UTHEALTH HOME    ABOUT SBMI    A-Z    WEBMAIL    INSIDE THE UNIVERSITY
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine level1
leaf

Fusion Gene Summary

leaf

Fusion Gene Sample Information

leaf

Fusion ORF Analysis

leaf

Fusion Amino Acid Sequences

leaf

Fusion Protein Functional Features

leaf

Fusion Protein-Protein Interaction

leaf

Related drugs with this fusion protein

leaf

Related disease with this fusion protein

Fusion Protein:RMDN1-IMPA1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RMDN1-IMPA1
FusionPDB ID: 74236
FusionGDB2.0 ID: 74236
HgeneTgene
Gene symbol

RMDN1

IMPA1

Gene ID

51115

3612

Gene nameregulator of microtubule dynamics 1inositol monophosphatase 1
SynonymsCGI-90|FAM82B|RMD-1|RMD1IMP|IMPA|MRT59
Cytomap

8q21.3

8q21.13

Type of geneprotein-codingprotein-coding
Descriptionregulator of microtubule dynamics protein 1family with sequence similarity 82, member Bmicrotubule-associated proteininositol monophosphatase 1D-galactose 1-phosphate phosphataseIMP 1IMPase 1inositol(myo)-1(or 4)-monophosphatase 1inositol-1(or 4)-monophosphatase 1lithium-sensitive myo-inositol monophosphatase A1myo-inositol monophosphatase 1testicular tissue pro
Modification date2020031320200313
UniProtAcc

Q96DB5

P29218

Ensembl transtripts involved in fusion geneENST idsENST00000406452, ENST00000430676, 
ENST00000519966, ENST00000523911, 
ENST00000518772, 
ENST00000523710, 
ENST00000256108, ENST00000311489, 
ENST00000449740, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score5 X 6 X 2=602 X 3 X 2=12
# samples 62
** MAII scorelog2(6/60*10)=0log2(2/12*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: RMDN1 [Title/Abstract] AND IMPA1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RMDN1(87519223)-IMPA1(82572904), # samples:1
Anticipated loss of major functional domain due to fusion event.RMDN1-IMPA1 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.
RMDN1-IMPA1 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.
RMDN1-IMPA1 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.
RMDN1-IMPA1 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.
RMDN1-IMPA1 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
RMDN1-IMPA1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
RMDN1-IMPA1 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
TgeneIMPA1

GO:0046855

inositol phosphate dephosphorylation

9462881|17068342


check buttonFusion gene breakpoints across RMDN1 (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 IMPA1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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
ChiTaRS5.0N/ABM480140RMDN1chr8

87519223

-IMPA1chr8

82572904

-


Top

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)
ENST00000523911RMDN1chr887519223-ENST00000311489IMPA1chr882572904-79021510035484

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
ENST00000523911ENST00000311489RMDN1chr887519223-IMPA1chr882572904-0.120154770.8798452

Top

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

>74236_74236_1_RMDN1-IMPA1_RMDN1_chr8_87519223_ENST00000523911_IMPA1_chr8_82572904_ENST00000311489_length(amino acids)=84AA_BP=38

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

Top

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/chr8:87519223/chr8:82572904)
- 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
RMDN1

Q96DB5

IMPA1

P29218

FUNCTION: Responsible for the provision of inositol required for synthesis of phosphatidylinositol and polyphosphoinositides and has been implicated as the pharmacological target for lithium action in brain. Has broad substrate specificity and can use myo-inositol monophosphates, myo-inositol 1,3-diphosphate, myo-inositol 1,4-diphosphate, scyllo-inositol-phosphate, D-galactose 1-phosphate, glucose-1-phosphate, glucose-6-phosphate, fructose-1-phosphate, beta-glycerophosphate, and 2'-AMP as substrates. {ECO:0000269|PubMed:17068342, ECO:0000269|PubMed:8718889, ECO:0000269|PubMed:9462881}.

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
TgeneIMPA1chr8:87519223chr8:82572904ENST0000025610869194_196188.66666666666666278.0RegionSubstrate binding
TgeneIMPA1chr8:87519223chr8:82572904ENST0000031148958194_196152.33333333333334345.0RegionSubstrate binding

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRMDN1chr8:87519223chr8:82572904ENST00000406452-210168_20482.33333333333333315.0RepeatNote=TPR 1
HgeneRMDN1chr8:87519223chr8:82572904ENST00000406452-210222_25882.33333333333333315.0RepeatNote=TPR 2
TgeneIMPA1chr8:87519223chr8:82572904ENST000002561086992_95188.66666666666666278.0RegionSubstrate binding
TgeneIMPA1chr8:87519223chr8:82572904ENST000003114895892_95152.33333333333334345.0RegionSubstrate binding
TgeneIMPA1chr8:87519223chr8:82572904ENST00000449740710194_196247.66666666666666337.0RegionSubstrate binding
TgeneIMPA1chr8:87519223chr8:82572904ENST0000044974071092_95247.66666666666666337.0RegionSubstrate binding


Top

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
RMDN1
IMPA1


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


Top

Related Drugs to RMDN1-IMPA1


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

Top

Related Diseases to RMDN1-IMPA1


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