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Fusion gene ID: 41672 |
FusionGeneSummary for VSNL1_BTBD9 |
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Fusion gene information | Fusion gene name: VSNL1_BTBD9 | Fusion gene ID: 41672 | Hgene | Tgene | Gene symbol | VSNL1 | BTBD9 | Gene ID | 7447 | 114781 |
Gene name | visinin like 1 | BTB domain containing 9 | |
Synonyms | HLP3|HPCAL3|HUVISL1|VILIP|VILIP-1 | dJ322I12.1 | |
Cytomap | 2p24.2 | 6p21.2 | |
Type of gene | protein-coding | protein-coding | |
Description | visinin-like protein 1VLP-1hippocalcin-like protein 3 | BTB/POZ domain-containing protein 9BTB (POZ) domain containing 9 | |
Modification date | 20180519 | 20180523 | |
UniProtAcc | P62760 | Q96Q07 | |
Ensembl transtripts involved in fusion gene | ENST00000404666, ENST00000295156, ENST00000406397, ENST00000483921, | ENST00000314100, ENST00000481247, ENST00000419706, ENST00000408958, ENST00000403056, | |
Fusion gene scores | * DoF score | 1 X 1 X 1=1 | 7 X 8 X 5=280 |
# samples | 1 | 9 | |
** MAII score | log2(1/1*10)=3.32192809488736 | log2(9/280*10)=-1.63742992061529 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: VSNL1 [Title/Abstract] AND BTBD9 [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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
![]() (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 type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChiTaRS3.1 | DB301956 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
3UTR-3UTR | ENST00000404666 | ENST00000314100 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-3UTR | ENST00000404666 | ENST00000481247 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-intron | ENST00000404666 | ENST00000419706 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-intron | ENST00000404666 | ENST00000408958 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-intron | ENST00000404666 | ENST00000403056 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-3UTR | ENST00000295156 | ENST00000314100 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-3UTR | ENST00000295156 | ENST00000481247 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-intron | ENST00000295156 | ENST00000419706 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-intron | ENST00000295156 | ENST00000408958 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-intron | ENST00000295156 | ENST00000403056 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-3UTR | ENST00000406397 | ENST00000314100 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-3UTR | ENST00000406397 | ENST00000481247 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-intron | ENST00000406397 | ENST00000419706 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-intron | ENST00000406397 | ENST00000408958 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
3UTR-intron | ENST00000406397 | ENST00000403056 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
intron-3UTR | ENST00000483921 | ENST00000314100 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
intron-3UTR | ENST00000483921 | ENST00000481247 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
intron-intron | ENST00000483921 | ENST00000419706 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
intron-intron | ENST00000483921 | ENST00000408958 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
intron-intron | ENST00000483921 | ENST00000403056 | VSNL1 | chr2 | 17836700 | - | BTBD9 | chr6 | 38141711 | + |
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FusionProtFeatures for VSNL1_BTBD9 |
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Hgene | Tgene |
VSNL1 | BTBD9 |
Regulates (in vitro) the inhibition of rhodopsinphosphorylation in a calcium-dependent manner. {ECO:0000250}. |
![]() * 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. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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FusionGeneSequence for VSNL1_BTBD9 |
![]() (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 VSNL1_BTBD9 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for VSNL1_BTBD9 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for VSNL1_BTBD9 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | VSNL1 | C0036341 | Schizophrenia | 2 | PSYGENET |
Hgene | VSNL1 | C0002395 | Alzheimer's Disease | 1 | CTD_human |
Tgene | BTBD9 | C0035258 | Restless Legs Syndrome | 1 | CTD_human |
Tgene | BTBD9 | C0036341 | Schizophrenia | 1 | PSYGENET |