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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:INPP4B-MFSD11

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: INPP4B-MFSD11
FusionPDB ID: 39790
FusionGDB2.0 ID: 39790
HgeneTgene
Gene symbol

INPP4B

MFSD11

Gene ID

8821

79157

Gene nameinositol polyphosphate-4-phosphatase type II Bmajor facilitator superfamily domain containing 11
Synonyms-ET
Cytomap

4q31.21

17q25.1-q25.2

Type of geneprotein-codingprotein-coding
Descriptioninositol polyphosphate 4-phosphatase type IIinositol polyphosphate 4-phosphatase II; 4-phosphatase IIinositol polyphosphate-4-phosphatase, type II, 105kDatype II inositol 3,4-bisphosphate 4-phosphataseUNC93-like protein MFSD11major facilitator superfamily domain-containing protein 11protein ET
Modification date2020031320200313
UniProtAcc

O15327

O43934

Ensembl transtripts involved in fusion geneENST idsENST00000262992, ENST00000308502, 
ENST00000506217, ENST00000508116, 
ENST00000509777, ENST00000513000, 
ENST00000507861, ENST00000508084, 
ENST00000336509, ENST00000355954, 
ENST00000590070, ENST00000590393, 
ENST00000590514, ENST00000591864, 
ENST00000593181, ENST00000586622, 
ENST00000588460, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 12 X 5=7808 X 9 X 5=360
# samples 149
** MAII scorelog2(14/780*10)=-2.47804729680464
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/360*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: INPP4B [Title/Abstract] AND MFSD11 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)INPP4B(143324090)-MFSD11(74763467), # samples:1
Anticipated loss of major functional domain due to fusion event.INPP4B-MFSD11 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.
INPP4B-MFSD11 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.
INPP4B-MFSD11 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
INPP4B-MFSD11 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
INPP4B-MFSD11 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
INPP4B-MFSD11 seems lost the major protein functional domain in Hgene 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 INPP4B (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 MFSD11 (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
ChimerDB4SKCMTCGA-D3-A2J7INPP4Bchr4

143324090

-MFSD11chr17

74763467

+


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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)
ENST00000262992INPP4Bchr4143324090-ENST00000586622MFSD11chr1774763467+17225896211256211
ENST00000262992INPP4Bchr4143324090-ENST00000588460MFSD11chr1774763467+14775896211256211

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
ENST00000262992ENST00000586622INPP4Bchr4143324090-MFSD11chr1774763467+0.0050478630.9949522
ENST00000262992ENST00000588460INPP4Bchr4143324090-MFSD11chr1774763467+0.0071886370.9928114

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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

>39790_39790_1_INPP4B-MFSD11_INPP4B_chr4_143324090_ENST00000262992_MFSD11_chr17_74763467_ENST00000586622_length(amino acids)=211AA_BP=
MLLLSITTAYTGLELTFFSGVYGTCIGATNKFGAEEKSLIGLSGIFIGIGEILGGSLFGLLSKNNRFGRNPVVLLGILVHFIAFYLIFLN
MPGDAPIAPVKGTDSSAYIKSSKEVAILCSFLLGLGDSCFNTQLLSILGFLYSEDSAPAFAIFKFVQSICAAVAFFYSNYLLLHWQLLVM

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

>39790_39790_2_INPP4B-MFSD11_INPP4B_chr4_143324090_ENST00000262992_MFSD11_chr17_74763467_ENST00000588460_length(amino acids)=211AA_BP=
MLLLSITTAYTGLELTFFSGVYGTCIGATNKFGAEEKSLIGLSGIFIGIGEILGGSLFGLLSKNNRFGRNPVVLLGILVHFIAFYLIFLN
MPGDAPIAPVKGTDSSAYIKSSKEVAILCSFLLGLGDSCFNTQLLSILGFLYSEDSAPAFAIFKFVQSICAAVAFFYSNYLLLHWQLLVM

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

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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/chr4:143324090/chr17:74763467)
- 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
INPP4B

O15327

MFSD11

O43934

FUNCTION: Catalyzes the hydrolysis of the 4-position phosphate of phosphatidylinositol 3,4-bisphosphate, inositol 1,3,4-trisphosphate and inositol 3,4-trisphosphate (PubMed:24070612, PubMed:24591580). Plays a role in the late stages of macropinocytosis by dephosphorylating phosphatidylinositol 3,4-bisphosphate in membrane ruffles (PubMed:24591580). The lipid phosphatase activity is critical for tumor suppressor function. Antagonizes the PI3K-AKT/PKB signaling pathway by dephosphorylating phosphoinositides and thereby modulating cell cycle progression and cell survival (PubMed:19647222, PubMed:24070612). {ECO:0000269|PubMed:19647222, ECO:0000269|PubMed:24070612, ECO:0000269|PubMed:24591580}.

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
TgeneMFSD11chr4:143324090chr17:74763467ENST00000336509814239_259227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000336509814277_297227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000336509814309_329227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000336509814359_379227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000336509814385_405227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000336509814410_430227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000355954612239_259175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000355954612277_297175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000355954612309_329175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000355954612359_379175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000355954612385_405175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000355954612410_430175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000586622915239_259227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000586622915277_297227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000586622915309_329227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000586622915359_379227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000586622915385_405227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000586622915410_430227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000588460713239_259227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000588460713277_297227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000588460713309_329227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000588460713359_379227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000588460713385_405227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000588460713410_430227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000590514814239_259227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000590514814277_297227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000590514814309_329227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000590514814359_379227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000590514814385_405227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000590514814410_430227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000593181612239_259175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000593181612277_297175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000593181612309_329175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000593181612359_379175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000593181612385_405175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000593181612410_430175.33333333333334398.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneINPP4Bchr4:143324090chr17:74763467ENST00000262992-52423_165124.0925.0DomainC2
HgeneINPP4Bchr4:143324090chr17:74763467ENST00000308502-42323_165124.0925.0DomainC2
HgeneINPP4Bchr4:143324090chr17:74763467ENST00000506217-4523_165124.0132.0DomainC2
HgeneINPP4Bchr4:143324090chr17:74763467ENST00000508116-62523_165124.0925.0DomainC2
HgeneINPP4Bchr4:143324090chr17:74763467ENST00000513000-82723_165124.0925.0DomainC2
TgeneMFSD11chr4:143324090chr17:74763467ENST00000336509814138_158227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000336509814170_190227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000033650981453_73227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000033650981474_94227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST000003365098148_28227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000033650981496_116227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000355954612138_158175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000355954612170_190175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000035595461253_73175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000035595461274_94175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST000003559546128_28175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000035595461296_116175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000586622915138_158227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000586622915170_190227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000058662291553_73227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000058662291574_94227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST000005866229158_28227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000058662291596_116227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000588460713138_158227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000588460713170_190227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000058846071353_73227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000058846071374_94227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST000005884607138_28227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000058846071396_116227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000590514814138_158227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000590514814170_190227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000059051481453_73227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000059051481474_94227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST000005905148148_28227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000059051481496_116227.33333333333334450.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000593181612138_158175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST00000593181612170_190175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000059318161253_73175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000059318161274_94175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST000005931816128_28175.33333333333334398.0TransmembraneHelical
TgeneMFSD11chr4:143324090chr17:74763467ENST0000059318161296_116175.33333333333334398.0TransmembraneHelical


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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
INPP4B
MFSD11


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 INPP4B-MFSD11


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 INPP4B-MFSD11


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