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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:RUNX3-LDLRAP1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RUNX3-LDLRAP1
FusionPDB ID: 78714
FusionGDB2.0 ID: 78714
HgeneTgene
Gene symbol

RUNX3

LDLRAP1

Gene ID

864

26119

Gene nameRUNX family transcription factor 3low density lipoprotein receptor adaptor protein 1
SynonymsAML2|CBFA3|PEBP2aCARH|ARH1|ARH2|FHCB1|FHCB2|FHCL4
Cytomap

1p36.11

1p36.11

Type of geneprotein-codingprotein-coding
Descriptionrunt-related transcription factor 3CBF-alpha-3PEA2 alpha CPEBP2 alpha CSL3-3 enhancer factor 1 alpha C subunitSL3/AKV core-binding factor alpha C subunitacute myeloid leukemia 2 proteinacute myeloid leukemia gene 2core-binding factor subunit alphalow density lipoprotein receptor adapter protein 1LDL receptor adaptor proteinautosomal recessive hypercholesterolemia protein
Modification date2020031320200313
UniProtAcc.

Q5SW96

Ensembl transtripts involved in fusion geneENST idsENST00000308873, ENST00000338888, 
ENST00000399916, ENST00000540420, 
ENST00000496967, 
ENST00000488127, 
ENST00000374338, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 4 X 3=361 X 1 X 1=1
# samples 41
** MAII scorelog2(4/36*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context (manual curation of fusion genes in FusionPDB)

PubMed: RUNX3 [Title/Abstract] AND LDLRAP1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RUNX3(25245730)-LDLRAP1(25880412), # samples:1
Anticipated loss of major functional domain due to fusion event.RUNX3-LDLRAP1 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.
RUNX3-LDLRAP1 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.
RUNX3-LDLRAP1 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.
RUNX3-LDLRAP1 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.
RUNX3-LDLRAP1 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF.
RUNX3-LDLRAP1 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
RUNX3-LDLRAP1 seems lost the major protein functional domain in Tgene partner, which is a cell metabolism 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
HgeneRUNX3

GO:0006468

protein phosphorylation

20100835

HgeneRUNX3

GO:0045893

positive regulation of transcription, DNA-templated

20599712

HgeneRUNX3

GO:0071559

response to transforming growth factor beta

20599712

TgeneLDLRAP1

GO:0006898

receptor-mediated endocytosis

14528014


check buttonFusion gene breakpoints across RUNX3 (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 LDLRAP1 (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
ChimerDB4OVTCGA-24-1548RUNX3chr1

25245730

-LDLRAP1chr1

25880412

+


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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)
ENST00000399916RUNX3chr125245730-ENST00000374338LDLRAP1chr125880412+375810254391863474
ENST00000308873RUNX3chr125245730-ENST00000374338LDLRAP1chr125880412+328655391391460
ENST00000540420RUNX3chr125245730-ENST00000374338LDLRAP1chr125880412+3077344791182367

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
ENST00000399916ENST00000374338RUNX3chr125245730-LDLRAP1chr125880412+0.0066670680.9933329
ENST00000308873ENST00000374338RUNX3chr125245730-LDLRAP1chr125880412+0.010864030.989136
ENST00000540420ENST00000374338RUNX3chr125245730-LDLRAP1chr125880412+0.0048554410.99514455

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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

>78714_78714_1_RUNX3-LDLRAP1_RUNX3_chr1_25245730_ENST00000308873_LDLRAP1_chr1_25880412_ENST00000374338_length(amino acids)=460AA_BP=182
MRIPVDPSTSRRFTPPSPAFPCGGGGGKMGENSGALSAQAAVGPGGRARPEVRSMVDVLADHAGELVRTDSPNFLCSVLPSHWRCNKTLP
VAFKVVALGDVPDGTVVTVMAGNDENYSAELRNASAVMKNQVARFNDLRFVGRSGRGKSFTLTITVFTNPTQVATYHRAIKVTVDGPREP
RQLPENWTDTRETLLEGMLFSLKYLGMTLVEQPKGEELSAAAIKRIVATAKASGKKLQKVTLKVSPRGIILTDNLTNQLIENVSIYRISY
CTADKMHDKVFAYIAQSQHNQSLECHAFLCTKRKMAQAVTLTVAQAFKVAFEFWQVSKEEKEKRDKASQEGGDVLGARQDCTPSLKSLVA
TGNLLDLEETAKAPLSTVSANTTNMDEVPRPQALSGSSVVWELDDGLDEAFSRLAQSRTNPQVLDTGLTAQDMHYAQCLSPVDWDKPDSS

