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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-LIN28B (FusionGDB2 ID:59379)

Fusion Gene Summary for NLRP12-LIN28B

check button Fusion gene summary
Fusion gene informationFusion gene name: NLRP12-LIN28B
Fusion gene ID: 59379
HgeneTgene
Gene symbol

NLRP12

LIN28B

Gene ID

91662

389421

Gene nameNLR family pyrin domain containing 12lin-28 homolog B
SynonymsCLR19.3|FCAS2|NALP12|PAN6|PYPAF7|RNO|RNO2CSDD2
Cytomap

19q13.42

6q16.3-q21

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 lin-28 homolog BLin-28.2lin-28B
Modification date2020031320200313
UniProtAcc

P59046

Q6ZN17

Ensembl transtripts involved in fusion geneENST00000324134, ENST00000345770, 
ENST00000351894, ENST00000354278, 
ENST00000391772, ENST00000391773, 
ENST00000391775, ENST00000535162, 
ENST00000345080, 
Fusion gene scores* DoF score3 X 3 X 1=93 X 2 X 1=6
# samples 33
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(3/6*10)=2.32192809488736
Context

PubMed: NLRP12 [Title/Abstract] AND LIN28B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointNLRP12(54309935)-LIN28B(105531207), # 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

TgeneLIN28B

GO:0050779

RNA destabilization

18951094

TgeneLIN28B

GO:2000632

negative regulation of pre-miRNA processing

18951094

TgeneLIN28B

GO:2000635

negative regulation of primary miRNA processing

18951094


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 LIN28B (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/ABI492067NLRP12chr19

54309935

-LIN28Bchr6

105531207

-


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Fusion Gene ORF analysis for NLRP12-LIN28B

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-intronENST00000324134ENST00000345080NLRP12chr19

54309935

-LIN28Bchr6

105531207

-
intron-intronENST00000345770ENST00000345080NLRP12chr19

54309935

-LIN28Bchr6

105531207

-
intron-intronENST00000351894ENST00000345080NLRP12chr19

54309935

-LIN28Bchr6

105531207

-
intron-intronENST00000354278ENST00000345080NLRP12chr19

54309935

-LIN28Bchr6

105531207

-
intron-intronENST00000391772ENST00000345080NLRP12chr19

54309935

-LIN28Bchr6

105531207

-
intron-intronENST00000391773ENST00000345080NLRP12chr19

54309935

-LIN28Bchr6

105531207

-
intron-intronENST00000391775ENST00000345080NLRP12chr19

54309935

-LIN28Bchr6

105531207

-
intron-intronENST00000535162ENST00000345080NLRP12chr19

54309935

-LIN28Bchr6

105531207

-

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-LIN28B


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-LIN28B


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/:54309935/:105531207)
- 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

LIN28B

Q6ZN17

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: Suppressor of microRNA (miRNA) biogenesis, including that of let-7 and possibly of miR107, miR-143 and miR-200c. Binds primary let-7 transcripts (pri-let-7), including pri-let-7g and pri-let-7a-1, and sequester them in the nucleolus, away from the microprocessor complex, hence preventing their processing into mature miRNA (PubMed:22118463). Does not act on pri-miR21 (PubMed:22118463). The repression of let-7 expression is required for normal development and contributes to maintain the pluripotent state of embryonic stem cells by preventing let-7-mediated differentiation. When overexpressed, recruits ZCCHC11/TUT4 uridylyltransferase to pre-let-7 transcripts, leading to their terminal uridylation and degradation (PubMed:19703396). This activity might not be relevant in vivo, as LIN28B-mediated inhibition of let-7 miRNA maturation appears to be ZCCHC11-independent (PubMed:22118463). Interaction with target pre-miRNAs occurs via an 5'-GGAG-3' motif in the pre-miRNA terminal loop. Mediates MYC-induced let-7 repression (By similarity). When overexpressed, isoform 1 stimulates growth of the breast adenocarcinoma cell line MCF-7. Isoform 2 has no effect on cell growth. {ECO:0000250|UniProtKB:Q45KJ6, ECO:0000269|PubMed:16971064, ECO:0000269|PubMed:18951094, ECO:0000269|PubMed:19703396, ECO:0000269|PubMed:22118463}.

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-LIN28B


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-LIN28B


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-LIN28B


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-LIN28B


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