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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:UST-GINM1 (FusionGDB2 ID:97027)

Fusion Gene Summary for UST-GINM1

check button Fusion gene summary
Fusion gene informationFusion gene name: UST-GINM1
Fusion gene ID: 97027
HgeneTgene
Gene symbol

UST

GINM1

Gene ID

10090

116254

Gene nameuronyl 2-sulfotransferaseglycoprotein integral membrane 1
Synonyms2OSTC6orf72
Cytomap

6q25.1

6q25.1

Type of geneprotein-codingprotein-coding
Descriptionuronyl 2-sulfotransferasedermatan/chondroitin sulfate 2-sulfotransferaseglycoprotein integral membrane protein 1
Modification date2020031320200313
UniProtAcc.

Q9NU53

Ensembl transtripts involved in fusion geneENST00000367463, ENST00000466695, 
ENST00000367419, 
Fusion gene scores* DoF score10 X 8 X 5=4004 X 3 X 4=48
# samples 124
** MAII scorelog2(12/400*10)=-1.73696559416621
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: UST [Title/Abstract] AND GINM1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointUST(149285699)-GINM1(149893421), # 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

check buttonFusion gene breakpoints across UST (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 GINM1 (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
ChimerDB4GBMTCGA-26-5133-01AUSTchr6

149285699

+GINM1chr6

149893421

+


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Fusion Gene ORF analysis for UST-GINM1

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
In-frameENST00000367463ENST00000367419USTchr6

149285699

+GINM1chr6

149893421

+
intron-3CDSENST00000466695ENST00000367419USTchr6

149285699

+GINM1chr6

149893421

+

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)
ENST00000367463USTchr6149285699+ENST00000367419GINM1chr6149893421+2567784791656525

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
ENST00000367463ENST00000367419USTchr6149285699+GINM1chr6149893421+0.0002367350.9997633

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Fusion Genomic Features for UST-GINM1


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)
USTchr6149285699+GINM1chr6149893420+0.0004052190.99959475
USTchr6149285699+GINM1chr6149893420+0.0004052190.99959475

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 UST-GINM1


check button Go to

FGviewer for the breakpoints of chr6:149285699-chr6:149893421

.
- 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
.GINM1

Q9NU53

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
HgeneUSTchr6:149285699chr6:149893421ENST00000367463+581_49227.0407.0Topological domainCytoplasmic
HgeneUSTchr6:149285699chr6:149893421ENST00000367463+5850_70227.0407.0TransmembraneHelical%3B Signal-anchor for type II membrane protein
TgeneGINM1chr6:149285699chr6:149893421ENST0000036741908290_33040.0331.0Topological domainCytoplasmic
TgeneGINM1chr6:149285699chr6:149893421ENST0000036741908269_28940.0331.0TransmembraneHelical

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneUSTchr6:149285699chr6:149893421ENST00000367463+5871_406227.0407.0Topological domainLumenal
TgeneGINM1chr6:149285699chr6:149893421ENST000003674190824_26840.0331.0Topological domainExtracellular


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Fusion Gene Sequence for UST-GINM1


