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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: 23467

FusionGeneSummary for NAV3_ARHGAP9

check button Fusion gene summary
Fusion gene informationFusion gene name: NAV3_ARHGAP9
Fusion gene ID: 23467
HgeneTgene
Gene symbol

NAV3

ARHGAP9

Gene ID

89795

64333

Gene nameneuron navigator 3Rho GTPase activating protein 9
SynonymsPOMFIL1|STEERIN3|unc53H310C|RGL1
Cytomap

12q21.2

12q13.3

Type of geneprotein-codingprotein-coding
Descriptionneuron navigator 3pore membrane and/or filament interacting like protein 1unc-53 homolog 3rho GTPase-activating protein 9rho-type GTPase-activating protein 9
Modification date2018052320180523
UniProtAcc

Q8IVL0

Q9BRR9

Ensembl transtripts involved in fusion geneENST00000536525, ENST00000397909, 
ENST00000228327, ENST00000266692, 
ENST00000552300, ENST00000541270, 
ENST00000393791, ENST00000356411, 
ENST00000424809, ENST00000393797, 
ENST00000550288, ENST00000430041, 
ENST00000550454, 
Fusion gene scores* DoF score15 X 9 X 3=4054 X 4 X 4=64
# samples 134
** MAII scorelog2(13/405*10)=-1.63941028474353
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: NAV3 [Title/Abstract] AND ARHGAP9 [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

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
TCGALDGBMTCGA-RR-A6KB-01ANAV3chr12

78452895

+ARHGAP9chr12

57873207

-
* 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
5CDS-5UTRENST00000536525ENST00000393791NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000536525ENST00000356411NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000536525ENST00000424809NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000536525ENST00000393797NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000536525ENST00000550288NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-intronENST00000536525ENST00000430041NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-intronENST00000536525ENST00000550454NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000397909ENST00000393791NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000397909ENST00000356411NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000397909ENST00000424809NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000397909ENST00000393797NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000397909ENST00000550288NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-intronENST00000397909ENST00000430041NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-intronENST00000397909ENST00000550454NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000228327ENST00000393791NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000228327ENST00000356411NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000228327ENST00000424809NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000228327ENST00000393797NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000228327ENST00000550288NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-intronENST00000228327ENST00000430041NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-intronENST00000228327ENST00000550454NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000266692ENST00000393791NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000266692ENST00000356411NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000266692ENST00000424809NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000266692ENST00000393797NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-5UTRENST00000266692ENST00000550288NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-intronENST00000266692ENST00000430041NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
5CDS-intronENST00000266692ENST00000550454NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-5UTRENST00000552300ENST00000393791NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-5UTRENST00000552300ENST00000356411NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-5UTRENST00000552300ENST00000424809NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-5UTRENST00000552300ENST00000393797NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-5UTRENST00000552300ENST00000550288NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-intronENST00000552300ENST00000430041NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-intronENST00000552300ENST00000550454NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-5UTRENST00000541270ENST00000393791NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-5UTRENST00000541270ENST00000356411NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-5UTRENST00000541270ENST00000424809NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-5UTRENST00000541270ENST00000393797NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-5UTRENST00000541270ENST00000550288NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-intronENST00000541270ENST00000430041NAV3chr12

78452895

+ARHGAP9chr12

57873207

-
intron-intronENST00000541270ENST00000550454NAV3chr12

78452895

+ARHGAP9chr12

57873207

-

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FusionProtFeatures for NAV3_ARHGAP9


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NAV3

Q8IVL0

ARHGAP9

Q9BRR9

May regulate IL2 production by T-cells. May be involvedin neuron regeneration. {ECO:0000269|PubMed:16166283}. GTPase activator for the Rho-type GTPases by convertingthem to an inactive GDP-bound state. Has a substantial GAPactivity toward CDC42 and RAC1 and less toward RHOA. Has a role inregulating adhesion of hematopoietic cells to the extracellularmatrix. Binds phosphoinositides, and has the highest affinity forphosphatidylinositol 3,4,5-trisphosphate, followed byphosphatidylinositol 3,4-bisphosphate and phosphatidylinositol4,5-bisphosphate. {ECO:0000269|PubMed:11396949}.

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 NAV3_ARHGAP9


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 NAV3_ARHGAP9


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
NAV3APC, TFAP4, MAPRE1, TRIO, KRASARHGAP9RBPMS, FASLG, APP, MAPK1, MAPK14, SMAD9, FHL2, GRB2


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 NAV3_ARHGAP9


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 NAV3_ARHGAP9


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNAV3C0007134Renal Cell Carcinoma1CTD_human
HgeneNAV3C0027412Opioid-Related Disorders1CTD_human
TgeneARHGAP9C0010073Coronary Artery Vasospasm1CTD_human
TgeneARHGAP9C0023893Liver Cirrhosis, Experimental1CTD_human