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Fusion gene ID: 15571 |
FusionGeneSummary for GSPT1_HPGD |
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Fusion gene information | Fusion gene name: GSPT1_HPGD | Fusion gene ID: 15571 | Hgene | Tgene | Gene symbol | GSPT1 | HPGD | Gene ID | 2935 | 3248 |
Gene name | G1 to S phase transition 1 | 15-hydroxyprostaglandin dehydrogenase | |
Synonyms | 551G9.2|ETF3A|GST1|eRF3a | 15-PGDH|PGDH|PGDH1|PHOAR1|SDR36C1 | |
Cytomap | 16p13.13 | 4q34.1 | |
Type of gene | protein-coding | protein-coding | |
Description | eukaryotic peptide chain release factor GTP-binding subunit ERF3AG1 to S phase transition protein 1 homologeukaryotic peptide chain release factor subunit 3aeukaryotic release factor 3a | 15-hydroxyprostaglandin dehydrogenase [NAD(+)]15-hydroxyprostaglandin dehydrogenase (NAD(+))NAD+-dependent 15-hydroxyprostaglandin dehydrogenasehydroxyprostaglandin dehydrogenase 15-(NAD)prostaglandin dehydrogenase 1short chain dehydrogenase/reductas | |
Modification date | 20180523 | 20180524 | |
UniProtAcc | P15170 | P15428 | |
Ensembl transtripts involved in fusion gene | ENST00000434724, ENST00000439887, ENST00000563468, ENST00000420576, ENST00000564790, | ENST00000296522, ENST00000296521, ENST00000510901, ENST00000422112, ENST00000541923, ENST00000542498, ENST00000504433, | |
Fusion gene scores | * DoF score | 2 X 2 X 1=4 | 3 X 3 X 2=18 |
# samples | 2 | 3 | |
** MAII score | log2(2/4*10)=2.32192809488736 | log2(3/18*10)=0.736965594166206 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: GSPT1 [Title/Abstract] AND HPGD [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 |
Hgene | GSPT1 | GO:0006479 | protein methylation | 18539146 |
Tgene | HPGD | GO:0006693 | prostaglandin metabolic process | 16828555 |
Tgene | HPGD | GO:0007179 | transforming growth factor beta receptor signaling pathway | 15574495 |
Tgene | HPGD | GO:0007565 | female pregnancy | 15531523 |
Tgene | HPGD | GO:0007567 | parturition | 15531523 |
Tgene | HPGD | GO:0045786 | negative regulation of cell cycle | 15574495 |
![]() (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 | BF736330 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
* 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-3CDS | ENST00000434724 | ENST00000296522 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-3CDS | ENST00000434724 | ENST00000296521 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000434724 | ENST00000510901 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000434724 | ENST00000422112 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000434724 | ENST00000541923 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000434724 | ENST00000542498 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000434724 | ENST00000504433 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-3CDS | ENST00000439887 | ENST00000296522 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-3CDS | ENST00000439887 | ENST00000296521 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000439887 | ENST00000510901 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000439887 | ENST00000422112 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000439887 | ENST00000541923 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000439887 | ENST00000542498 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000439887 | ENST00000504433 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-3CDS | ENST00000563468 | ENST00000296522 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-3CDS | ENST00000563468 | ENST00000296521 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000563468 | ENST00000510901 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000563468 | ENST00000422112 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000563468 | ENST00000541923 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000563468 | ENST00000542498 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000563468 | ENST00000504433 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-3CDS | ENST00000420576 | ENST00000296522 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-3CDS | ENST00000420576 | ENST00000296521 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000420576 | ENST00000510901 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000420576 | ENST00000422112 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000420576 | ENST00000541923 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000420576 | ENST00000542498 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000420576 | ENST00000504433 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-3CDS | ENST00000564790 | ENST00000296522 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-3CDS | ENST00000564790 | ENST00000296521 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000564790 | ENST00000510901 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000564790 | ENST00000422112 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000564790 | ENST00000541923 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000564790 | ENST00000542498 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
intron-5UTR | ENST00000564790 | ENST00000504433 | GSPT1 | chr16 | 11991740 | + | HPGD | chr4 | 175443155 | - |
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FusionProtFeatures for GSPT1_HPGD |
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Hgene | Tgene |
GSPT1 | HPGD |
Involved in translation termination in response to thetermination codons UAA, UAG and UGA. Stimulates the activity ofERF1. Involved in regulation of mammalian cell growth. Componentof the transient SURF complex which recruits UPF1 to stalledribosomes in the context of nonsense-mediated decay (NMD) of mRNAscontaining premature stop codons. |
![]() * 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 GSPT1_HPGD |
![]() (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 GSPT1_HPGD |
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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 GSPT1_HPGD |
![]() (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 GSPT1_HPGD |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | HPGD | C0029411 | Osteoarthropathy, Primary Hypertrophic | 2 | CTD_human;ORPHANET;UNIPROT |
Tgene | HPGD | C0033578 | Prostatic Neoplasms | 1 | CTD_human |
Tgene | HPGD | C0040136 | Thyroid Neoplasm | 1 | CTD_human |
Tgene | HPGD | C0206693 | Medullary carcinoma | 1 | CTD_human |
Tgene | HPGD | C0345408 | Hereditary clubbing | 1 | ORPHANET;UNIPROT |