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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:RNF19A-F10

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RNF19A-F10
FusionPDB ID: 74927
FusionGDB2.0 ID: 74927
HgeneTgene
Gene symbol

RNF19A

F10

Gene ID

25897

83541

Gene namering finger protein 19A, RBR E3 ubiquitin protein ligasefamily with sequence similarity 110 member A
SynonymsRNF19C20orf55|F10|bA371L19.3
Cytomap

8q22.2

20p13

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase RNF19Adouble ring-finger proteinprotein p38 interacting with transcription factor Sp1ring finger protein 19ring finger protein 19A, E3 ubiquitin protein ligasering-IBR-ring domain containing protein Dorfinprotein FAM110A
Modification date2020031320200313
UniProtAcc.

P00742

Ensembl transtripts involved in fusion geneENST idsENST00000341084, ENST00000519449, 
ENST00000523255, 
ENST00000483537, 
ENST00000375551, ENST00000375559, 
ENST00000409306, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score20 X 21 X 10=42006 X 7 X 4=168
# samples 347
** MAII scorelog2(34/4200*10)=-3.62678267641578
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/168*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: RNF19A [Title/Abstract] AND F10 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RNF19A(101299729)-F10(113792771), # samples:1
Anticipated loss of major functional domain due to fusion event.RNF19A-F10 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
RNF19A-F10 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
RNF19A-F10 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
RNF19A-F10 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame 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 RNF19A (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across F10 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4ESCATCGA-VR-A8EX-01ARNF19Achr8

101299729

-F10chr13

113792771

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000341084RNF19Achr8101299729-ENST00000409306F10chr13113792771+240512285541336260
ENST00000341084RNF19Achr8101299729-ENST00000375551F10chr13113792771+246412285541336260
ENST00000341084RNF19Achr8101299729-ENST00000375559F10chr13113792771+2476122812222463413
ENST00000519449RNF19Achr8101299729-ENST00000409306F10chr13113792771+21689913171099260
ENST00000519449RNF19Achr8101299729-ENST00000375551F10chr13113792771+22279913171099260
ENST00000519449RNF19Achr8101299729-ENST00000375559F10chr13113792771+22399919852226413

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
ENST00000341084ENST00000409306RNF19Achr8101299729-F10chr13113792771+0.0169960320.983004
ENST00000341084ENST00000375551RNF19Achr8101299729-F10chr13113792771+0.0172541810.98274577
ENST00000341084ENST00000375559RNF19Achr8101299729-F10chr13113792771+0.0172289740.982771
ENST00000519449ENST00000409306RNF19Achr8101299729-F10chr13113792771+0.0201225620.9798774
ENST00000519449ENST00000375551RNF19Achr8101299729-F10chr13113792771+0.0200949310.9799051
ENST00000519449ENST00000375559RNF19Achr8101299729-F10chr13113792771+0.0197330660.9802669

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>74927_74927_1_RNF19A-F10_RNF19A_chr8_101299729_ENST00000341084_F10_chr13_113792771_ENST00000375551_length(amino acids)=260AA_BP=225
MQEQEIGFISKYNEGLCVNTDPVSILTSILDMSLHRQMGSDRDLQSSASSVSLPSVKKAPKKRRISIGSLFRRKKDNKRKSRELNGGVDG
IASIESIHSEMCTDKNSIFSTNTSSDNGLTSISKQIGDFIECPLCLLRHSKDRFPDIMTCHHRSCVDCLRQYLRIEISESRVNISCPECT

--------------------------------------------------------------

>74927_74927_2_RNF19A-F10_RNF19A_chr8_101299729_ENST00000341084_F10_chr13_113792771_ENST00000375559_length(amino acids)=413AA_BP=2
MWNEFWNKYKDGDQCETSPCQNQGKCKDGLGEYTCTCLEGFEGKNCELFTRKLCSLDNGDCDQFCHEEQNSVVCSCARGYTLADNGKACI
PTGPYPCGKQTLERRKRSVAQATSSSGEAPDSITWKPYDAADLDPTENPFDLLDFNQTQPERGDNNLTRIVGGQECKDGECPWQALLINE
ENEGFCGGTILSEFYILTAAHCLYQAKRFKVRVGDRNTEQEEGGEAVHEVEVVIKHNRFTKETYDFDIAVLRLKTPITFRMNVAPACLPE
RDWAESTLMTQKTGIVSGFGRTHEKGRQSTRLKMLEVPYVDRNSCKLSSSFIITQNMFCAGYDTKQEDACQGDSGGPHVTRFKDTYFVTG

--------------------------------------------------------------

>74927_74927_3_RNF19A-F10_RNF19A_chr8_101299729_ENST00000341084_F10_chr13_113792771_ENST00000409306_length(amino acids)=260AA_BP=225
MQEQEIGFISKYNEGLCVNTDPVSILTSILDMSLHRQMGSDRDLQSSASSVSLPSVKKAPKKRRISIGSLFRRKKDNKRKSRELNGGVDG
IASIESIHSEMCTDKNSIFSTNTSSDNGLTSISKQIGDFIECPLCLLRHSKDRFPDIMTCHHRSCVDCLRQYLRIEISESRVNISCPECT

