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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: 25579

FusionGeneSummary for OSBPL9_C1orf87

check button Fusion gene summary
Fusion gene informationFusion gene name: OSBPL9_C1orf87
Fusion gene ID: 25579
HgeneTgene
Gene symbol

OSBPL9

C1orf87

Gene ID

114883

127795

Gene nameoxysterol binding protein like 9chromosome 1 open reading frame 87
SynonymsORP-9|ORP9CREF
Cytomap

1p32.3

1p32.1

Type of geneprotein-codingprotein-coding
Descriptionoxysterol-binding protein-related protein 9OSBP-related protein 9uncharacterized protein C1orf87carcinoma-related EF-hand protein
Modification date2018052320180519
UniProtAcc

Q96SU4

Q8N0U7

Ensembl transtripts involved in fusion geneENST00000371714, ENST00000371710, 
ENST00000337809, ENST00000435686, 
ENST00000447887, ENST00000453295, 
ENST00000428468, ENST00000530544, 
ENST00000531828, ENST00000361556, 
ENST00000473207, ENST00000462759, 
ENST00000486942, 
ENST00000486478, 
ENST00000450089, ENST00000371201, 
ENST00000395552, 
Fusion gene scores* DoF score10 X 8 X 6=4805 X 5 X 5=125
# samples 125
** MAII scorelog2(12/480*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/125*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: OSBPL9 [Title/Abstract] AND C1orf87 [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
TCGARVBRCATCGA-E9-A1R7-01AOSBPL9chr1

52117713

+C1orf87chr1

60476128

-
* 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-intronENST00000371714ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000371714ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000371714ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000371714ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000371710ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000371710ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000371710ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000371710ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000337809ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000337809ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000337809ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000337809ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5UTR-intronENST00000435686ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5UTR-intronENST00000435686ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5UTR-intronENST00000435686ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5UTR-intronENST00000435686ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000447887ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000447887ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000447887ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000447887ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000453295ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000453295ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000453295ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000453295ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000428468ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000428468ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000428468ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
5CDS-intronENST00000428468ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000530544ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000530544ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000530544ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000530544ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000531828ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000531828ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000531828ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000531828ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000361556ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000361556ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000361556ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000361556ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000473207ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000473207ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000473207ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000473207ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000462759ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000462759ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000462759ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000462759ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000486942ENST00000486478OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000486942ENST00000450089OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000486942ENST00000371201OSBPL9chr1

52117713

+C1orf87chr1

60476128

-
intron-intronENST00000486942ENST00000395552OSBPL9chr1

52117713

+C1orf87chr1

60476128

-

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FusionProtFeatures for OSBPL9_C1orf87


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
OSBPL9

Q96SU4

C1orf87

Q8N0U7


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 OSBPL9_C1orf87


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 OSBPL9_C1orf87


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
OSBPL9GCH1, HIST1H2BL, VAPB, VAPA, WRAP73, DTNBP1, KBTBD6, USP11, OSBPL10, OSBPL11, HAUS1, BLOC1S2, TERF2, DNAJA1, CYP1A1, HSPB1, COPE, POLD2, NTRK1, KRAS, CHMP4B, FUZ, CFAP36C1orf87APP, SNX5, SNX1, CDK5RAP2, SNX2, HEPACAM, SARM1, PCNT, MINPP1, AKAP9, HERC1, PDE4DIP, PPM1B, UBR4, PPP2R2D, FKBP15


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 OSBPL9_C1orf87


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 OSBPL9_C1orf87


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