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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:LRIG3-DTX3

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: LRIG3-DTX3
FusionPDB ID: 49694
FusionGDB2.0 ID: 49694
HgeneTgene
Gene symbol

LRIG3

DTX3

Gene ID

121227

196403

Gene nameleucine rich repeats and immunoglobulin like domains 3deltex E3 ubiquitin ligase 3
SynonymsLIG3RNF154|deltex3
Cytomap

12q14.1

12q13.3

Type of geneprotein-codingprotein-coding
Descriptionleucine-rich repeats and immunoglobulin-like domains protein 3LIG-3probable E3 ubiquitin-protein ligase DTX3RING finger protein 154RING-type E3 ubiquitin transferase DTX3deltex 3, E3 ubiquitin ligasedeltex homolog 3protein deltex-3
Modification date2020031320200313
UniProtAcc

Q6UXM1

Q8TDB6

Ensembl transtripts involved in fusion geneENST idsENST00000320743, ENST00000379141, 
ENST00000337737, ENST00000548198, 
ENST00000548804, ENST00000551632, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score10 X 8 X 8=6405 X 6 X 4=120
# samples 127
** MAII scorelog2(12/640*10)=-2.41503749927884
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/120*10)=-0.777607578663552
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: LRIG3 [Title/Abstract] AND DTX3 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)LRIG3(59307763)-DTX3(58002860), # samples:1
Anticipated loss of major functional domain due to fusion event.LRIG3-DTX3 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.
LRIG3-DTX3 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.
LRIG3-DTX3 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.
LRIG3-DTX3 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.
LRIG3-DTX3 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
LRIG3-DTX3 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
LRIG3-DTX3 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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 LRIG3 (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 DTX3 (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
ChimerDB4BRCATCGA-AR-A1AH-01ALRIG3chr12

59307763

-DTX3chr12

58002860

+


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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)
ENST00000379141LRIG3chr1259307763-ENST00000551632DTX3chr1258002860+995267567139142
ENST00000320743LRIG3chr1259307763-ENST00000551632DTX3chr1258002860+1398670221745174

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
ENST00000379141ENST00000551632LRIG3chr1259307763-DTX3chr1258002860+0.449301870.55069816
ENST00000320743ENST00000551632LRIG3chr1259307763-DTX3chr1258002860+0.584872960.415127

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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

>49694_49694_1_LRIG3-DTX3_LRIG3_chr12_59307763_ENST00000320743_DTX3_chr12_58002860_ENST00000551632_length(amino acids)=174AA_BP=150
MCRAPSARRLGASGRDLGRWTAMSAPSLRARAAGLGLLLCAVLGRAGRSDSGGRGELGQPSGVAAERPCPTTCRCLGDLLDCSRKRLARL

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

>49694_49694_2_LRIG3-DTX3_LRIG3_chr12_59307763_ENST00000379141_DTX3_chr12_58002860_ENST00000551632_length(amino acids)=142AA_BP=1
MEVGLCQKGVAHTALKHLASGGWGKGLPPPSRNSLPSQTGPLQVWCGGQGAERRKRLLLGPSRGRQQGPWQRRCPSVICDTLRSQLLLHP

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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/chr12:59307763/chr12:58002860)
- 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
LRIG3

Q6UXM1

DTX3

Q8TDB6

FUNCTION: May play a role in craniofacial and inner ear morphogenesis during embryonic development. May act within the otic vesicle epithelium to control formation of the lateral semicircular canal in the inner ear, possibly by restricting the expression of NTN1 (By similarity). {ECO:0000250}.FUNCTION: E3 ubiquitin-protein ligase which, in association with ADP-ribosyltransferase PARP9, plays a role in DNA damage repair and in interferon-mediated antiviral responses (PubMed:12670957, PubMed:19818714, PubMed:26479788, PubMed:23230272). Monoubiquitinates several histones, including histone H2A, H2B, H3 and H4 (PubMed:28525742). In response to DNA damage, mediates monoubiquitination of 'Lys-91' of histone H4 (H4K91ub1) (PubMed:19818714). The exact role of H4K91ub1 in DNA damage response is still unclear but it may function as a licensing signal for additional histone H4 post-translational modifications such as H4 'Lys-20' methylation (H4K20me) (PubMed:19818714). PARP1-dependent PARP9-DTX3L-mediated ubiquitination promotes the rapid and specific recruitment of 53BP1/TP53BP1, UIMC1/RAP80, and BRCA1 to DNA damage sites (PubMed:23230272). By monoubiquitinating histone H2B H2BC9/H2BJ and thereby promoting chromatin remodeling, positively regulates STAT1-dependent interferon-stimulated gene transcription and thus STAT1-mediated control of viral replication (PubMed:26479788). Independently of its catalytic activity, promotes the sorting of chemokine receptor CXCR4 from early endosome to lysosome following CXCL12 stimulation by reducing E3 ligase ITCH activity and thus ITCH-mediated ubiquitination of endosomal sorting complex required for transport ESCRT-0 components HGS and STAM (PubMed:24790097). In addition, required for the recruitment of HGS and STAM to early endosomes (PubMed:24790097). In association with PARP9, plays a role in antiviral responses by mediating 'Lys-48'-linked ubiquitination of encephalomyocarditis virus (EMCV) and human rhinovirus (HRV) C3 proteases and thus promoting their proteosomal-mediated degradation (PubMed:26479788). {ECO:0000269|PubMed:12670957, ECO:0000269|PubMed:19818714, ECO:0000269|PubMed:23230272, ECO:0000269|PubMed:24790097, ECO:0000269|PubMed:26479788, ECO:0000269|PubMed:28525742}.