--------------------------------------------------------------

>74927_74927_4_RNF19A-F10_RNF19A_chr8_101299729_ENST00000519449_F10_chr13_113792771_ENST00000375551_length(amino acids)=260AA_BP=225
MQEQEIGFISKYNEGLCVNTDPVSILTSILDMSLHRQMGSDRDLQSSASSVSLPSVKKAPKKRRISIGSLFRRKKDNKRKSRELNGGVDG
IASIESIHSEMCTDKNSIFSTNTSSDNGLTSISKQIGDFIECPLCLLRHSKDRFPDIMTCHHRSCVDCLRQYLRIEISESRVNISCPECT

--------------------------------------------------------------

>74927_74927_5_RNF19A-F10_RNF19A_chr8_101299729_ENST00000519449_F10_chr13_113792771_ENST00000375559_length(amino acids)=413AA_BP=2
MWNEFWNKYKDGDQCETSPCQNQGKCKDGLGEYTCTCLEGFEGKNCELFTRKLCSLDNGDCDQFCHEEQNSVVCSCARGYTLADNGKACI
PTGPYPCGKQTLERRKRSVAQATSSSGEAPDSITWKPYDAADLDPTENPFDLLDFNQTQPERGDNNLTRIVGGQECKDGECPWQALLINE
ENEGFCGGTILSEFYILTAAHCLYQAKRFKVRVGDRNTEQEEGGEAVHEVEVVIKHNRFTKETYDFDIAVLRLKTPITFRMNVAPACLPE
RDWAESTLMTQKTGIVSGFGRTHEKGRQSTRLKMLEVPYVDRNSCKLSSSFIITQNMFCAGYDTKQEDACQGDSGGPHVTRFKDTYFVTG

--------------------------------------------------------------

>74927_74927_6_RNF19A-F10_RNF19A_chr8_101299729_ENST00000519449_F10_chr13_113792771_ENST00000409306_length(amino acids)=260AA_BP=225
MQEQEIGFISKYNEGLCVNTDPVSILTSILDMSLHRQMGSDRDLQSSASSVSLPSVKKAPKKRRISIGSLFRRKKDNKRKSRELNGGVDG
IASIESIHSEMCTDKNSIFSTNTSSDNGLTSISKQIGDFIECPLCLLRHSKDRFPDIMTCHHRSCVDCLRQYLRIEISESRVNISCPECT

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr8:101299729/chr13:113792771)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.F10

P00742

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: Factor Xa is a vitamin K-dependent glycoprotein that converts prothrombin to thrombin in the presence of factor Va, calcium and phospholipid during blood clotting.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRNF19Achr8:101299729chr13:113792771ENST00000341084-210132_179224.66666666666666839.0Zinc fingerRING-type 1
HgeneRNF19Achr8:101299729chr13:113792771ENST00000519449-311132_179224.66666666666666839.0Zinc fingerRING-type 1
TgeneF10chr8:101299729chr13:113792771ENST0000037555918125_16577.0489.0DomainEGF-like 2
TgeneF10chr8:101299729chr13:113792771ENST0000037555918235_46777.0489.0DomainPeptidase S1
TgeneF10chr8:101299729chr13:113792771ENST000003755591886_12277.0489.0DomainEGF-like 1%3B calcium-binding
TgeneF10chr8:101299729chr13:113792771ENST0000037555918183_20377.0489.0RegionNote=O-glycosylated at one site
TgeneF10chr8:101299729chr13:113792771ENST0000037555918476_48577.0489.0RegionNote=O-glycosylated at one site

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRNF19Achr8:101299729chr13:113792771ENST00000341084-210128_351224.66666666666666839.0RegionTRIAD supradomain
HgeneRNF19Achr8:101299729chr13:113792771ENST00000519449-311128_351224.66666666666666839.0RegionTRIAD supradomain
HgeneRNF19Achr8:101299729chr13:113792771ENST00000341084-210368_388224.66666666666666839.0TransmembraneHelical
HgeneRNF19Achr8:101299729chr13:113792771ENST00000341084-210424_444224.66666666666666839.0TransmembraneHelical
HgeneRNF19Achr8:101299729chr13:113792771ENST00000519449-311368_388224.66666666666666839.0TransmembraneHelical
HgeneRNF19Achr8:101299729chr13:113792771ENST00000519449-311424_444224.66666666666666839.0TransmembraneHelical
HgeneRNF19Achr8:101299729chr13:113792771ENST00000341084-210199_264224.66666666666666839.0Zinc fingerIBR-type
HgeneRNF19Achr8:101299729chr13:113792771ENST00000341084-210301_332224.66666666666666839.0Zinc fingerRING-type 2%3B atypical
HgeneRNF19Achr8:101299729chr13:113792771ENST00000519449-311199_264224.66666666666666839.0Zinc fingerIBR-type
HgeneRNF19Achr8:101299729chr13:113792771ENST00000519449-311301_332224.66666666666666839.0Zinc fingerRING-type 2%3B atypical
TgeneF10chr8:101299729chr13:113792771ENST000003755591841_8577.0489.0DomainGla


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
RNF19A
F10


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
HgeneRNF19Achr8:101299729chr13:113792771ENST00000341084-210660_838224.66666666666666839.0CASR
HgeneRNF19Achr8:101299729chr13:113792771ENST00000519449-311660_838224.66666666666666839.0CASR


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Related Drugs to RNF19A-F10


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to RNF19A-F10


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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