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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:MGLL-RNF13

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MGLL-RNF13
FusionPDB ID: 53401
FusionGDB2.0 ID: 53401
HgeneTgene
Gene symbol

MGLL

RNF13

Gene ID

11343

11342

Gene namemonoglyceride lipasering finger protein 13
SynonymsHU-K5|HUK5|MAGL|MGLEIEE73|RZF
Cytomap

3q21.3

3q25.1

Type of geneprotein-codingprotein-coding
Descriptionmonoglyceride lipaselysophospholipase homologmonoacylglycerol lipaseE3 ubiquitin-protein ligase RNF13RING zinc finger proteinRING-type E3 ubiquitin transferase RNF13
Modification date2020031320200313
UniProtAcc

Q99685

Q8WVD3

Ensembl transtripts involved in fusion geneENST idsENST00000434178, ENST00000265052, 
ENST00000398104, ENST00000453507, 
ENST00000398101, ENST00000476682, 
ENST00000344229, ENST00000361785, 
ENST00000392894, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 7 X 4=19617 X 12 X 8=1632
# samples 817
** MAII scorelog2(8/196*10)=-1.29278174922785
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(17/1632*10)=-3.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: MGLL [Title/Abstract] AND RNF13 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MGLL(127500632)-RNF13(149677843), # samples:1
Anticipated loss of major functional domain due to fusion event.MGLL-RNF13 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.
MGLL-RNF13 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.
MGLL-RNF13 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.
MGLL-RNF13 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.
MGLL-RNF13 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
MGLL-RNF13 seems lost the major protein functional domain in Hgene 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
HgeneMGLL

GO:0046464

acylglycerol catabolic process

22969151


check buttonFusion gene breakpoints across MGLL (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 RNF13 (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
ChimerDB4STADTCGA-CD-8534-01AMGLLchr3

127500632

-RNF13chr3

149677843

+


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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)
ENST00000265052MGLLchr3127500632-ENST00000392894RNF13chr3149677843+22838024861247253
ENST00000265052MGLLchr3127500632-ENST00000344229RNF13chr3149677843+22668024861247253
ENST00000265052MGLLchr3127500632-ENST00000361785RNF13chr3149677843+22708024861247253
ENST00000398104MGLLchr3127500632-ENST00000392894RNF13chr3149677843+185837761822253
ENST00000398104MGLLchr3127500632-ENST00000344229RNF13chr3149677843+184137761822253
ENST00000398104MGLLchr3127500632-ENST00000361785RNF13chr3149677843+184537761822253
ENST00000453507MGLLchr3127500632-ENST00000392894RNF13chr3149677843+177629533740235
ENST00000453507MGLLchr3127500632-ENST00000344229RNF13chr3149677843+175929533740235
ENST00000453507MGLLchr3127500632-ENST00000361785RNF13chr3149677843+176329533740235

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
ENST00000265052ENST00000392894MGLLchr3127500632-RNF13chr3149677843+0.0010905340.9989095
ENST00000265052ENST00000344229MGLLchr3127500632-RNF13chr3149677843+0.0011269110.99887305
ENST00000265052ENST00000361785MGLLchr3127500632-RNF13chr3149677843+0.0011064130.99889356
ENST00000398104ENST00000392894MGLLchr3127500632-RNF13chr3149677843+0.0011183370.99888164
ENST00000398104ENST00000344229MGLLchr3127500632-RNF13chr3149677843+0.0011704880.99882954
ENST00000398104ENST00000361785MGLLchr3127500632-RNF13chr3149677843+0.0011587910.9988412
ENST00000453507ENST00000392894MGLLchr3127500632-RNF13chr3149677843+0.0006666340.9993333
ENST00000453507ENST00000344229MGLLchr3127500632-RNF13chr3149677843+0.0006486710.9993513
ENST00000453507ENST00000361785MGLLchr3127500632-RNF13chr3149677843+0.000649270.9993507

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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

