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Fusion gene ID: 12203 |
FusionGeneSummary for EVC2_HDAC7 |
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Fusion gene information | Fusion gene name: EVC2_HDAC7 | Fusion gene ID: 12203 | Hgene | Tgene | Gene symbol | EVC2 | HDAC7 | Gene ID | 132884 | 51564 |
Gene name | EvC ciliary complex subunit 2 | histone deacetylase 7 | |
Synonyms | LBN|WAD | HD7|HD7A|HDAC7A | |
Cytomap | 4p16.2 | 12q13.11 | |
Type of gene | protein-coding | protein-coding | |
Description | limbinEllis van Creveld syndrome 2ellis-van Creveld syndrome protein 2 | histone deacetylase 7histone deacetylase 7A | |
Modification date | 20180519 | 20180522 | |
UniProtAcc | Q86UK5 | Q8WUI4 | |
Ensembl transtripts involved in fusion gene | ENST00000344938, ENST00000344408, ENST00000310917, | ENST00000080059, ENST00000354334, ENST00000552960, ENST00000380610, ENST00000427332, ENST00000488927, | |
Fusion gene scores | * DoF score | 4 X 4 X 3=48 | 6 X 5 X 4=120 |
# samples | 4 | 6 | |
** MAII score | log2(4/48*10)=-0.263034405833794 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(6/120*10)=-1 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: EVC2 [Title/Abstract] AND HDAC7 [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 |
Tgene | HDAC7 | GO:0032703 | negative regulation of interleukin-2 production | 17360565 |
![]() (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 | AI671208 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
* 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 |
intron-intron | ENST00000344938 | ENST00000080059 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344938 | ENST00000354334 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344938 | ENST00000552960 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344938 | ENST00000380610 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344938 | ENST00000427332 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344938 | ENST00000488927 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344408 | ENST00000080059 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344408 | ENST00000354334 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344408 | ENST00000552960 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344408 | ENST00000380610 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344408 | ENST00000427332 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000344408 | ENST00000488927 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000310917 | ENST00000080059 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000310917 | ENST00000354334 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000310917 | ENST00000552960 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000310917 | ENST00000380610 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000310917 | ENST00000427332 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
intron-intron | ENST00000310917 | ENST00000488927 | EVC2 | chr4 | 5630921 | - | HDAC7 | chr12 | 48185223 | + |
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FusionProtFeatures for EVC2_HDAC7 |
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Hgene | Tgene |
EVC2 | HDAC7 |
Component of the EvC complex that positively regulatesciliary Hedgehog (Hh) signaling. Plays a critical role in boneformation and skeletal development. May be involved in earlyembryonic morphogenesis. {ECO:0000250|UniProtKB:Q8K1G2}. |
![]() * 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 EVC2_HDAC7 |
![]() (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 EVC2_HDAC7 |
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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 EVC2_HDAC7 |
![]() (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 EVC2_HDAC7 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | EVC2 | C0013903 | Ellis-Van Creveld Syndrome | 2 | CTD_human;ORPHANET;UNIPROT |