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Fusion gene ID: 27655 |
FusionGeneSummary for PLEKHH2_VSNL1 |
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Fusion gene information | Fusion gene name: PLEKHH2_VSNL1 | Fusion gene ID: 27655 | Hgene | Tgene | Gene symbol | PLEKHH2 | VSNL1 | Gene ID | 130271 | 7447 |
Gene name | pleckstrin homology, MyTH4 and FERM domain containing H2 | visinin like 1 | |
Synonyms | PLEKHH1L | HLP3|HPCAL3|HUVISL1|VILIP|VILIP-1 | |
Cytomap | 2p21 | 2p24.2 | |
Type of gene | protein-coding | protein-coding | |
Description | pleckstrin homology domain-containing family H member 2pleckstrin homology domain containing, family H (with MyTH4 domain) member 2 | visinin-like protein 1VLP-1hippocalcin-like protein 3 | |
Modification date | 20180519 | 20180519 | |
UniProtAcc | Q8IVE3 | P62760 | |
Ensembl transtripts involved in fusion gene | ENST00000282406, | ENST00000404666, ENST00000295156, ENST00000406397, ENST00000483921, | |
Fusion gene scores | * DoF score | 3 X 2 X 3=18 | 3 X 4 X 3=36 |
# samples | 3 | 4 | |
** MAII score | log2(3/18*10)=0.736965594166206 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(4/36*10)=0.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: PLEKHH2 [Title/Abstract] AND VSNL1 [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 |
TCGA | RV | PRAD | TCGA-HC-8262-01A | PLEKHH2 | chr2 | 43871935 | + | VSNL1 | chr2 | 17773337 | + |
TCGA | LD | PRAD | TCGA-HC-8262-01A | PLEKHH2 | chr2 | 43871935 | + | VSNL1 | chr2 | 17748647 | + |
* 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 |
5CDS-5UTR | ENST00000282406 | ENST00000404666 | PLEKHH2 | chr2 | 43871935 | + | VSNL1 | chr2 | 17773337 | + |
5CDS-5UTR | ENST00000282406 | ENST00000295156 | PLEKHH2 | chr2 | 43871935 | + | VSNL1 | chr2 | 17773337 | + |
5CDS-5UTR | ENST00000282406 | ENST00000406397 | PLEKHH2 | chr2 | 43871935 | + | VSNL1 | chr2 | 17773337 | + |
5CDS-intron | ENST00000282406 | ENST00000483921 | PLEKHH2 | chr2 | 43871935 | + | VSNL1 | chr2 | 17773337 | + |
5CDS-intron | ENST00000282406 | ENST00000404666 | PLEKHH2 | chr2 | 43871935 | + | VSNL1 | chr2 | 17748647 | + |
5CDS-intron | ENST00000282406 | ENST00000295156 | PLEKHH2 | chr2 | 43871935 | + | VSNL1 | chr2 | 17748647 | + |
5CDS-intron | ENST00000282406 | ENST00000406397 | PLEKHH2 | chr2 | 43871935 | + | VSNL1 | chr2 | 17748647 | + |
5CDS-3UTR | ENST00000282406 | ENST00000483921 | PLEKHH2 | chr2 | 43871935 | + | VSNL1 | chr2 | 17748647 | + |
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FusionProtFeatures for PLEKHH2_VSNL1 |
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Hgene | Tgene |
PLEKHH2 | VSNL1 |
In the kidney glomerulus may play a role in linkingpodocyte foot processes to the glomerular basement membrane. Maybe involved in stabilization of F-actin by attenuating itsdepolymerization. Can recruit TGFB1I1 from focal adhesions topodocyte lamellipodia. | 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 PLEKHH2_VSNL1 |
![]() (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 PLEKHH2_VSNL1 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
PLEKHH2 | LYN, LPXN, FBXW11 | VSNL1 | DTX2, FAM131C, ATXN1, GFI1B, ARMC1, HAX1, NUFIP1, CDCA8, DGUOK, DNAAF2 |
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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 PLEKHH2_VSNL1 |
![]() (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 PLEKHH2_VSNL1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | VSNL1 | C0036341 | Schizophrenia | 2 | PSYGENET |
Tgene | VSNL1 | C0002395 | Alzheimer's Disease | 1 | CTD_human |