>53401_53401_1_MGLL-RNF13_MGLL_chr3_127500632_ENST00000265052_RNF13_chr3_149677843_ENST00000344229_length(amino acids)=253AA_BP=105
MVLILQAVVVVECKRQHIMETGPEDPSSMPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEELA
RMLMGLDLLVFAHDHGDEYDVCAICLDEYEDGDKLRILPCSHAYHCKCVDPWLTKTKKTCPVCKQKVVPSQGDSDSDTDSSQEENEVTEH

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

>53401_53401_2_MGLL-RNF13_MGLL_chr3_127500632_ENST00000265052_RNF13_chr3_149677843_ENST00000361785_length(amino acids)=253AA_BP=105
MVLILQAVVVVECKRQHIMETGPEDPSSMPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEELA
RMLMGLDLLVFAHDHGDEYDVCAICLDEYEDGDKLRILPCSHAYHCKCVDPWLTKTKKTCPVCKQKVVPSQGDSDSDTDSSQEENEVTEH

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

>53401_53401_3_MGLL-RNF13_MGLL_chr3_127500632_ENST00000265052_RNF13_chr3_149677843_ENST00000392894_length(amino acids)=253AA_BP=105
MVLILQAVVVVECKRQHIMETGPEDPSSMPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEELA
RMLMGLDLLVFAHDHGDEYDVCAICLDEYEDGDKLRILPCSHAYHCKCVDPWLTKTKKTCPVCKQKVVPSQGDSDSDTDSSQEENEVTEH

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

>53401_53401_4_MGLL-RNF13_MGLL_chr3_127500632_ENST00000398104_RNF13_chr3_149677843_ENST00000344229_length(amino acids)=253AA_BP=105
MARRKRGSAALGERDSGARGPGPEDPSSMPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEELA
RMLMGLDLLVFAHDHGDEYDVCAICLDEYEDGDKLRILPCSHAYHCKCVDPWLTKTKKTCPVCKQKVVPSQGDSDSDTDSSQEENEVTEH

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

>53401_53401_5_MGLL-RNF13_MGLL_chr3_127500632_ENST00000398104_RNF13_chr3_149677843_ENST00000361785_length(amino acids)=253AA_BP=105
MARRKRGSAALGERDSGARGPGPEDPSSMPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEELA
RMLMGLDLLVFAHDHGDEYDVCAICLDEYEDGDKLRILPCSHAYHCKCVDPWLTKTKKTCPVCKQKVVPSQGDSDSDTDSSQEENEVTEH

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

>53401_53401_6_MGLL-RNF13_MGLL_chr3_127500632_ENST00000398104_RNF13_chr3_149677843_ENST00000392894_length(amino acids)=253AA_BP=105
MARRKRGSAALGERDSGARGPGPEDPSSMPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEELA
RMLMGLDLLVFAHDHGDEYDVCAICLDEYEDGDKLRILPCSHAYHCKCVDPWLTKTKKTCPVCKQKVVPSQGDSDSDTDSSQEENEVTEH

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

>53401_53401_7_MGLL-RNF13_MGLL_chr3_127500632_ENST00000453507_RNF13_chr3_149677843_ENST00000344229_length(amino acids)=235AA_BP=87
METGPEDPSSMPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEELARMLMGLDLLVFAHDHGDE
YDVCAICLDEYEDGDKLRILPCSHAYHCKCVDPWLTKTKKTCPVCKQKVVPSQGDSDSDTDSSQEENEVTEHTPLLRPLASVSAQSFGAL

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

>53401_53401_8_MGLL-RNF13_MGLL_chr3_127500632_ENST00000453507_RNF13_chr3_149677843_ENST00000361785_length(amino acids)=235AA_BP=87
METGPEDPSSMPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEELARMLMGLDLLVFAHDHGDE
YDVCAICLDEYEDGDKLRILPCSHAYHCKCVDPWLTKTKKTCPVCKQKVVPSQGDSDSDTDSSQEENEVTEHTPLLRPLASVSAQSFGAL

