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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 28824

FusionGeneSummary for PRMT3_TCN1

check button Fusion gene summary
Fusion gene informationFusion gene name: PRMT3_TCN1
Fusion gene ID: 28824
HgeneTgene
Gene symbol

PRMT3

TCN1

Gene ID

10196

6947

Gene nameprotein arginine methyltransferase 3transcobalamin 1
SynonymsHRMT1L3HC|TC-1|TC1|TCI
Cytomap

11p15.1

11q12.1

Type of geneprotein-codingprotein-coding
Descriptionprotein arginine N-methyltransferase 3HMT1 hnRNP methyltransferase-like 3heterogeneous nuclear ribonucleoprotein methyltransferase-like protein 3transcobalamin-1haptocorinhaptocorrinprotein Rtranscobalamin I (vitamin B12 binding protein, R binder family)
Modification date2018052320180519
UniProtAcc

O60678

P20061

Ensembl transtripts involved in fusion geneENST00000331079, ENST00000437750, 
ENST00000257264, ENST00000532419, 
Fusion gene scores* DoF score1 X 1 X 1=13 X 3 X 3=27
# samples 13
** MAII scorelog2(1/1*10)=3.32192809488736log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: PRMT3 [Title/Abstract] AND TCN1 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
HgenePRMT3

GO:0031397

negative regulation of protein ubiquitination

18573314


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGALDLUSCTCGA-85-A50M-01APRMT3chr11

20486092

+TCN1chr11

59629155

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-shiftENST00000331079ENST00000257264PRMT3chr11

20486092

+TCN1chr11

59629155

-
5CDS-5UTRENST00000331079ENST00000532419PRMT3chr11

20486092

+TCN1chr11

59629155

-
Frame-shiftENST00000437750ENST00000257264PRMT3chr11

20486092

+TCN1chr11

59629155

-
5CDS-5UTRENST00000437750ENST00000532419PRMT3chr11

20486092

+TCN1chr11

59629155

-

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FusionProtFeatures for PRMT3_TCN1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PRMT3

O60678

TCN1

P20061

Methylates (mono and asymmetric dimethylation) theguanidino nitrogens of arginyl residues in some proteins. Binds vitamin B12 with femtomolar affinity and protectsit from the acidic environment of the stomach.

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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FusionGeneSequence for PRMT3_TCN1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for PRMT3_TCN1


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
PRMT3RPS2, FBL, VHL, TP53, STAT1, VCP, HNRNPA1, PPARD, RASSF2, HIRIP3, IDE, LIG1, ARFIP1, CTNNA1, EIF4B, FAF1, GFPT1, HIST1H4A, HSPH1, NARS, OSBP, PLOD2, SAMHD1, SEC23A, USP11, XRCC5, YAP1, TROVE2, XPO7, EGFR, STX19, FKBP6, PDCD2L, GMPPB, NTRK1, CNTROB, XPO1, HNRNPD, TSC22D2, KLHL10, TSKS, TSHB, TRIM25TCN1CBL, DDX31


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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RelatedDrugs for PRMT3_TCN1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneTCN1P20061DB00200HydroxocobalaminTranscobalamin-1small moleculeapproved

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RelatedDiseases for PRMT3_TCN1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneTCN1C0002888Anemia, Megaloblastic1CTD_human