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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:GFER-TRAF7 (FusionGDB2 ID:32828)

Fusion Gene Summary for GFER-TRAF7

check button Fusion gene summary
Fusion gene informationFusion gene name: GFER-TRAF7
Fusion gene ID: 32828
HgeneTgene
Gene symbol

GFER

TRAF7

Gene ID

2671

84231

Gene namegrowth factor, augmenter of liver regenerationTNF receptor associated factor 7
SynonymsALR|ERV1|HERV1|HPO|HPO1|HPO2|HSSCAFDADD|RFWD1|RNF119
Cytomap

16p13.3

16p13.3

Type of geneprotein-codingprotein-coding
DescriptionFAD-linked sulfhydryl oxidase ALRERV1 homologerv1-like growth factorhepatic regenerative stimulation substancehepatopoietin proteinE3 ubiquitin-protein ligase TRAF7RING finger and WD repeat-containing protein 1RING finger protein 119RING-type E3 ubiquitin transferase TRAF7TNF receptor-associated factor 7, E3 ubiquitin protein ligasering finger and WD repeat domain 1
Modification date2020032220200313
UniProtAcc

P55789

.
Ensembl transtripts involved in fusion geneENST00000569451, ENST00000248114, 
ENST00000567719, 
ENST00000326181, 
Fusion gene scores* DoF score1 X 1 X 1=13 X 2 X 3=18
# samples 13
** MAII scorelog2(1/1*10)=3.32192809488736log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: GFER [Title/Abstract] AND TRAF7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGFER(2034477)-TRAF7(2218078), # samples:1
Anticipated loss of major functional domain due to fusion event.GFER-TRAF7 seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
GFER-TRAF7 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
GFER-TRAF7 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
GFER-TRAF7 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
TgeneTRAF7

GO:0000185

activation of MAPKKK activity

14743216

TgeneTRAF7

GO:0006915

apoptotic process

15001576

TgeneTRAF7

GO:0016567

protein ubiquitination

14743216

TgeneTRAF7

GO:0043410

positive regulation of MAPK cascade

15001576


check buttonFusion gene breakpoints across GFER (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 TRAF7 (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
ChimerDB4MESOTCGA-ZN-A9VP-01AGFERchr16

2034477

+TRAF7chr16

2218078

+


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Fusion Gene ORF analysis for GFER-TRAF7

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-shiftENST00000569451ENST00000326181GFERchr16

2034477

+TRAF7chr16

2218078

+
Frame-shiftENST00000248114ENST00000326181GFERchr16

2034477

+TRAF7chr16

2218078

+
intron-3CDSENST00000567719ENST00000326181GFERchr16

2034477

+TRAF7chr16

2218078

+

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 GFER-TRAF7


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)
GFERchr162034477+TRAF7chr162218077+0.0014292040.9985708
GFERchr162034477+TRAF7chr162218077+0.0014292040.9985708

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 GFER-TRAF7


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
GFER

P55789

.
FUNCTION: [Isoform 1]: FAD-dependent sulfhydryl oxidase that regenerates the redox-active disulfide bonds in CHCHD4/MIA40, a chaperone essential for disulfide bond formation and protein folding in the mitochondrial intermembrane space. The reduced form of CHCHD4/MIA40 forms a transient intermolecular disulfide bridge with GFER/ERV1, resulting in regeneration of the essential disulfide bonds in CHCHD4/MIA40, while GFER/ERV1 becomes re-oxidized by donating electrons to cytochrome c or molecular oxygen. {ECO:0000269|PubMed:19397338, ECO:0000269|PubMed:20593814, ECO:0000269|PubMed:21383138, ECO:0000269|PubMed:22224850, ECO:0000269|PubMed:23186364, ECO:0000269|PubMed:23676665}.; FUNCTION: [Isoform 2]: May act as an autocrine hepatotrophic growth factor promoting liver regeneration.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.

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 GFER-TRAF7


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 GFER-TRAF7


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 GFER-TRAF7


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneGFERP55789DB03147Flavin adenine dinucleotideSmall moleculeApproved
HgeneGFERP55789DB03147Flavin adenine dinucleotideSmall moleculeApproved
HgeneGFERP55789DB03147Flavin adenine dinucleotideSmall moleculeApproved
HgeneGFERP55789DB03147Flavin adenine dinucleotideSmall moleculeApproved

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Related Diseases for GFER-TRAF7


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGFERC2751320Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay4CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneGFERC0022660Kidney Failure, Acute1CTD_human
HgeneGFERC0162557Liver Failure, Acute1CTD_human
HgeneGFERC0392622Toxic effect of carbon tetrachloride1CTD_human
HgeneGFERC1565662Acute Kidney Insufficiency1CTD_human
HgeneGFERC2609414Acute kidney injury1CTD_human
HgeneGFERC3714756Intellectual Disability1GENOMICS_ENGLAND
TgeneTRAF7C4748484CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY2GENOMICS_ENGLAND;UNIPROT
TgeneTRAF7C0018798Congenital Heart Defects1GENOMICS_ENGLAND
TgeneTRAF7C0345967Malignant mesothelioma1CTD_human
TgeneTRAF7C0557874Global developmental delay1GENOMICS_ENGLAND
TgeneTRAF7C1387925Abnormality of limbs1GENOMICS_ENGLAND
TgeneTRAF7C3550704Abnormality of digit1GENOMICS_ENGLAND