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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: 2421

FusionGeneSummary for ARHGAP26_OGFOD3

check button Fusion gene summary
Fusion gene informationFusion gene name: ARHGAP26_OGFOD3
Fusion gene ID: 2421
HgeneTgene
Gene symbol

ARHGAP26

OGFOD3

Gene ID

23092

79701

Gene nameRho GTPase activating protein 262-oxoglutarate and iron dependent oxygenase domain containing 3
SynonymsGRAF|GRAF1|OPHN1L|OPHN1L1C17orf101
Cytomap

5q31.3

17q25.3

Type of geneprotein-codingprotein-coding
Descriptionrho GTPase-activating protein 26GTPase regulator associated with focal adhesion kinase pp125(FAK)oligophrenin-1-like protein2-oxoglutarate and iron-dependent oxygenase domain-containing protein 3PKHD domain-containing transmembrane protein C17orf101
Modification date2018052320180519
UniProtAcc

Q9UNA1

Q6PK18

Ensembl transtripts involved in fusion geneENST00000378004, ENST00000274498, 
ENST00000486650, 
ENST00000313056, 
ENST00000329197, ENST00000578287, 
Fusion gene scores* DoF score9 X 12 X 4=4324 X 5 X 5=100
# samples 125
** MAII scorelog2(12/432*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ARHGAP26 [Title/Abstract] AND OGFOD3 [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
ChiTaRS3.1BI045497ARHGAP26chr5

142228861

-OGFOD3chr17

80352348

-
* 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-intronENST00000378004ENST00000313056ARHGAP26chr5

142228861

-OGFOD3chr17

80352348

-
intron-intronENST00000378004ENST00000329197ARHGAP26chr5

142228861

-OGFOD3chr17

80352348

-
intron-intronENST00000378004ENST00000578287ARHGAP26chr5

142228861

-OGFOD3chr17

80352348

-
intron-intronENST00000274498ENST00000313056ARHGAP26chr5

142228861

-OGFOD3chr17

80352348

-
intron-intronENST00000274498ENST00000329197ARHGAP26chr5

142228861

-OGFOD3chr17

80352348

-
intron-intronENST00000274498ENST00000578287ARHGAP26chr5

142228861

-OGFOD3chr17

80352348

-
intron-intronENST00000486650ENST00000313056ARHGAP26chr5

142228861

-OGFOD3chr17

80352348

-
intron-intronENST00000486650ENST00000329197ARHGAP26chr5

142228861

-OGFOD3chr17

80352348

-
intron-intronENST00000486650ENST00000578287ARHGAP26chr5

142228861

-OGFOD3chr17

80352348

-

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FusionProtFeatures for ARHGAP26_OGFOD3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ARHGAP26

Q9UNA1

OGFOD3

Q6PK18

GTPase-activating protein for RHOA and CDC42.

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 ARHGAP26_OGFOD3


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 ARHGAP26_OGFOD3


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 ARHGAP26_OGFOD3


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 ARHGAP26_OGFOD3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneARHGAP26C0033975Psychotic Disorders1PSYGENET
HgeneARHGAP26C0349639Juvenile Myelomonocytic Leukemia1CTD_human;HPO;UNIPROT