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.
>In-frame_ENST00000367463_ENST00000367419_TCGA-26-5133-01A_UST_chr6_149285699_+_GINM1_chr6_149893421_length(transcript)=2567nt_BP=784nt
CGGCCCTCCCCATGTGCAGCCGGCCAGCCGGGCTCTCCTCCTCGCGGCGGATGGGTGACCTTTTCCTGGCACGGGCAGGCTGTGGGAGGC
AGCGGAGCAGGCGATGAAGAAGAAGCAGCAGCATCCCGGCGGCGGCGCGGATCCCTGGCCCCATGGGGCCCCTATGGGGGGCGCCCCTCC
GGGCCTGGGCAGCTGGAAGCGTCGGGTGCCCCTGCTGCCTTTCCTGCGCTTCTCCCTCCGGGACTACGGCTTCTGCATGGCCACCCTGCT
GGTCTTCTGCCTGGGCTCCCTCCTCTATCAGCTCAGCGGGGGACCCCCTCGCTTCCTGCTCGACCTGCGGCAGTACTTGGGAAATTCCAC
TTACTTGGATGACCATGGACCACCTCCTAGTAAGGTACTACCTTTCCCAAGCCAGGTGGTGTACAACAGGGTAGGCAAGTGTGGGAGCCG
TACTGTGGTCTTGCTTCTGAGAATCTTGTCGGAGAAGCACGGATTTAATTTGGTCACATCAGACATTCACAACAAAACCAGGCTTACTAA
AAATGAACAAATGGAACTGATTAAAAATATAAGTACTGCCGAACAACCCTATTTATTCACTCGACATGTTCATTTCCTCAACTTCTCAAG
GTTTGGAGGAGACCAGCCTGTCTACATCAACATCATTAGAGACCCCGTCAACCGGTTCTTATCCAACTATTTTTTCCGTCGCTTTGGAGA
CTGGAGAGGGGAACAAAATCACATGATCCGCACCCCCAGCATGAGGCAGGAGGAGCGCTACCTGGACGGCATCAGAATTAATGTAACTAC
ACTGAAAGATGATGGGGACATATCTAAACAGCAGGTTGTTCTTAACATAACCTATGAGAGTGGACAGGTGTATGTAAATGACTTACCTGT
AAATAGTGGTGTAACCCGAATAAGCTGTCAGACTTTGATAGTGAAGAATGAAAATCTTGAAAATTTGGAGGAAAAAGAATATTTTGGAAT
TGTCAGTGTAAGGATTTTAGTTCATGAGTGGCCTATGACATCTGGTTCCAGTTTGCAACTAATTGTCATTCAAGAAGAGGTAGTAGAGAT
TGATGGAAAACAAGTTCAGCAAAAGGATGTCACTGAAATTGATATTTTAGTTAAGAACCGGGGAGTACTCAGACATTCAAACTATACCCT
CCCTTTGGAAGAAAGCATGCTCTACTCTATTTCTCGAGACAGTGACATTTTATTTACCCTTCCTAACCTCTCCAAAAAAGAAAGTGTTAG
TTCACTGCAAACCACTAGCCAGTATCTTATCAGGAATGTGGAAACCACTGTAGATGAAGATGTTTTACCTGGCAAGTTACCTGAAACTCC
TCTCAGAGCAGAGCCGCCATCTTCATATAAGGTAATGTGTCAGTGGATGGAAAAGTTTAGAAAAGATCTGTGTAGGTTCTGGAGCAACGT
TTTCCCAGTATTCTTTCAGTTTTTGAACATCATGGTGGTTGGAATTACAGGAGCAGCTGTGGTAATAACCATCTTAAAGGTGTTTTTCCC
AGTTTCTGAATACAAAGGAATTCTTCAGTTGGATAAAGTGGACGTCATACCTGTGACAGCTATCAACTTATATCCAGATGGTCCAGAGAA
AAGAGCTGAAAACCTTGAAGATAAAACATGTATTTAAAACGCCATCTCATATCATGGACTCCGAAGTAGCCTGTTGCCTCCAAATTTGCC
ACTTGAATATAATTTTCTTTAAATCGTTAAGAATCAGTTTATACACTAGAGAAATTGCTAAACTCTAAGACTGCCTGAAAATTGACCTTT
ACAGTGCCAAGTTAAAGTTTACCTTATTCTCGGCCGGGTGCAGTGGCTCATGCCTGTAATCCCAGGACTTTGGGAGGCCAATGCGGGCGG
ATCACGAGGTCAGATCAAGACCATCCTGCCAACATGGTGAAACCCTGTCTCTACTAAAAAAAATAAAAAAATTAGCTGGGTGTGGCGGTG
CACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCGGAGGCTGCAGTGAGCCAAGATCACGCC
ACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCTGTTTCAAAAAAAAAAAAGTTGACCTTATTCTCTAAAAGGGCTGGCTATTCATATG
ATGAATTGTTAAGGAAAACTTAAAGTGGAAGAGAACACATGTGAAGAGACTTTGAAATTATCAAAAGAAAAAAAAAAGACCAGACAAAAT
CTCATGTGCCAATAACTTTTCAAGGTGCCTTTGTTAAGGAAATTATATCCACTTAATTACTATAATATATAAGACTTTATGAAAAGCACT
TTATAAAATTCTAATTTAAAAGGTCAAGAACTTAACACTTATTTTTTTATTCAGTACAGTGTGCCTTTATATTAAGTATGTGACTCAGTA
TAAAATCACTGAAGTGTATCATGATTTGATTGTATCCTGTACCAAGACTACTTACCTTGAATGCTCCAAGATTTAAAAGTAGTATGACAT

>In-frame_ENST00000367463_ENST00000367419_TCGA-26-5133-01A_UST_chr6_149285699_+_GINM1_chr6_149893421_length(amino acids)=525AA_start in transcript=79_stop in transcript=1656
MWEAAEQAMKKKQQHPGGGADPWPHGAPMGGAPPGLGSWKRRVPLLPFLRFSLRDYGFCMATLLVFCLGSLLYQLSGGPPRFLLDLRQYL
GNSTYLDDHGPPPSKVLPFPSQVVYNRVGKCGSRTVVLLLRILSEKHGFNLVTSDIHNKTRLTKNEQMELIKNISTAEQPYLFTRHVHFL
NFSRFGGDQPVYINIIRDPVNRFLSNYFFRRFGDWRGEQNHMIRTPSMRQEERYLDGIRINVTTLKDDGDISKQQVVLNITYESGQVYVN
DLPVNSGVTRISCQTLIVKNENLENLEEKEYFGIVSVRILVHEWPMTSGSSLQLIVIQEEVVEIDGKQVQQKDVTEIDILVKNRGVLRHS
NYTLPLEESMLYSISRDSDILFTLPNLSKKESVSSLQTTSQYLIRNVETTVDEDVLPGKLPETPLRAEPPSSYKVMCQWMEKFRKDLCRF

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Fusion Gene PPI Analysis for UST-GINM1


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 UST-GINM1


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 UST-GINM1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneUSTC0004238Atrial Fibrillation2CTD_human
HgeneUSTC0235480Paroxysmal atrial fibrillation2CTD_human
HgeneUSTC2585653Persistent atrial fibrillation2CTD_human
HgeneUSTC3468561familial atrial fibrillation2CTD_human
HgeneUSTC0014175Endometriosis1CTD_human
HgeneUSTC0269102Endometrioma1CTD_human