRP12-SEL1L


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 NLRP12-SEL1L


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 NLRP12-SEL1L


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