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

>78714_78714_2_RUNX3-LDLRAP1_RUNX3_chr1_25245730_ENST00000399916_LDLRAP1_chr1_25880412_ENST00000374338_length(amino acids)=474AA_BP=196
MASNSIFDSFPTYSPTFIRDPSTSRRFTPPSPAFPCGGGGGKMGENSGALSAQAAVGPGGRARPEVRSMVDVLADHAGELVRTDSPNFLC
SVLPSHWRCNKTLPVAFKVVALGDVPDGTVVTVMAGNDENYSAELRNASAVMKNQVARFNDLRFVGRSGRGKSFTLTITVFTNPTQVATY
HRAIKVTVDGPREPRQLPENWTDTRETLLEGMLFSLKYLGMTLVEQPKGEELSAAAIKRIVATAKASGKKLQKVTLKVSPRGIILTDNLT
NQLIENVSIYRISYCTADKMHDKVFAYIAQSQHNQSLECHAFLCTKRKMAQAVTLTVAQAFKVAFEFWQVSKEEKEKRDKASQEGGDVLG
ARQDCTPSLKSLVATGNLLDLEETAKAPLSTVSANTTNMDEVPRPQALSGSSVVWELDDGLDEAFSRLAQSRTNPQVLDTGLTAQDMHYA

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

>78714_78714_3_RUNX3-LDLRAP1_RUNX3_chr1_25245730_ENST00000540420_LDLRAP1_chr1_25880412_ENST00000374338_length(amino acids)=367AA_BP=89
MVVALGDVPDGTVVTVMAGNDENYSAELRNASAVMKNQVARFNDLRFVGRSGRGKSFTLTITVFTNPTQVATYHRAIKVTVDGPREPRQL
PENWTDTRETLLEGMLFSLKYLGMTLVEQPKGEELSAAAIKRIVATAKASGKKLQKVTLKVSPRGIILTDNLTNQLIENVSIYRISYCTA
DKMHDKVFAYIAQSQHNQSLECHAFLCTKRKMAQAVTLTVAQAFKVAFEFWQVSKEEKEKRDKASQEGGDVLGARQDCTPSLKSLVATGN
LLDLEETAKAPLSTVSANTTNMDEVPRPQALSGSSVVWELDDGLDEAFSRLAQSRTNPQVLDTGLTAQDMHYAQCLSPVDWDKPDSSGTE

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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/chr1:25245730/chr1:25880412)
- 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
.LDLRAP1

Q5SW96

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: Adapter protein (clathrin-associated sorting protein (CLASP)) required for efficient endocytosis of the LDL receptor (LDLR) in polarized cells such as hepatocytes and lymphocytes, but not in non-polarized cells (fibroblasts). May be required for LDL binding and internalization but not for receptor clustering in coated pits. May facilitate the endocytocis of LDLR and LDLR-LDL complexes from coated pits by stabilizing the interaction between the receptor and the structural components of the pits. May also be involved in the internalization of other LDLR family members. Binds to phosphoinositides, which regulate clathrin bud assembly at the cell surface. Required for trafficking of LRP2 to the endocytic recycling compartment which is necessary for LRP2 proteolysis, releasing a tail fragment which translocates to the nucleus and mediates transcriptional repression (By similarity). {ECO:0000250|UniProtKB:D3ZAR1, ECO:0000269|PubMed:15728179}.

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
HgeneRUNX3chr1:25245730chr1:25880412ENST00000308873-3523_27181.33333333333334416.0Compositional biasNote=Poly-Gly
HgeneRUNX3chr1:25245730chr1:25880412ENST00000338888-5723_27195.33333333333334430.0Compositional biasNote=Poly-Gly
HgeneRUNX3chr1:25245730chr1:25880412ENST00000399916-4623_27195.33333333333334430.0Compositional biasNote=Poly-Gly
HgeneRUNX3chr1:25245730chr1:25880412ENST00000308873-3554_182181.33333333333334416.0DomainRunt
HgeneRUNX3chr1:25245730chr1:25880412ENST00000338888-5754_182195.33333333333334430.0DomainRunt
HgeneRUNX3chr1:25245730chr1:25880412ENST00000399916-4654_182195.33333333333334430.0DomainRunt
TgeneLDLRAP1chr1:25245730chr1:25880412ENST000003743380942_19629.333333333333332309.0DomainPID
TgeneLDLRAP1chr1:25245730chr1:25880412ENST0000037433809212_21629.333333333333332309.0MotifClathrin box
TgeneLDLRAP1chr1:25245730chr1:25880412ENST0000037433809257_26629.333333333333332309.0Motif[DE]-X(1%2C2)-F-X-X-[FL]-X-X-X-R motif
TgeneLDLRAP1chr1:25245730chr1:25880412ENST0000037433809249_27629.333333333333332309.0RegionAP-2 complex binding

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRUNX3chr1:25245730chr1:25880412ENST00000308873-35191_415181.33333333333334416.0Compositional biasNote=Pro/Ser/Thr-rich
HgeneRUNX3chr1:25245730chr1:25880412ENST00000338888-57191_415195.33333333333334430.0Compositional biasNote=Pro/Ser/Thr-rich
HgeneRUNX3chr1:25245730chr1:25880412ENST00000399916-46191_415195.33333333333334430.0Compositional biasNote=Pro/Ser/Thr-rich
TgeneLDLRAP1chr1:25245730chr1:25880412ENST000003743380923_2629.333333333333332309.0Compositional biasNote=Poly-Gly


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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
RUNX3
LDLRAP1


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 RUNX3-LDLRAP1


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 RUNX3-LDLRAP1


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