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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:PENK-CHGB (FusionGDB2 ID:63873)

Fusion Gene Summary for PENK-CHGB

check button Fusion gene summary
Fusion gene informationFusion gene name: PENK-CHGB
Fusion gene ID: 63873
HgeneTgene
Gene symbol

PENK

CHGB

Gene ID

5179

1114

Gene nameproenkephalinchromogranin B
SynonymsPE|PENK-ASCG1
Cytomap

8q12.1

20p12.3

Type of geneprotein-codingprotein-coding
Descriptionproenkephalin-Aenkephalin Apeptide Fpreproenkephalinsecretogranin-1cgBsecretogranin Bsecretogranin IsgI
Modification date2020031520200313
UniProtAcc.

P05060

Ensembl transtripts involved in fusion geneENST00000314922, ENST00000451791, 
ENST00000523274, ENST00000523051, 
ENST00000518770, 
ENST00000378961, 
ENST00000488832, 
Fusion gene scores* DoF score2 X 2 X 1=48 X 11 X 4=352
# samples 210
** MAII scorelog2(2/4*10)=2.32192809488736log2(10/352*10)=-1.81557542886257
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PENK [Title/Abstract] AND CHGB [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCHGB(5904003)-PENK(57354090), # samples:1
PENK(57354194)-CHGB(5903946), # 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 PENK (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 CHGB (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
ChimerDB4PCPGTCGA-QT-A5XO-01APENKchr8

57354194

-CHGBchr20

5903946

+


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Fusion Gene ORF analysis for PENK-CHGB

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-3CDSENST00000314922ENST00000378961PENKchr8

57354194

-CHGBchr20

5903946

+
intron-intronENST00000314922ENST00000488832PENKchr8

57354194

-CHGBchr20

5903946

+
intron-3CDSENST00000451791ENST00000378961PENKchr8

57354194

-CHGBchr20

5903946

+
intron-intronENST00000451791ENST00000488832PENKchr8

57354194

-CHGBchr20

5903946

+
intron-3CDSENST00000523274ENST00000378961PENKchr8

57354194

-CHGBchr20

5903946

+
intron-intronENST00000523274ENST00000488832PENKchr8

57354194

-CHGBchr20

5903946

+
intron-3CDSENST00000523051ENST00000378961PENKchr8

57354194

-CHGBchr20

5903946

+
intron-intronENST00000523051ENST00000488832PENKchr8

57354194

-CHGBchr20

5903946

+
intron-3CDSENST00000518770ENST00000378961PENKchr8

57354194

-CHGBchr20

5903946

+
intron-intronENST00000518770ENST00000488832PENKchr8

57354194

-CHGBchr20

5903946

+

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 PENK-CHGB


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 PENK-CHGB


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
.CHGB

P05060

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: Secretogranin-1 is a neuroendocrine secretory granule protein, which may be the precursor for other biologically active peptides.

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 PENK-CHGB


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 PENK-CHGB


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 PENK-CHGB


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 PENK-CHGB


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgenePENKC0011570Mental Depression4PSYGENET
HgenePENKC0011581Depressive disorder4PSYGENET
HgenePENKC0024809Marijuana Abuse3PSYGENET
HgenePENKC0006870Cannabis Dependence1PSYGENET
HgenePENKC0013386Dyskinesia, Drug-Induced1CTD_human
HgenePENKC0027404Narcolepsy1CTD_human
HgenePENKC0027412Opioid-Related Disorders1CTD_human
HgenePENKC0027765nervous system disorder1CTD_human
HgenePENKC0029095Opioid abuse1CTD_human
HgenePENKC0030193Pain1CTD_human
HgenePENKC0033578Prostatic Neoplasms1CTD_human
HgenePENKC0234230Pain, Burning1CTD_human
HgenePENKC0234238Ache1CTD_human
HgenePENKC0234254Radiating pain1CTD_human
HgenePENKC0376358Malignant neoplasm of prostate1CTD_human
HgenePENKC0458257Pain, Splitting1CTD_human
HgenePENKC0458259Pain, Crushing1CTD_human
HgenePENKC0524661Narcotic Abuse1CTD_human
HgenePENKC0524662Opiate Addiction1CTD_human
HgenePENKC0751088Dyskinesia, Medication-Induced1CTD_human
HgenePENKC0751362Narcolepsy-Cataplexy Syndrome1CTD_human
HgenePENKC0751407Pain, Migratory1CTD_human
HgenePENKC0751408Suffering, Physical1CTD_human
HgenePENKC1527402Narcotic Dependence1CTD_human
HgenePENKC1862939AMYOTROPHIC LATERAL SCLEROSIS 11CTD_human
HgenePENKC1862941Amyotrophic Lateral Sclerosis, Sporadic1CTD_human
HgenePENKC4551628Opiate Abuse1CTD_human
HgenePENKC4551993Amyotrophic Lateral Sclerosis, Familial1CTD_human
TgeneCHGBC0036341Schizophrenia3PSYGENET
TgeneCHGBC0221765Chronic schizophrenia1PSYGENET