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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:MTMR12-GEMIN4 (FusionGDB2 ID:55408)

Fusion Gene Summary for MTMR12-GEMIN4

check button Fusion gene summary
Fusion gene informationFusion gene name: MTMR12-GEMIN4
Fusion gene ID: 55408
HgeneTgene
Gene symbol

MTMR12

GEMIN4

Gene ID

54545

50628

Gene namemyotubularin related protein 12gem nuclear organelle associated protein 4
Synonyms3-PAP|PIP3APHC56|HCAP1|HHRF-1|NEDMCR|p97
Cytomap

5p13.3

17p13.3

Type of geneprotein-codingprotein-coding
Descriptionmyotubularin-related protein 123-phosphatase adapter protein3-phosphatase adapter subunitinactive phosphatidylinositol 3-phosphatase 12phosphatidylinositol 3 phosphate 3-phosphatase adapter subunitphosphatidylinositol-3 phosphate 3-phosphatase adaptogem-associated protein 4HCC-associated protein 1component of gems 4gemin-4
Modification date2020031320200313
UniProtAcc

Q9C0I1

P57678

Ensembl transtripts involved in fusion geneENST00000280285, ENST00000382142, 
ENST00000264934, ENST00000510216, 
ENST00000319004, ENST00000437269, 
ENST00000576778, 
Fusion gene scores* DoF score12 X 11 X 10=13204 X 1 X 3=12
# samples 154
** MAII scorelog2(15/1320*10)=-3.13750352374993
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/12*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MTMR12 [Title/Abstract] AND GEMIN4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointMTMR12(32312863)-GEMIN4(651272), # samples:1
Anticipated loss of major functional domain due to fusion event.MTMR12-GEMIN4 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
MTMR12-GEMIN4 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
MTMR12-GEMIN4 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
TgeneGEMIN4

GO:0000387

spliceosomal snRNP assembly

18984161


check buttonFusion gene breakpoints across MTMR12 (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 GEMIN4 (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
ChimerDB4Non-Cancer5357NMTMR12chr5

32312863

-GEMIN4chr17

651272

-


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Fusion Gene ORF analysis for MTMR12-GEMIN4

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
Frame-shiftENST00000280285ENST00000319004MTMR12chr5

32312863

-GEMIN4chr17

651272

-
Frame-shiftENST00000280285ENST00000437269MTMR12chr5

32312863

-GEMIN4chr17

651272

-
5CDS-5UTRENST00000280285ENST00000576778MTMR12chr5

32312863

-GEMIN4chr17

651272

-
Frame-shiftENST00000382142ENST00000319004MTMR12chr5

32312863

-GEMIN4chr17

651272

-
Frame-shiftENST00000382142ENST00000437269MTMR12chr5

32312863

-GEMIN4chr17

651272

-
5CDS-5UTRENST00000382142ENST00000576778MTMR12chr5

32312863

-GEMIN4chr17

651272

-
Frame-shiftENST00000264934ENST00000319004MTMR12chr5

32312863

-GEMIN4chr17

651272

-
Frame-shiftENST00000264934ENST00000437269MTMR12chr5

32312863

-GEMIN4chr17

651272

-
5CDS-5UTRENST00000264934ENST00000576778MTMR12chr5

32312863

-GEMIN4chr17

651272

-
intron-3CDSENST00000510216ENST00000319004MTMR12chr5

32312863

-GEMIN4chr17

651272

-
intron-3CDSENST00000510216ENST00000437269MTMR12chr5

32312863

-GEMIN4chr17

651272

-
intron-5UTRENST00000510216ENST00000576778MTMR12chr5

32312863

-GEMIN4chr17

651272

-

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 MTMR12-GEMIN4


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 MTMR12-GEMIN4


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
MTMR12

Q9C0I1

GEMIN4

P57678

FUNCTION: Acts as an adapter for the myotubularin-related phosphatases (PubMed:11504939, PubMed:12847286, PubMed:23818870). Regulates phosphatase MTM1 protein stability and possibly its intracellular location (PubMed:23818870). By stabilizing MTM1 protein levels, required for skeletal muscle maintenance but not for myogenesis (By similarity). {ECO:0000250|UniProtKB:Q80TA6, ECO:0000269|PubMed:11504939, ECO:0000269|PubMed:12847286, ECO:0000269|PubMed:23818870}.FUNCTION: The SMN complex plays a catalyst role in the assembly of small nuclear ribonucleoproteins (snRNPs), the building blocks of the spliceosome. Thereby, plays an important role in the splicing of cellular pre-mRNAs. Most spliceosomal snRNPs contain a common set of Sm proteins SNRPB, SNRPD1, SNRPD2, SNRPD3, SNRPE, SNRPF and SNRPG that assemble in a heptameric protein ring on the Sm site of the small nuclear RNA to form the core snRNP. In the cytosol, the Sm proteins SNRPD1, SNRPD2, SNRPE, SNRPF and SNRPG are trapped in an inactive 6S pICln-Sm complex by the chaperone CLNS1A that controls the assembly of the core snRNP. Dissociation by the SMN complex of CLNS1A from the trapped Sm proteins and their transfer to an SMN-Sm complex triggers the assembly of core snRNPs and their transport to the nucleus. {ECO:0000269|PubMed:18984161}.

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 MTMR12-GEMIN4


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 MTMR12-GEMIN4


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 MTMR12-GEMIN4


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 MTMR12-GEMIN4


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneGEMIN4C4693567NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES3GENOMICS_ENGLAND;UNIPROT
TgeneGEMIN4C0001973Alcoholic Intoxication, Chronic1PSYGENET