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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:IQCG-DOCK7 (FusionGDB2 ID:39945)

Fusion Gene Summary for IQCG-DOCK7

check button Fusion gene summary
Fusion gene informationFusion gene name: IQCG-DOCK7
Fusion gene ID: 39945
HgeneTgene
Gene symbol

IQCG

DOCK7

Gene ID

84223

85440

Gene nameIQ motif containing Gdedicator of cytokinesis 7
SynonymsCFAP122|DRC9EIEE23|ZIR2
Cytomap

3q29

1p31.3

Type of geneprotein-codingprotein-coding
Descriptiondynein regulatory complex protein 9IQ domain-containing protein Gdynein regulatory complex subunit 9dedicator of cytokinesis protein 7
Modification date2020031320200327
UniProtAcc

Q9H095

Q96N67

Ensembl transtripts involved in fusion geneENST00000265239, ENST00000455191, 
ENST00000453254, ENST00000480302, 
ENST00000251157, ENST00000340370, 
ENST00000489185, ENST00000404627, 
Fusion gene scores* DoF score13 X 13 X 4=6762 X 2 X 2=8
# samples 152
** MAII scorelog2(15/676*10)=-2.1720607457863
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: IQCG [Title/Abstract] AND DOCK7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointIQCG(197677087)-DOCK7(62976292), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
TgeneDOCK7

GO:0090630

activation of GTPase activity

16982419


check buttonFusion gene breakpoints across IQCG (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across DOCK7 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChiTaRS5.0N/ACA775747IQCGchr3

197677087

-DOCK7chr1

62976292

+


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Fusion Gene ORF analysis for IQCG-DOCK7

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
intron-3CDSENST00000265239ENST00000251157IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-3CDSENST00000265239ENST00000340370IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-intronENST00000265239ENST00000489185IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-intronENST00000265239ENST00000404627IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-3CDSENST00000455191ENST00000251157IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-3CDSENST00000455191ENST00000340370IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-intronENST00000455191ENST00000489185IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-intronENST00000455191ENST00000404627IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-3CDSENST00000453254ENST00000251157IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-3CDSENST00000453254ENST00000340370IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-intronENST00000453254ENST00000489185IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-intronENST00000453254ENST00000404627IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-3CDSENST00000480302ENST00000251157IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-3CDSENST00000480302ENST00000340370IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-intronENST00000480302ENST00000489185IQCGchr3

197677087

-DOCK7chr1

62976292

+
intron-intronENST00000480302ENST00000404627IQCGchr3

197677087

-DOCK7chr1

62976292

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

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

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Fusion Genomic Features for IQCG-DOCK7


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for IQCG-DOCK7


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

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

Q9H095

DOCK7

Q96N67

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}.FUNCTION: Functions as a guanine nucleotide exchange factor (GEF), which activates Rac1 and Rac3 Rho small GTPases by exchanging bound GDP for free GTP. Does not have a GEF activity for CDC42. Required for STMN1 'Ser-15' phosphorylation during axon formation and consequently for neuronal polarization (PubMed:16982419). As part of the DISP complex, may regulate the association of septins with actin and thereby regulate the actin cytoskeleton (PubMed:29467281). Has a role in pigmentation (By similarity). Involved in the regulation of cortical neurogenesis through the control of radial glial cells (RGCs) proliferation versus differentiation; negatively regulates the basal-to-apical interkinetic nuclear migration of RGCs by antagonizing the microtubule growth-promoting function of TACC3 (By similarity). {ECO:0000250|UniProtKB:Q8R1A4, ECO:0000269|PubMed:16982419, ECO:0000269|PubMed:29467281}.

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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Fusion Gene Sequence for IQCG-DOCK7


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for IQCG-DOCK7


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


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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Related Drugs for IQCG-DOCK7


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for IQCG-DOCK7


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneDOCK7C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneDOCK7C4014492EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 231CTD_human;GENOMICS_ENGLAND;ORPHANET