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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:ATP13A3-IQCG

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: ATP13A3-IQCG
FusionPDB ID: 7766
FusionGDB2.0 ID: 7766
HgeneTgene
Gene symbol

ATP13A3

IQCG

Gene ID

79572

84223

Gene nameATPase 13A3IQ motif containing G
SynonymsAFURS1CFAP122|DRC9
Cytomap

3q29

3q29

Type of geneprotein-codingprotein-coding
Descriptionprobable cation-transporting ATPase 13A3ATPase family homolog up-regulated in senescence cells 1ATPase type 13A3dynein regulatory complex protein 9IQ domain-containing protein Gdynein regulatory complex subunit 9
Modification date2020031320200313
UniProtAcc

Q9H7F0

Q9H095

Ensembl transtripts involved in fusion geneENST idsENST00000256031, ENST00000439040, 
ENST00000453254, ENST00000480302, 
ENST00000265239, ENST00000455191, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 10 X 5=35012 X 7 X 6=504
# samples 1212
** MAII scorelog2(12/350*10)=-1.54432051622381
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/504*10)=-2.0703893278914
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: ATP13A3 [Title/Abstract] AND IQCG [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)ATP13A3(194170874)-IQCG(197619630), # samples:2
Anticipated loss of major functional domain due to fusion event.ATP13A3-IQCG 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.
ATP13A3-IQCG 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.
ATP13A3-IQCG seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ATP13A3-IQCG seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target 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 ATP13A3 (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 IQCG (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-24-2023-01AATP13A3chr3

194170874

-IQCGchr3

197619630

-


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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)
ENST00000256031ATP13A3chr3194170874-ENST00000265239IQCGchr3197619630-224613724021379325
ENST00000256031ATP13A3chr3194170874-ENST00000455191IQCGchr3197619630-224413724021379325

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
ENST00000256031ENST00000265239ATP13A3chr3194170874-IQCGchr3197619630-0.0010861490.9989139
ENST00000256031ENST00000455191ATP13A3chr3194170874-IQCGchr3197619630-0.0010808960.9989191

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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

>7766_7766_1_ATP13A3-IQCG_ATP13A3_chr3_194170874_ENST00000256031_IQCG_chr3_197619630_ENST00000265239_length(amino acids)=325AA_BP=
MDREERKTINQGQEDEMEIYGYNLSRWKLAIVSLGVICSGGFLLLLLYWMPEWRVKATCVRAAIKDCEVVLLRTTDEFKMWFCAKIRVLS
LETYPVSSPKSMSNKLSNGHAVCLIENPTEENRHRISKYSQTESQQIRYFTHHSVKYFWNDTIHNFDFLKGLDEGVSCTSIYEKHSAGLT
KGMHAYRKLLYGVNEIAVKVPSVFKLLIKEVLNPFYIFQLFSVILWSTDEYYYYALAIVVMSIVSIVSSLYSIRKQYVMLHDMVATHSTV

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

>7766_7766_2_ATP13A3-IQCG_ATP13A3_chr3_194170874_ENST00000256031_IQCG_chr3_197619630_ENST00000455191_length(amino acids)=325AA_BP=
MDREERKTINQGQEDEMEIYGYNLSRWKLAIVSLGVICSGGFLLLLLYWMPEWRVKATCVRAAIKDCEVVLLRTTDEFKMWFCAKIRVLS
LETYPVSSPKSMSNKLSNGHAVCLIENPTEENRHRISKYSQTESQQIRYFTHHSVKYFWNDTIHNFDFLKGLDEGVSCTSIYEKHSAGLT
KGMHAYRKLLYGVNEIAVKVPSVFKLLIKEVLNPFYIFQLFSVILWSTDEYYYYALAIVVMSIVSIVSSLYSIRKQYVMLHDMVATHSTV

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

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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/chr3:194170874/chr3:197619630)
- 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
ATP13A3

Q9H7F0

IQCG

Q9H095

FUNCTION: Component of the nexin-dynein regulatory complex (N-DRC), a key regulator of ciliary/flagellar motility which maintains the alignment and integrity of the distal axoneme and regulates microtubule sliding in motile axonemes. Binds calmodulin when cellular Ca(2+) levels are low and thereby contributes to the regulation of calcium and calmodulin-dependent protein kinase IV (CAMK4) activity; contributes to the regulation of CAMK4 signaling cascades. Required for normal axoneme assembly in sperm flagella, normal sperm tail formation and for male fertility. {ECO:0000250|UniProtKB:A3KQH2, ECO:0000250|UniProtKB:A8HQ54, ECO:0000250|UniProtKB:Q80W32}.

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
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-1032231_234323.33333333333331227.0Compositional biasNote=Poly-Tyr
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-1133231_234323.33333333333331227.0Compositional biasNote=Poly-Tyr
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-1032206_226323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-1032233_253323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-103229_49323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-1133206_226323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-1133233_253323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-113329_49323.33333333333331227.0TransmembraneHelical
TgeneIQCGchr3:194170874chr3:197619630ENST00000265239812393_422321.0444.0DomainIQ
TgeneIQCGchr3:194170874chr3:197619630ENST00000455191711393_422321.0444.0DomainIQ

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-10321000_1020323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-10321074_1094323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-10321106_1126323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-10321144_1164323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-1032410_430323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-1032449_469323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-1032941_961323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000256031-1032963_983323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-11331000_1020323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-11331074_1094323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-11331106_1126323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-11331144_1164323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-1133410_430323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-1133449_469323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-1133941_961323.33333333333331227.0TransmembraneHelical
HgeneATP13A3chr3:194170874chr3:197619630ENST00000439040-1133963_983323.33333333333331227.0TransmembraneHelical


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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
ATP13A3
IQCG


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 ATP13A3-IQCG


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 ATP13A3-IQCG


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