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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:PPM1H-WIF1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: PPM1H-WIF1
FusionPDB ID: 67669
FusionGDB2.0 ID: 67669
HgeneTgene
Gene symbol

PPM1H

WIF1

Gene ID

57460

11197

Gene nameprotein phosphatase, Mg2+/Mn2+ dependent 1HWNT inhibitory factor 1
SynonymsARHCL1|NERPP-2C|URCC2WIF-1
Cytomap

12q14.1-q14.2

12q14.3

Type of geneprotein-codingprotein-coding
Descriptionprotein phosphatase 1Hneurite extension-related protein phosphatase related to PP2Cprotein phosphatase 1H (PP2C domain containing)ras homolog gene family, member C like 1wnt inhibitory factor 1
Modification date2020032720200313
UniProtAcc.

Q9Y5W5

Ensembl transtripts involved in fusion geneENST idsENST00000551214, ENST00000228705, 
ENST00000286574, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score23 X 21 X 11=53137 X 11 X 6=462
# samples 2914
** MAII scorelog2(29/5313*10)=-4.19540190745814
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/462*10)=-1.72246602447109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: PPM1H [Title/Abstract] AND WIF1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)PPM1H(63131282)-WIF1(65462684), # samples:3
Anticipated loss of major functional domain due to fusion event.PPM1H-WIF1 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.
PPM1H-WIF1 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.
PPM1H-WIF1 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.
PPM1H-WIF1 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.
PPM1H-WIF1 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
PPM1H-WIF1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
PPM1H-WIF1 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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

check buttonFusion gene breakpoints across PPM1H (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 WIF1 (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
ChimerDB4ESCATCGA-L5-A43MPPM1Hchr12

63087715

-WIF1chr12

65471634

-
ChimerDB4PRADTCGA-XJ-A9DX-01APPM1Hchr12

63131282

-WIF1chr12

65462684

-
ChimerDB4PRADTCGA-XJ-A9DXPPM1Hchr12

63131282

-WIF1chr12

65462684

-


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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)
ENST00000228705PPM1Hchr1263087715-ENST00000286574WIF1chr1265471634-301314381602289709

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
ENST00000228705ENST00000286574PPM1Hchr1263087715-WIF1chr1265471634-0.0063880970.9936119

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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

>67669_67669_1_PPM1H-WIF1_PPM1H_chr12_63087715_ENST00000228705_WIF1_chr12_65471634_ENST00000286574_length(amino acids)=709AA_BP=426
MGAARGASQWPDSPCARRPPQPACPALRLARPPPPPARTAAAGRRSNMLTRVKSAVANFMGGIMAGSSGSEHGGGSCGGSDLPLRFPYGR
PEFLGLSQDEVECSADHIARPILILKETRRLPWATGYAEVINAGKSTHNEDQASCEVLTVKKKAGAVTSTPNRNSSKRRSSLPNGEGLQL
KENSESEGVSCHYWSLFDGHAGSGAAVVASRLLQHHITEQLQDIVDILKNSAVLPPTCLGEEPENTPANSRTLTRAASLRGGVGAPGSPS
TPPTRFFTEKKIPHECLVIGALESAFKEMDLQIERERSSYNISGGCTALIVICLLGKLYVANAGDSRAIIIRNGEIIPMSSEFTPETERQ
RLQYLAFMQPHLLGNEFTHLEFPRRVQRKELGKKMLYRDFNMTGWAYKTIEDEDLKFPLIYGEGKKAEYFYEFLSLRSLDKGIMADPTVN
VPLLGTVPHKASVVQVGFPCLGKQDGVAAFEVDVIVMNSEGNTILQTPQNAIFFKTCQQAECPGGCRNGGFCNERRICECPDGFHGPHCE
KALCTPRCMNGGLCVTPGFCICPPGFYGVNCDKANCSTTCFNGGTCFYPGKCICPPGLEGEQCEISKCPQPCRNGGKCIGKSKCKCSKGY

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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/chr12:63131282/chr12:65462684)
- 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
.WIF1

Q9Y5W5

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: Binds to WNT proteins and inhibits their activities. May be involved in mesoderm segmentation.

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
TgeneWIF1chr12:63087715chr12:65471634ENST00000286574110178_21096.0380.0DomainEGF-like 1
TgeneWIF1chr12:63087715chr12:65471634ENST00000286574110211_24296.0380.0DomainEGF-like 2
TgeneWIF1chr12:63087715chr12:65471634ENST00000286574110243_27196.0380.0DomainEGF-like 3
TgeneWIF1chr12:63087715chr12:65471634ENST00000286574110274_30696.0380.0DomainEGF-like 4
TgeneWIF1chr12:63087715chr12:65471634ENST00000286574110307_33896.0380.0DomainEGF-like 5

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgenePPM1Hchr12:63087715chr12:65471634ENST00000228705-71077_507379.0515.0DomainPPM-type phosphatase
TgeneWIF1chr12:63087715chr12:65471634ENST0000028657411038_17796.0380.0DomainWIF


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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
PPM1H
WIF1all structure


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


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Related Drugs to PPM1H-WIF1


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 PPM1H-WIF1


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
TgeneWIF1C0009402Colorectal Carcinoma1CTD_human
TgeneWIF1C0009404Colorectal Neoplasms1CTD_human
TgeneWIF1C0014859Esophageal Neoplasms1CTD_human
TgeneWIF1C0024623Malignant neoplasm of stomach1CTD_human
TgeneWIF1C0027439Nasopharyngeal Neoplasms1CTD_human
TgeneWIF1C0038356Stomach Neoplasms1CTD_human
TgeneWIF1C0238301Cancer of Nasopharynx1CTD_human
TgeneWIF1C0546837Malignant neoplasm of esophagus1CTD_human
TgeneWIF1C1708349Hereditary Diffuse Gastric Cancer1CTD_human