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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:TMTC2-PTPRR (FusionGDB2 ID:91879)

Fusion Gene Summary for TMTC2-PTPRR

check button Fusion gene summary
Fusion gene informationFusion gene name: TMTC2-PTPRR
Fusion gene ID: 91879
HgeneTgene
Gene symbol

TMTC2

PTPRR

Gene ID

160335

5801

Gene nametransmembrane O-mannosyltransferase targeting cadherins 2protein tyrosine phosphatase receptor type R
SynonymsIBDBP1EC-PTP|PCPTP1|PTP-SL|PTPBR7|PTPRQ
Cytomap

12q21.31

12q15

Type of geneprotein-codingprotein-coding
Descriptionprotein O-mannosyl-transferase TMTC2transmembrane and TPR repeat-containing protein 2transmembrane and tetratricopeptide repeat containing 2receptor-type tyrosine-protein phosphatase RCh-1 PTPaseNC-PTPCOM1R-PTP-Rch-1PTPaseprotein tyrosine phosphatase Cr1PTPaseprotein-tyrosine phosphatase NC-PTPCOM1protein-tyrosine phosphatase PCPTP1
Modification date2020032920200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000321196, ENST00000548305, 
ENST00000549919, 
ENST00000283228, 
ENST00000440835, ENST00000537619, 
ENST00000378778, ENST00000342084, 
ENST00000549308, 
Fusion gene scores* DoF score11 X 7 X 5=38538 X 16 X 13=7904
# samples 1142
** MAII scorelog2(11/385*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(42/7904*10)=-4.23412171391856
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TMTC2 [Title/Abstract] AND PTPRR [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointTMTC2(83081448)-PTPRR(71286757), # samples:1
Anticipated loss of major functional domain due to fusion event.TMTC2-PTPRR seems lost the major protein functional domain in Tgene 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

check buttonFusion gene breakpoints across TMTC2 (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 PTPRR (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
ChimerDB4SARCTCGA-DX-A1L4-01ATMTC2chr12

83081448

-PTPRRchr12

71286757

-


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Fusion Gene ORF analysis for TMTC2-PTPRR

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-shiftENST00000321196ENST00000283228TMTC2chr12

83081448

-PTPRRchr12

71286757

-
5CDS-intronENST00000321196ENST00000440835TMTC2chr12

83081448

-PTPRRchr12

71286757

-
5CDS-intronENST00000321196ENST00000537619TMTC2chr12

83081448

-PTPRRchr12

71286757

-
5CDS-intronENST00000321196ENST00000378778TMTC2chr12

83081448

-PTPRRchr12

71286757

-
5CDS-intronENST00000321196ENST00000342084TMTC2chr12

83081448

-PTPRRchr12

71286757

-
5CDS-intronENST00000321196ENST00000549308TMTC2chr12

83081448

-PTPRRchr12

71286757

-
Frame-shiftENST00000548305ENST00000283228TMTC2chr12

83081448

-PTPRRchr12

71286757

-
5CDS-intronENST00000548305ENST00000440835TMTC2chr12

83081448

-PTPRRchr12

71286757

-
5CDS-intronENST00000548305ENST00000537619TMTC2chr12

83081448

-PTPRRchr12

71286757

-
5CDS-intronENST00000548305ENST00000378778TMTC2chr12

83081448

-PTPRRchr12

71286757

-
5CDS-intronENST00000548305ENST00000342084TMTC2chr12

83081448

-PTPRRchr12

71286757

-
5CDS-intronENST00000548305ENST00000549308TMTC2chr12

83081448

-PTPRRchr12

71286757

-
intron-3CDSENST00000549919ENST00000283228TMTC2chr12

83081448

-PTPRRchr12

71286757

-
intron-intronENST00000549919ENST00000440835TMTC2chr12

83081448

-PTPRRchr12

71286757

-
intron-intronENST00000549919ENST00000537619TMTC2chr12

83081448

-PTPRRchr12

71286757

-
intron-intronENST00000549919ENST00000378778TMTC2chr12

83081448

-PTPRRchr12

71286757

-
intron-intronENST00000549919ENST00000342084TMTC2chr12

83081448

-PTPRRchr12

71286757

-
intron-intronENST00000549919ENST00000549308TMTC2chr12

83081448

-PTPRRchr12

71286757

-

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 TMTC2-PTPRR


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 TMTC2-PTPRR


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
..
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: 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 TMTC2-PTPRR


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 TMTC2-PTPRR


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 TMTC2-PTPRR


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 TMTC2-PTPRR


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTMTC2C0011052Prelingual Deafness1CTD_human
HgeneTMTC2C0011053Deafness1CTD_human;GENOMICS_ENGLAND
HgeneTMTC2C0086395Hearing Loss, Extreme1CTD_human
HgeneTMTC2C0581883Complete Hearing Loss1CTD_human
HgeneTMTC2C0751068Deafness, Acquired1CTD_human
HgeneTMTC2C3665473Bilateral Deafness1CTD_human
HgeneTMTC2C3711374Nonsyndromic Deafness1CLINGEN
HgeneTMTC2C4082305Deaf Mutism1CTD_human
TgenePTPRRC0041696Unipolar Depression1PSYGENET
TgenePTPRRC1269683Major Depressive Disorder1PSYGENET