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

>53401_53401_9_MGLL-RNF13_MGLL_chr3_127500632_ENST00000453507_RNF13_chr3_149677843_ENST00000392894_length(amino acids)=235AA_BP=87
METGPEDPSSMPEESSPRRTPQSIPYQDLPHLVNADGQYLFCRYWKPTGTPKALIFVSHGAGEHSGRYEELARMLMGLDLLVFAHDHGDE
YDVCAICLDEYEDGDKLRILPCSHAYHCKCVDPWLTKTKKTCPVCKQKVVPSQGDSDSDTDSSQEENEVTEHTPLLRPLASVSAQSFGAL

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

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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/chr3:127500632/chr3:149677843)
- 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
MGLL

Q99685

RNF13

Q8WVD3

FUNCTION: Converts monoacylglycerides to free fatty acids and glycerol (PubMed:19029917, PubMed:20079333, PubMed:21049984, PubMed:22969151, PubMed:24368842). Hydrolyzes the endocannabinoid 2-arachidonoylglycerol, and thereby contributes to the regulation of endocannabinoid signaling, nociperception and perception of pain (PubMed:19029917, PubMed:20079333, PubMed:21049984, PubMed:22969151, PubMed:24368842). Regulates the levels of fatty acids that serve as signaling molecules and promote cancer cell migration, invasion and tumor growth (PubMed:20079333). {ECO:0000269|PubMed:19029917, ECO:0000269|PubMed:20079333, ECO:0000269|PubMed:21049984, ECO:0000269|PubMed:22969151, ECO:0000269|PubMed:24368842}.FUNCTION: E3 ubiquitin-protein ligase involved in DNA damage response by promoting DNA resection and homologous recombination (PubMed:26502055, PubMed:26502057). Recruited to sites of double-strand breaks following DNA damage and specifically promotes double-strand break repair via homologous recombination (PubMed:26502055, PubMed:26502057). Two different, non-exclusive, mechanisms have been proposed. According to a report, regulates the choice of double-strand break repair by favoring homologous recombination over non-homologous end joining (NHEJ): acts by mediating ubiquitination of XRCC5/Ku80, leading to remove the Ku complex from DNA breaks, thereby promoting homologous recombination (PubMed:26502055). According to another report, cooperates with UBE2Ds E2 ubiquitin ligases (UBE2D1, UBE2D2, UBE2D3 or UBE2D4) to promote homologous recombination by mediating ubiquitination of RBBP8/CtIP (PubMed:26502057). Together with NLK, involved in the ubiquitination and degradation of TCF/LEF (PubMed:16714285). Also exhibits auto-ubiquitination activity in combination with UBE2K (PubMed:16714285). May act as a negative regulator in the Wnt/beta-catenin-mediated signaling pathway (PubMed:16714285). {ECO:0000269|PubMed:16714285, ECO:0000269|PubMed:26502055, ECO:0000269|PubMed:26502057}.

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
TgeneRNF13chr3:127500632chr3:149677843ENST00000344229811240_282233.33333333333334382.0Zinc fingerRING-type%3B atypical
TgeneRNF13chr3:127500632chr3:149677843ENST00000392894710240_282233.33333333333334382.0Zinc fingerRING-type%3B atypical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneRNF13chr3:127500632chr3:149677843ENST0000034422981165_160233.33333333333334382.0DomainNote=PA
TgeneRNF13chr3:127500632chr3:149677843ENST0000039289471065_160233.33333333333334382.0DomainNote=PA
TgeneRNF13chr3:127500632chr3:149677843ENST00000344229811204_381233.33333333333334382.0Topological domainCytoplasmic
TgeneRNF13chr3:127500632chr3:149677843ENST0000034422981135_182233.33333333333334382.0Topological domainLumenal
TgeneRNF13chr3:127500632chr3:149677843ENST00000392894710204_381233.33333333333334382.0Topological domainCytoplasmic
TgeneRNF13chr3:127500632chr3:149677843ENST0000039289471035_182233.33333333333334382.0Topological domainLumenal
TgeneRNF13chr3:127500632chr3:149677843ENST00000344229811183_203233.33333333333334382.0TransmembraneHelical
TgeneRNF13chr3:127500632chr3:149677843ENST00000392894710183_203233.33333333333334382.0TransmembraneHelical


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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
MGLL
RNF13


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 MGLL-RNF13


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 MGLL-RNF13


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