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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:ZNHIT1-PPP1R1B

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ZNHIT1-PPP1R1B
FusionPDB ID: 103131
FusionGDB2.0 ID: 103131
HgeneTgene
Gene symbol

ZNHIT1

PPP1R1B

Gene ID

10467

84152

Gene namezinc finger HIT-type containing 1protein phosphatase 1 regulatory inhibitor subunit 1B
SynonymsCG1I|ZNFN4A1DARPP-32|DARPP32
Cytomap

7q22.1

17q12

Type of geneprotein-codingprotein-coding
Descriptionzinc finger HIT domain-containing protein 1H_DJ0747G18.14cyclin-G1-binding protein 1p18 Hamletp18Hamletputative cyclin G1 interacting proteinzinc finger protein subfamily 4A member 1zinc finger protein, subfamily 4A (HIT domain containing), member protein phosphatase 1 regulatory subunit 1Bdopamine and cAMP-regulated neuronal phosphoprotein 32
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST idsENST00000492315, ENST00000305105, 
ENST00000254079, ENST00000394265, 
ENST00000394267, ENST00000579000, 
ENST00000580825, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 3 X 2=1817 X 10 X 9=1530
# samples 326
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(26/1530*10)=-2.55694812455156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: ZNHIT1 [Title/Abstract] AND PPP1R1B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ZNHIT1(100861498)-PPP1R1B(37791860), # samples:3
Anticipated loss of major functional domain due to fusion event.ZNHIT1-PPP1R1B seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
ZNHIT1-PPP1R1B seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
ZNHIT1-PPP1R1B seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
ZNHIT1-PPP1R1B seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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
TgenePPP1R1B

GO:0032515

negative regulation of phosphoprotein phosphatase activity

10807923


check buttonFusion gene breakpoints across ZNHIT1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across PPP1R1B (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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-E2-A1LE-01AZNHIT1chr7

100861498

-PPP1R1Bchr17

37791860

+
ChimerDB4BRCATCGA-E2-A1LE-01AZNHIT1chr7

100861498

+PPP1R1Bchr17

37791860

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000305105ZNHIT1chr7100861498+ENST00000580825PPP1R1Bchr1737791860+8555504422147
ENST00000305105ZNHIT1chr7100861498+ENST00000254079PPP1R1Bchr1737791860+14815506731131152
ENST00000305105ZNHIT1chr7100861498+ENST00000579000PPP1R1Bchr1737791860+14775506731131152
ENST00000305105ZNHIT1chr7100861498+ENST00000394265PPP1R1Bchr1737791860+14805506731131152
ENST00000305105ZNHIT1chr7100861498+ENST00000394267PPP1R1Bchr1737791860+14815506731131152

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
ENST00000305105ENST00000580825ZNHIT1chr7100861498+PPP1R1Bchr1737791860+0.87179680.12820318
ENST00000305105ENST00000254079ZNHIT1chr7100861498+PPP1R1Bchr1737791860+0.863344130.13665585
ENST00000305105ENST00000579000ZNHIT1chr7100861498+PPP1R1Bchr1737791860+0.85042760.14957231
ENST00000305105ENST00000394265ZNHIT1chr7100861498+PPP1R1Bchr1737791860+0.85956220.14043777
ENST00000305105ENST00000394267ZNHIT1chr7100861498+PPP1R1Bchr1737791860+0.863344130.13665585

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>103131_103131_1_ZNHIT1-PPP1R1B_ZNHIT1_chr7_100861498_ENST00000305105_PPP1R1B_chr17_37791860_ENST00000254079_length(amino acids)=152AA_BP=
MGRNLSALPPLSLAHRHPACISQEEVEGTSLFPRNPLYPHPVLCSSPRLLGLRLLTSRRLRLVCVCLFAHLWLIPREPGHLLPDAHPCQS

--------------------------------------------------------------

>103131_103131_2_ZNHIT1-PPP1R1B_ZNHIT1_chr7_100861498_ENST00000305105_PPP1R1B_chr17_37791860_ENST00000394265_length(amino acids)=152AA_BP=
MGRNLSALPPLSLAHRHPACISQEEVEGTSLFPRNPLYPHPVLCSSPRLLGLRLLTSRRLRLVCVCLFAHLWLIPREPGHLLPDAHPCQS

--------------------------------------------------------------

>103131_103131_3_ZNHIT1-PPP1R1B_ZNHIT1_chr7_100861498_ENST00000305105_PPP1R1B_chr17_37791860_ENST00000394267_length(amino acids)=152AA_BP=
MGRNLSALPPLSLAHRHPACISQEEVEGTSLFPRNPLYPHPVLCSSPRLLGLRLLTSRRLRLVCVCLFAHLWLIPREPGHLLPDAHPCQS

--------------------------------------------------------------

>103131_103131_4_ZNHIT1-PPP1R1B_ZNHIT1_chr7_100861498_ENST00000305105_PPP1R1B_chr17_37791860_ENST00000579000_length(amino acids)=152AA_BP=
MGRNLSALPPLSLAHRHPACISQEEVEGTSLFPRNPLYPHPVLCSSPRLLGLRLLTSRRLRLVCVCLFAHLWLIPREPGHLLPDAHPCQS

--------------------------------------------------------------

>103131_103131_5_ZNHIT1-PPP1R1B_ZNHIT1_chr7_100861498_ENST00000305105_PPP1R1B_chr17_37791860_ENST00000580825_length(amino acids)=147AA_BP=
MYFCACATALTHYVAFPWRQESFSPCFIGAKPLPASVWRCKSCGSHEMGHFKDVVTVFLQEILFSFGPCEDAVITKAAPGASPGRRGGGL

--------------------------------------------------------------

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Fusion Protein Functional Features


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/chr7:100861498/chr17:37791860)
- 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
..
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: 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.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgenePPP1R1Bchr7:100861498chr17:37791860ENST0000039426547119_136112.33333333333333169.0Compositional biasNote=Asp/Glu-rich (acidic)
TgenePPP1R1Bchr7:100861498chr17:37791860ENST0000039426747119_136112.33333333333333169.0Compositional biasNote=Asp/Glu-rich (acidic)

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneZNHIT1chr7:100861498chr17:37791860ENST00000305105+1523_397.333333333333333155.0Coiled coilOntology_term=ECO:0000255
HgeneZNHIT1chr7:100861498chr17:37791860ENST00000305105+1566_707.333333333333333155.0Compositional biasNote=Poly-Lys
HgeneZNHIT1chr7:100861498chr17:37791860ENST00000305105+1538_477.333333333333333155.0MotifNuclear localization signal
HgeneZNHIT1chr7:100861498chr17:37791860ENST00000305105+15117_1497.333333333333333155.0Zinc fingerHIT-type
TgenePPP1R1Bchr7:100861498chr17:37791860ENST0000025407947119_136148.33333333333334205.0Compositional biasNote=Asp/Glu-rich (acidic)
TgenePPP1R1Bchr7:100861498chr17:37791860ENST0000058082558119_136148.33333333333334205.0Compositional biasNote=Asp/Glu-rich (acidic)


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
ZNHIT1
PPP1R1B


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
HgeneZNHIT1chr7:100861498chr17:37791860ENST00000305105+1572_1107.333333333333333155.0NR1D2


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Related Drugs to ZNHIT1-PPP1R1B


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to ZNHIT1-PPP1R1B


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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