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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:TRERF1-GNMT (FusionGDB2 ID:93284)

Fusion Gene Summary for TRERF1-GNMT

check button Fusion gene summary
Fusion gene informationFusion gene name: TRERF1-GNMT
Fusion gene ID: 93284
HgeneTgene
Gene symbol

TRERF1

GNMT

Gene ID

55809

27232

Gene nametranscriptional regulating factor 1glycine N-methyltransferase
SynonymsBCAR2|HSA277276|RAPA|TREP132|TReP-132|dJ139D8.5HEL-S-182mP
Cytomap

6p21.1

6p21.1

Type of geneprotein-codingprotein-coding
Descriptiontranscriptional-regulating factor 1breast cancer anti-estrogen resistance 2rapa-1rapa-2transcriptional regulating protein 132zinc finger protein rapazinc finger transcription factor TReP-132glycine N-methyltransferaseepididymis secretory sperm binding protein Li 182mP
Modification date2020031320200313
UniProtAcc.

Q14749

Ensembl transtripts involved in fusion geneENST00000541110, ENST00000372917, 
ENST00000372922, ENST00000340840, 
ENST00000354325, 
ENST00000372808, 
Fusion gene scores* DoF score15 X 11 X 7=11554 X 3 X 4=48
# samples 164
** MAII scorelog2(16/1155*10)=-2.85174904141606
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/48*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TRERF1 [Title/Abstract] AND GNMT [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTRERF1(42330735)-GNMT(42929950), # samples:1
TRERF1(42330685)-GNMT(42929950), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneTRERF1

GO:0045893

positive regulation of transcription, DNA-templated

11349124

TgeneGNMT

GO:0046500

S-adenosylmethionine metabolic process

15340920


check buttonFusion gene breakpoints across TRERF1 (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 GNMT (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
ChimerDB4LUADTCGA-50-6591-01ATRERF1chr6

42330735

-GNMTchr6

42929950

+
ChimerDB4LUADTCGA-50-6591-01ATRERF1chr6

42330685

-GNMTchr6

42929950

+


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Fusion Gene ORF analysis for TRERF1-GNMT

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
5UTR-3CDSENST00000541110ENST00000372808TRERF1chr6

42330735

-GNMTchr6

42929950

+
5UTR-3CDSENST00000372917ENST00000372808TRERF1chr6

42330735

-GNMTchr6

42929950

+
5UTR-3CDSENST00000372922ENST00000372808TRERF1chr6

42330735

-GNMTchr6

42929950

+
intron-3CDSENST00000340840ENST00000372808TRERF1chr6

42330735

-GNMTchr6

42929950

+
intron-3CDSENST00000354325ENST00000372808TRERF1chr6

42330735

-GNMTchr6

42929950

+
intron-3CDSENST00000541110ENST00000372808TRERF1chr6

42330685

-GNMTchr6

42929950

+
intron-3CDSENST00000372917ENST00000372808TRERF1chr6

42330685

-GNMTchr6

42929950

+
intron-3CDSENST00000372922ENST00000372808TRERF1chr6

42330685

-GNMTchr6

42929950

+
5UTR-3CDSENST00000340840ENST00000372808TRERF1chr6

42330685

-GNMTchr6

42929950

+
5UTR-3CDSENST00000354325ENST00000372808TRERF1chr6

42330685

-GNMTchr6

42929950

+

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 TRERF1-GNMT


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)
TRERF1chr642330734-GNMTchr642929949+1.09E-121
TRERF1chr642330684-GNMTchr642929949+9.58E-151
TRERF1chr642330734-GNMTchr642929949+1.09E-121
TRERF1chr642330684-GNMTchr642929949+9.58E-151

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 TRERF1-GNMT


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
.GNMT

Q14749

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: Catalyzes the methylation of glycine by using S-adenosylmethionine (AdoMet) to form N-methylglycine (sarcosine) with the concomitant production of S-adenosylhomocysteine (AdoHcy). Possible crucial role in the regulation of tissue concentration of AdoMet and of metabolism of methionine. {ECO:0000269|PubMed:15340920, ECO:0000269|PubMed:17660255}.

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 TRERF1-GNMT


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 TRERF1-GNMT


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 TRERF1-GNMT


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneGNMTQ14749DB00118AdemetionineCofactorSmall moleculeApproved|Investigational|Nutraceutical
TgeneGNMTQ14749DB00145GlycineSubstrateSmall moleculeApproved|Nutraceutical|Vet_approved

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Related Diseases for TRERF1-GNMT


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTRERF1C0006142Malignant neoplasm of breast1CTD_human
HgeneTRERF1C0678222Breast Carcinoma1CTD_human
HgeneTRERF1C1257931Mammary Neoplasms, Human1CTD_human
HgeneTRERF1C1458155Mammary Neoplasms1CTD_human
HgeneTRERF1C4704874Mammary Carcinoma, Human1CTD_human
TgeneGNMTC1847720Hypermethioninemia due to deficiency of glycine N-methyltransferase8CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneGNMTC0268621Hepatic methionine adenosyltransferase deficiency2CTD_human
TgeneGNMTC2239176Liver carcinoma2CTD_human
TgeneGNMTC3151058S-adenosylhomocysteine hydrolase deficiency2CTD_human
TgeneGNMTC4048705Hypermethioninemia2CTD_human
TgeneGNMTC0019158Hepatitis1CTD_human
TgeneGNMTC0019189Hepatitis, Chronic1CTD_human
TgeneGNMTC0023903Liver neoplasms1CTD_human
TgeneGNMTC0033578Prostatic Neoplasms1CTD_human
TgeneGNMTC0149519Chronic Persistent Hepatitis1CTD_human
TgeneGNMTC0345904Malignant neoplasm of liver1CTD_human
TgeneGNMTC0376358Malignant neoplasm of prostate1CTD_human
TgeneGNMTC0400966Non-alcoholic Fatty Liver Disease1CTD_human
TgeneGNMTC0520463Chronic active hepatitis1CTD_human
TgeneGNMTC0524611Cryptogenic Chronic Hepatitis1CTD_human
TgeneGNMTC0598608Hyperhomocysteinemia1CTD_human
TgeneGNMTC3241937Nonalcoholic Steatohepatitis1CTD_human