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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:PIP5K1A-NPR1 (FusionGDB2 ID:65101)

Fusion Gene Summary for PIP5K1A-NPR1

check button Fusion gene summary
Fusion gene informationFusion gene name: PIP5K1A-NPR1
Fusion gene ID: 65101
HgeneTgene
Gene symbol

PIP5K1A

NPR1

Gene ID

8394

4881

Gene namephosphatidylinositol-4-phosphate 5-kinase type 1 alphanatriuretic peptide receptor 1
Synonyms-ANPRA|ANPa|GUC2A|GUCY2A|NPRA
Cytomap

1q21.3

1q21.3

Type of geneprotein-codingprotein-coding
Descriptionphosphatidylinositol 4-phosphate 5-kinase type-1 alpha68 kDa type I phosphatidylinositol 4-phosphate 5-kinase alphaPIP5K1-alphaPIP5KIalphaphosphatidylinositol 4-phosphate 5-kinase type I alphaptdIns(4)P-5-kinase 1 alphaatrial natriuretic peptide receptor 1ANP-AANPR-AGC-ANPR-Aatrial natriuretic peptide receptor type Aatrionatriuretic peptide receptor Aguanylate cyclase Anatriuretic peptide A type receptornatriuretic peptide receptor Anatriuretic peptide recepto
Modification date2020031320200322
UniProtAcc.

P16066

Ensembl transtripts involved in fusion geneENST00000409426, ENST00000441902, 
ENST00000368890, ENST00000368888, 
ENST00000464105, ENST00000414290, 
ENST00000368680, ENST00000413826, 
Fusion gene scores* DoF score10 X 6 X 7=4201 X 1 X 1=1
# samples 111
** MAII scorelog2(11/420*10)=-1.93288580414146
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: PIP5K1A [Title/Abstract] AND NPR1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPIP5K1A(151209239)-NPR1(153655852), # samples:1
Anticipated loss of major functional domain due to fusion event.PIP5K1A-NPR1 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PIP5K1A-NPR1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
PIP5K1A-NPR1 seems lost the major protein functional domain in Tgene partner, which is a kinase due to the frame-shifted ORF.
PIP5K1A-NPR1 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PIP5K1A-NPR1 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
* 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
HgenePIP5K1A

GO:0008654

phospholipid biosynthetic process

15157668

TgeneNPR1

GO:0006182

cGMP biosynthetic process

1672777

TgeneNPR1

GO:0007168

receptor guanylyl cyclase signaling pathway

1672777


check buttonFusion gene breakpoints across PIP5K1A (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 NPR1 (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
ChimerDB4GBMTCGA-19-2619-01APIP5K1Achr1

151209239

+NPR1chr1

153655852

+


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Fusion Gene ORF analysis for PIP5K1A-NPR1

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
Frame-shiftENST00000409426ENST00000368680PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
5CDS-intronENST00000409426ENST00000413826PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
Frame-shiftENST00000441902ENST00000368680PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
5CDS-intronENST00000441902ENST00000413826PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
Frame-shiftENST00000368890ENST00000368680PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
5CDS-intronENST00000368890ENST00000413826PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
Frame-shiftENST00000368888ENST00000368680PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
5CDS-intronENST00000368888ENST00000413826PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
intron-3CDSENST00000464105ENST00000368680PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
intron-intronENST00000464105ENST00000413826PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
Frame-shiftENST00000414290ENST00000368680PIP5K1Achr1

151209239

+NPR1chr1

153655852

+
5CDS-intronENST00000414290ENST00000413826PIP5K1Achr1

151209239

+NPR1chr1

153655852

+

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 PIP5K1A-NPR1


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)
PIP5K1Achr1151209239+NPR1chr1153655851+0.0096579040.99034214
PIP5K1Achr1151209239+NPR1chr1153655851+0.0096579040.99034214

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 PIP5K1A-NPR1


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
.NPR1

P16066

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: Receptor for the atrial natriuretic peptide NPPA/ANP and the brain natriuretic peptide NPPB/BNP which are potent vasoactive hormones playing a key role in cardiovascular homeostasis. Has guanylate cyclase activity upon binding of the ligand. {ECO:0000269|PubMed:1672777}.

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 PIP5K1A-NPR1


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 PIP5K1A-NPR1


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 PIP5K1A-NPR1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneNPR1P16066DB01612Amyl NitriteAgonistSmall moleculeApproved
TgeneNPR1P16066DB01612Amyl NitriteAgonistSmall moleculeApproved
TgeneNPR1P16066DB01613Erythrityl tetranitrateAgonistSmall moleculeApproved|Experimental|Investigational
TgeneNPR1P16066DB01613Erythrityl tetranitrateAgonistSmall moleculeApproved|Experimental|Investigational
TgeneNPR1P16066DB00325NitroprussideAgonistSmall moleculeApproved|Investigational
TgeneNPR1P16066DB00325NitroprussideAgonistSmall moleculeApproved|Investigational
TgeneNPR1P16066DB00727NitroglycerinAgonistSmall moleculeApproved|Investigational
TgeneNPR1P16066DB00727NitroglycerinAgonistSmall moleculeApproved|Investigational
TgeneNPR1P16066DB00883Isosorbide dinitrateAgonistSmall moleculeApproved|Investigational
TgeneNPR1P16066DB00883Isosorbide dinitrateAgonistSmall moleculeApproved|Investigational
TgeneNPR1P16066DB04899NesiritideBinderBiotechApproved|Investigational
TgeneNPR1P16066DB04899NesiritideBinderBiotechApproved|Investigational

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Related Diseases for PIP5K1A-NPR1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneNPR1C0016059Fibrosis1CTD_human
TgeneNPR1C0018800Cardiomegaly1CTD_human
TgeneNPR1C0018801Heart failure1CTD_human
TgeneNPR1C0018802Congestive heart failure1CTD_human
TgeneNPR1C0020538Hypertensive disease1CTD_human
TgeneNPR1C0022658Kidney Diseases1CTD_human
TgeneNPR1C0023212Left-Sided Heart Failure1CTD_human
TgeneNPR1C0030193Pain1CTD_human
TgeneNPR1C0234230Pain, Burning1CTD_human
TgeneNPR1C0234238Ache1CTD_human
TgeneNPR1C0234254Radiating pain1CTD_human
TgeneNPR1C0235527Heart Failure, Right-Sided1CTD_human
TgeneNPR1C0236664Alcohol-Related Disorders1PSYGENET
TgeneNPR1C0458257Pain, Splitting1CTD_human
TgeneNPR1C0458259Pain, Crushing1CTD_human
TgeneNPR1C0751407Pain, Migratory1CTD_human
TgeneNPR1C0751408Suffering, Physical1CTD_human
TgeneNPR1C1383860Cardiac Hypertrophy1CTD_human
TgeneNPR1C1623038Cirrhosis1CTD_human
TgeneNPR1C1959583Myocardial Failure1CTD_human
TgeneNPR1C1961112Heart Decompensation1CTD_human