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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 18658

FusionGeneSummary for KIAA1191_MYO9B

check button Fusion gene summary
Fusion gene informationFusion gene name: KIAA1191_MYO9B
Fusion gene ID: 18658
HgeneTgene
Gene symbol

KIAA1191

MYO9B

Gene ID

57179

4650

Gene nameKIAA1191myosin IXB
Synonymsp33MONOX|p60MONOXCELIAC4|MYR5
Cytomap

5q35.2

19p13.11

Type of geneprotein-codingprotein-coding
Descriptionputative monooxygenase p33MONOXbrain-derived rescue factor p60MONOXflavin monooxygenase motif-containing protein of 33 kDaflavine monooxygenase motif-containing protein of 33 kDap60MONOX brain-derived rescue factorunconventional myosin-IXbmyosin-IXbunconventional myosin-9b
Modification date2018051920180519
UniProtAcc

Q96A73

Q13459

Ensembl transtripts involved in fusion geneENST00000298569, ENST00000393728, 
ENST00000393725, ENST00000510164, 
ENST00000533553, 
ENST00000595618, 
ENST00000594824, ENST00000397274, 
ENST00000593411, 
Fusion gene scores* DoF score5 X 4 X 4=8013 X 14 X 7=1274
# samples 514
** MAII scorelog2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(14/1274*10)=-3.18586654531133
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KIAA1191 [Title/Abstract] AND MYO9B [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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
TgeneMYO9B

GO:0030048

actin filament-based movement

9490638

TgeneMYO9B

GO:0032011

ARF protein signal transduction

15644318

TgeneMYO9B

GO:0035385

Roundabout signaling pathway

26529257


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1BF527288KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-intronENST00000298569ENST00000595618KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000298569ENST00000594824KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000298569ENST00000397274KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000298569ENST00000593411KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000393728ENST00000595618KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000393728ENST00000594824KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000393728ENST00000397274KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000393728ENST00000593411KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000393725ENST00000595618KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000393725ENST00000594824KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000393725ENST00000397274KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000393725ENST00000593411KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000510164ENST00000595618KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000510164ENST00000594824KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000510164ENST00000397274KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000510164ENST00000593411KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000533553ENST00000595618KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000533553ENST00000594824KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000533553ENST00000397274KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-
intron-intronENST00000533553ENST00000593411KIAA1191chr5

175774401

-MYO9Bchr19

17243205

-

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FusionProtFeatures for KIAA1191_MYO9B


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
KIAA1191

Q96A73

MYO9B

Q13459

Potential NADPH-dependent oxidoreductase. May beinvolved in the regulation of neuronal survival, differentiationand axonal outgrowth. Myosins are actin-based motor molecules with ATPaseactivity. Unconventional myosins serve in intracellular movements.Binds actin with high affinity both in the absence and presence ofATP and its mechanochemical activity is inhibited by calcium ions(PubMed:9490638). Also acts as a GTPase activator for RHOA(PubMed:9490638, PubMed:26529257). Plays a role in the regulationof cell migration via its role as RHOA GTPase activator. This isregulated by its interaction with the SLIT2 receptor ROBO1;interaction with ROBO1 impairs interaction with RHOA andsubsequent activation of RHOA GTPase activity, and thereby leadsto increased levels of active, GTP-bound RHOA (PubMed:26529257).{ECO:0000269|PubMed:26529257, ECO:0000269|PubMed:9490638}.

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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FusionGeneSequence for KIAA1191_MYO9B


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for KIAA1191_MYO9B


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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RelatedDrugs for KIAA1191_MYO9B


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for KIAA1191_MYO9B


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMYO9BC0036341Schizophrenia3PSYGENET