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Fusion gene ID: 16745 |
FusionGeneSummary for HPGD_HPGD |
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Fusion gene information | Fusion gene name: HPGD_HPGD | Fusion gene ID: 16745 | Hgene | Tgene | Gene symbol | HPGD | HPGD | Gene ID | 3248 | 3248 |
Gene name | 15-hydroxyprostaglandin dehydrogenase | 15-hydroxyprostaglandin dehydrogenase | |
Synonyms | 15-PGDH|PGDH|PGDH1|PHOAR1|SDR36C1 | 15-PGDH|PGDH|PGDH1|PHOAR1|SDR36C1 | |
Cytomap | 4q34.1 | 4q34.1 | |
Type of gene | protein-coding | protein-coding | |
Description | 15-hydroxyprostaglandin dehydrogenase [NAD(+)]15-hydroxyprostaglandin dehydrogenase (NAD(+))NAD+-dependent 15-hydroxyprostaglandin dehydrogenasehydroxyprostaglandin dehydrogenase 15-(NAD)prostaglandin dehydrogenase 1short chain dehydrogenase/reductas | 15-hydroxyprostaglandin dehydrogenase [NAD(+)]15-hydroxyprostaglandin dehydrogenase (NAD(+))NAD+-dependent 15-hydroxyprostaglandin dehydrogenasehydroxyprostaglandin dehydrogenase 15-(NAD)prostaglandin dehydrogenase 1short chain dehydrogenase/reductas | |
Modification date | 20180524 | 20180524 | |
UniProtAcc | P15428 | P15428 | |
Ensembl transtripts involved in fusion gene | ENST00000296522, ENST00000296521, ENST00000510901, ENST00000422112, ENST00000541923, ENST00000542498, ENST00000504433, | ENST00000296522, ENST00000296521, ENST00000510901, ENST00000422112, ENST00000541923, ENST00000542498, ENST00000504433, | |
Fusion gene scores | * DoF score | 2 X 2 X 2=8 | 3 X 3 X 2=18 |
# samples | 2 | 3 | |
** MAII score | log2(2/8*10)=1.32192809488736 | log2(3/18*10)=0.736965594166206 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: HPGD [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 | HPGD | GO:0006693 | prostaglandin metabolic process | 16828555 |
Hgene | HPGD | GO:0007179 | transforming growth factor beta receptor signaling pathway | 15574495 |
Hgene | HPGD | GO:0007565 | female pregnancy | 15531523 |
Hgene | HPGD | GO:0007567 | parturition | 15531523 |
Hgene | HPGD | GO:0045786 | negative regulation of cell cycle | 15574495 |
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 | J05594 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
* 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 | ENST00000296522 | ENST00000296522 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296522 | ENST00000296521 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296522 | ENST00000510901 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296522 | ENST00000422112 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296522 | ENST00000541923 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296522 | ENST00000542498 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296522 | ENST00000504433 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-3UTR | ENST00000296521 | ENST00000296522 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296521 | ENST00000296521 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296521 | ENST00000510901 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296521 | ENST00000422112 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296521 | ENST00000541923 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296521 | ENST00000542498 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000296521 | ENST00000504433 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-3UTR | ENST00000510901 | ENST00000296522 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000510901 | ENST00000296521 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000510901 | ENST00000510901 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000510901 | ENST00000422112 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000510901 | ENST00000541923 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000510901 | ENST00000542498 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000510901 | ENST00000504433 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-3UTR | ENST00000422112 | ENST00000296522 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000422112 | ENST00000296521 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000422112 | ENST00000510901 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000422112 | ENST00000422112 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000422112 | ENST00000541923 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000422112 | ENST00000542498 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000422112 | ENST00000504433 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-3UTR | ENST00000541923 | ENST00000296522 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000541923 | ENST00000296521 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000541923 | ENST00000510901 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000541923 | ENST00000422112 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000541923 | ENST00000541923 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000541923 | ENST00000542498 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000541923 | ENST00000504433 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-3UTR | ENST00000542498 | ENST00000296522 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000542498 | ENST00000296521 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000542498 | ENST00000510901 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000542498 | ENST00000422112 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000542498 | ENST00000541923 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000542498 | ENST00000542498 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000542498 | ENST00000504433 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-3UTR | ENST00000504433 | ENST00000296522 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000504433 | ENST00000296521 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000504433 | ENST00000510901 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000504433 | ENST00000422112 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000504433 | ENST00000541923 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000504433 | ENST00000542498 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
intron-intron | ENST00000504433 | ENST00000504433 | HPGD | chr4 | 175411612 | - | HPGD | chr4 | 175411745 | + |
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FusionProtFeatures for HPGD_HPGD |
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Hgene | Tgene |
HPGD | HPGD |
![]() * 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 HPGD_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 HPGD_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 HPGD_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 HPGD_HPGD |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | HPGD | C0029411 | Osteoarthropathy, Primary Hypertrophic | 2 | CTD_human;ORPHANET;UNIPROT |
Hgene | HPGD | C0033578 | Prostatic Neoplasms | 1 | CTD_human |
Hgene | HPGD | C0040136 | Thyroid Neoplasm | 1 | CTD_human |
Hgene | HPGD | C0206693 | Medullary carcinoma | 1 | CTD_human |
Hgene | HPGD | C0345408 | Hereditary clubbing | 1 | ORPHANET;UNIPROT |
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 |