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
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-31938_74127.666666666666671120.0DomainNote=LRRNT
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-31975_96127.666666666666671120.0RepeatNote=LRR 1
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-31999_120127.666666666666671120.0RepeatNote=LRR 2

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319444_495127.666666666666671120.0DomainNote=LRRCT
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319499_598127.666666666666671120.0DomainNote=Ig-like C2-type 1
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319603_692127.666666666666671120.0DomainNote=Ig-like C2-type 2
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319697_783127.666666666666671120.0DomainNote=Ig-like C2-type 3
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-31938_7467.666666666666671060.0DomainNote=LRRNT
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319444_49567.666666666666671060.0DomainNote=LRRCT
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319499_59867.666666666666671060.0DomainNote=Ig-like C2-type 1
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319603_69267.666666666666671060.0DomainNote=Ig-like C2-type 2
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319697_78367.666666666666671060.0DomainNote=Ig-like C2-type 3
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319122_142127.666666666666671120.0RepeatNote=LRR 3
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319146_167127.666666666666671120.0RepeatNote=LRR 4
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319168_189127.666666666666671120.0RepeatNote=LRR 5
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319193_214127.666666666666671120.0RepeatNote=LRR 6
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319216_237127.666666666666671120.0RepeatNote=LRR 7
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319240_261127.666666666666671120.0RepeatNote=LRR 8
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319264_285127.666666666666671120.0RepeatNote=LRR 9
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319288_309127.666666666666671120.0RepeatNote=LRR 10
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319312_333127.666666666666671120.0RepeatNote=LRR 11
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319336_357127.666666666666671120.0RepeatNote=LRR 12
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319360_382127.666666666666671120.0RepeatNote=LRR 13
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319387_408127.666666666666671120.0RepeatNote=LRR 14
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319411_432127.666666666666671120.0RepeatNote=LRR 15
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319122_14267.666666666666671060.0RepeatNote=LRR 3
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319146_16767.666666666666671060.0RepeatNote=LRR 4
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319168_18967.666666666666671060.0RepeatNote=LRR 5
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319193_21467.666666666666671060.0RepeatNote=LRR 6
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319216_23767.666666666666671060.0RepeatNote=LRR 7
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319240_26167.666666666666671060.0RepeatNote=LRR 8
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319264_28567.666666666666671060.0RepeatNote=LRR 9
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319288_30967.666666666666671060.0RepeatNote=LRR 10
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319312_33367.666666666666671060.0RepeatNote=LRR 11
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319336_35767.666666666666671060.0RepeatNote=LRR 12
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319360_38267.666666666666671060.0RepeatNote=LRR 13
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319387_40867.666666666666671060.0RepeatNote=LRR 14
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319411_43267.666666666666671060.0RepeatNote=LRR 15
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-31975_9667.666666666666671060.0RepeatNote=LRR 1
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-31999_12067.666666666666671060.0RepeatNote=LRR 2
HgeneLRIG3chr12:59307763chr12:58002860ENST00000320743-319810_830127.666666666666671120.0TransmembraneHelical
HgeneLRIG3chr12:59307763chr12:58002860ENST00000379141-319810_83067.666666666666671060.0TransmembraneHelical
TgeneDTX3chr12:59307763chr12:58002860ENST0000033773757122_151322.6666666666667348.0Compositional biasNote=Pro-rich
TgeneDTX3chr12:59307763chr12:58002860ENST0000054819835122_151322.6666666666667348.0Compositional biasNote=Pro-rich
TgeneDTX3chr12:59307763chr12:58002860ENST0000054880446122_151322.6666666666667348.0Compositional biasNote=Pro-rich
TgeneDTX3chr12:59307763chr12:58002860ENST0000055163246122_151325.6666666666667351.0Compositional biasNote=Pro-rich
TgeneDTX3chr12:59307763chr12:58002860ENST0000033773757164_205322.6666666666667348.0Zinc fingerRING-type
TgeneDTX3chr12:59307763chr12:58002860ENST0000054819835164_205322.6666666666667348.0Zinc fingerRING-type
TgeneDTX3chr12:59307763chr12:58002860ENST0000054880446164_205322.6666666666667348.0Zinc fingerRING-type
TgeneDTX3chr12:59307763chr12:58002860ENST0000055163246164_205325.6666666666667351.0Zinc fingerRING-type


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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
LRIG3CAND1, TAZ, TNFSF13B, PVRIG, GINM1, LPAR6, PTPRK, PTGER3, GAL3ST1, LRIG1, LRRN2, TMPRSS3, EGFR, ERBB2, ERBB4, KIAA1429, MTDH, PSMD14, ORF3a, E, M, nsp4, nsp6, nsp9, ORF6, ORF7a, ORF7b, TRIM66, LMO7, LIMCH1, ELOVL5, GJA1, HSD17B11, METTL7A, STX4, PDE3A, CLEC12B, SPSB4, OR10H1, CLGN, FBXO2, TMPRSS13, NRSN1, RLN1, RARRES1, LRRC4C, CLEC4A, SPSB2, ANPEP, DPP4, TMPRSS4,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
LRIG3all structure
DTX3


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


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Related Drugs to LRIG3-DTX3


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 LRIG3-DTX3


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