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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: 31348

FusionGeneSummary for RNASEH1_DYSF

check button Fusion gene summary
Fusion gene informationFusion gene name: RNASEH1_DYSF
Fusion gene ID: 31348
HgeneTgene
Gene symbol

RNASEH1

DYSF

Gene ID

246243

8291

Gene nameribonuclease H1dysferlin
SynonymsH1RNA|PEOB2|RNH1FER1L1|LGMD2B|MMD1
Cytomap

2p25.3

2p13.2

Type of geneprotein-codingprotein-coding
Descriptionribonuclease H1ribonuclease H type IIdysferlindystrophy-associated fer-1-like 1fer-1-like family member 1fer-1-like protein 1limb girdle muscular dystrophy 2B (autosomal recessive)
Modification date2018052320180519
UniProtAcc

O60930

O75923

Ensembl transtripts involved in fusion geneENST00000315212, ENST00000429174, 
ENST00000409762, ENST00000413539, 
ENST00000409582, ENST00000258104, 
ENST00000410020, ENST00000409744, 
ENST00000409651, ENST00000410041, 
ENST00000409366, ENST00000394120, 
ENST00000479049, 
Fusion gene scores* DoF score1 X 1 X 1=14 X 4 X 3=48
# samples 15
** MAII scorelog2(1/1*10)=3.32192809488736log2(5/48*10)=0.0588936890535686
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: RNASEH1 [Title/Abstract] AND DYSF [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

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
TCGARVSKCMTCGA-DA-A95Y-06ARNASEH1chr2

3599734

-DYSFchr2

71871095

+
* 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-shiftENST00000315212ENST00000429174RNASEH1chr2

3599734

-DYSFchr2

71871095

+
Frame-shiftENST00000315212ENST00000409762RNASEH1chr2

3599734

-DYSFchr2

71871095

+
Frame-shiftENST00000315212ENST00000413539RNASEH1chr2

3599734

-DYSFchr2

71871095

+
Frame-shiftENST00000315212ENST00000409582RNASEH1chr2

3599734

-DYSFchr2

71871095

+
Frame-shiftENST00000315212ENST00000258104RNASEH1chr2

3599734

-DYSFchr2

71871095

+
Frame-shiftENST00000315212ENST00000410020RNASEH1chr2

3599734

-DYSFchr2

71871095

+
Frame-shiftENST00000315212ENST00000409744RNASEH1chr2

3599734

-DYSFchr2

71871095

+
Frame-shiftENST00000315212ENST00000409651RNASEH1chr2

3599734

-DYSFchr2

71871095

+
Frame-shiftENST00000315212ENST00000410041RNASEH1chr2

3599734

-DYSFchr2

71871095

+
Frame-shiftENST00000315212ENST00000409366RNASEH1chr2

3599734

-DYSFchr2

71871095

+
Frame-shiftENST00000315212ENST00000394120RNASEH1chr2

3599734

-DYSFchr2

71871095

+
5CDS-3UTRENST00000315212ENST00000479049RNASEH1chr2

3599734

-DYSFchr2

71871095

+

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FusionProtFeatures for RNASEH1_DYSF


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RNASEH1

O60930

DYSF

O75923

Endonuclease that specifically degrades the RNA of RNA-DNA hybrids (PubMed:10497183). Plays a role in RNA polymerase II(RNAp II) transcription termination by degrading R-loop RNA-DNAhybrid formation at G-rich pause sites located downstream of thepoly(A) site and behind the elongating RNAp II (PubMed:21700224).{ECO:0000269|PubMed:10497183, ECO:0000269|PubMed:21700224}.

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 RNASEH1_DYSF


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 RNASEH1_DYSF


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
RNASEH1ELAVL1, TM9SF1, RPA1, RPA2, RPA3, LUC7L, FOXD4, CHCHD10, CHCHD2, CLEC3A, TRIM25DYSFCAV3, HDAC6, HECW2, FAM65B, HNRNPD, FTSJ1, SGOL1


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 RNASEH1_DYSF


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

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RelatedDiseases for RNASEH1_DYSF


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRNASEH1C4225312PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 21UNIPROT
TgeneDYSFC1850808Miyoshi myopathy19CTD_human;ORPHANET;UNIPROT
TgeneDYSFC1850889MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B8CTD_human;ORPHANET;UNIPROT
TgeneDYSFC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneDYSFC3495559Juvenile arthritis1CTD_human