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Fusion gene ID: 37936 |
FusionGeneSummary for TGOLN2_TGOLN2 |
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Fusion gene information | Fusion gene name: TGOLN2_TGOLN2 | Fusion gene ID: 37936 | Hgene | Tgene | Gene symbol | TGOLN2 | TGOLN2 | Gene ID | 10618 | 10618 |
Gene name | trans-golgi network protein 2 | trans-golgi network protein 2 | |
Synonyms | TGN38|TGN46|TGN48|TGN51|TTGN2 | TGN38|TGN46|TGN48|TGN51|TTGN2 | |
Cytomap | 2p11.2 | 2p11.2 | |
Type of gene | protein-coding | protein-coding | |
Description | trans-Golgi network integral membrane protein 2TGN38 homologtrans-Golgi network protein (46, 48, 51kD isoforms)trans-Golgi network protein TGN51 | trans-Golgi network integral membrane protein 2TGN38 homologtrans-Golgi network protein (46, 48, 51kD isoforms)trans-Golgi network protein TGN51 | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | O43493 | O43493 | |
Ensembl transtripts involved in fusion gene | ENST00000282120, ENST00000377386, ENST00000398263, ENST00000409232, ENST00000409015, ENST00000444342, | ENST00000282120, ENST00000377386, ENST00000398263, ENST00000409232, ENST00000409015, ENST00000444342, | |
Fusion gene scores | * DoF score | 7 X 7 X 3=147 | 8 X 8 X 1=64 |
# samples | 7 | 8 | |
** MAII score | log2(7/147*10)=-1.0703893278914 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(8/64*10)=0.321928094887362 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: TGOLN2 [Title/Abstract] AND TGOLN2 [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 | BE933259 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
* 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-3UTR | ENST00000282120 | ENST00000282120 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000282120 | ENST00000377386 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000282120 | ENST00000398263 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000282120 | ENST00000409232 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000282120 | ENST00000409015 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-intron | ENST00000282120 | ENST00000444342 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000377386 | ENST00000282120 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000377386 | ENST00000377386 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000377386 | ENST00000398263 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000377386 | ENST00000409232 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000377386 | ENST00000409015 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-intron | ENST00000377386 | ENST00000444342 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000398263 | ENST00000282120 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000398263 | ENST00000377386 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000398263 | ENST00000398263 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000398263 | ENST00000409232 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000398263 | ENST00000409015 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-intron | ENST00000398263 | ENST00000444342 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000409232 | ENST00000282120 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000409232 | ENST00000377386 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000409232 | ENST00000398263 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000409232 | ENST00000409232 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000409232 | ENST00000409015 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-intron | ENST00000409232 | ENST00000444342 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000409015 | ENST00000282120 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000409015 | ENST00000377386 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000409015 | ENST00000398263 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000409015 | ENST00000409232 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000409015 | ENST00000409015 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-intron | ENST00000409015 | ENST00000444342 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000444342 | ENST00000282120 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000444342 | ENST00000377386 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000444342 | ENST00000398263 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000444342 | ENST00000409232 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-3UTR | ENST00000444342 | ENST00000409015 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
intron-intron | ENST00000444342 | ENST00000444342 | TGOLN2 | chr2 | 85549344 | - | TGOLN2 | chr2 | 85549479 | + |
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FusionProtFeatures for TGOLN2_TGOLN2 |
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Hgene | Tgene |
TGOLN2 | TGOLN2 |
![]() * 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 TGOLN2_TGOLN2 |
![]() (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 TGOLN2_TGOLN2 |
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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 TGOLN2_TGOLN2 |
![]() (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 TGOLN2_TGOLN2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | TGOLN2 | C0040128 | Thyroid Diseases | 1 | CTD_human |
Hgene | TGOLN2 | C0525045 | Mood Disorders | 1 | PSYGENET |
Tgene | TGOLN2 | C0040128 | Thyroid Diseases | 1 | CTD_human |
Tgene | TGOLN2 | C0525045 | Mood Disorders | 1 | PSYGENET |