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Fusion gene ID: 29306 |
FusionGeneSummary for PTGDS_CLU |
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Fusion gene information | Fusion gene name: PTGDS_CLU | Fusion gene ID: 29306 | Hgene | Tgene | Gene symbol | PTGDS | CLU | Gene ID | 5730 | 1191 |
Gene name | prostaglandin D2 synthase | clusterin | |
Synonyms | L-PGDS|LPGDS|PDS|PGD2|PGDS|PGDS2 | AAG4|APO-J|APOJ|CLI|CLU1|CLU2|KUB1|NA1/NA2|SGP-2|SGP2|SP-40|TRPM-2|TRPM2 | |
Cytomap | 9q34.3 | 8p21.1 | |
Type of gene | protein-coding | protein-coding | |
Description | prostaglandin-H2 D-isomerasePGD2 synthasebeta-trace proteincerebrin-28glutathione-independent PGD synthaseglutathione-independent PGD synthetaselipocalin-type prostaglandin D synthaseprostaglandin D synthaseprostaglandin D2 synthase 21kDa (brain) | clusterinaging-associated protein 4apolipoprotein Jcomplement cytolysis inhibitorcomplement lysis inhibitorcomplement-associated protein SP-40,40ku70-binding protein 1sulfated glycoprotein 2testosterone-repressed prostate message 2 | |
Modification date | 20180519 | 20180527 | |
UniProtAcc | P41222 | P10909 | |
Ensembl transtripts involved in fusion gene | ENST00000224167, ENST00000371625, ENST00000460340, | ENST00000316403, ENST00000546343, ENST00000560366, ENST00000405140, ENST00000523500, | |
Fusion gene scores | * DoF score | 11 X 8 X 3=264 | 14 X 17 X 5=1190 |
# samples | 13 | 18 | |
** MAII score | log2(13/264*10)=-1.02202630633 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(18/1190*10)=-2.72489276186563 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: PTGDS [Title/Abstract] AND CLU [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation | Tumor suppressor gene involved fusion gene, in-frame but not retained their domain. Tumor suppressor gene involved fusion gene, retained protein feature but frameshift. DDR (DNA damage repair) gene involved fusion gene, in-frame but not retained their domain. |
* 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 | PTGDS | GO:0001516 | prostaglandin biosynthetic process | 20667974 |
Tgene | CLU | GO:0000902 | cell morphogenesis | 15857407 |
Tgene | CLU | GO:0001774 | microglial cell activation | 15857407 |
Tgene | CLU | GO:0017038 | protein import | 24446231 |
Tgene | CLU | GO:0032463 | negative regulation of protein homooligomerization | 22179788|23106396 |
Tgene | CLU | GO:0032464 | positive regulation of protein homooligomerization | 22179788 |
Tgene | CLU | GO:0032760 | positive regulation of tumor necrosis factor production | 15857407 |
Tgene | CLU | GO:0045429 | positive regulation of nitric oxide biosynthetic process | 15857407 |
Tgene | CLU | GO:0050821 | protein stabilization | 11123922 |
Tgene | CLU | GO:0051131 | chaperone-mediated protein complex assembly | 17412999 |
Tgene | CLU | GO:0051788 | response to misfolded protein | 19996109 |
Tgene | CLU | GO:0061077 | chaperone-mediated protein folding | 11123922 |
Tgene | CLU | GO:0061518 | microglial cell proliferation | 15857407 |
Tgene | CLU | GO:1900221 | regulation of amyloid-beta clearance | 24446231 |
Tgene | CLU | GO:1901214 | regulation of neuron death | 17412999 |
Tgene | CLU | GO:1901216 | positive regulation of neuron death | 15857407 |
Tgene | CLU | GO:1902430 | negative regulation of amyloid-beta formation | 12047389|17412999 |
Tgene | CLU | GO:1905907 | negative regulation of amyloid fibril formation | 22179788 |
![]() (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 | LD | LGG | TCGA-CS-4944-01A | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
* 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 |
In-frame | ENST00000224167 | ENST00000316403 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
Frame-shift | ENST00000224167 | ENST00000546343 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
Frame-shift | ENST00000224167 | ENST00000560366 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
In-frame | ENST00000224167 | ENST00000405140 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
Frame-shift | ENST00000224167 | ENST00000523500 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
In-frame | ENST00000371625 | ENST00000316403 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
Frame-shift | ENST00000371625 | ENST00000546343 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
Frame-shift | ENST00000371625 | ENST00000560366 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
In-frame | ENST00000371625 | ENST00000405140 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
Frame-shift | ENST00000371625 | ENST00000523500 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
intron-3CDS | ENST00000460340 | ENST00000316403 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
intron-3CDS | ENST00000460340 | ENST00000546343 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
intron-3CDS | ENST00000460340 | ENST00000560366 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
intron-3CDS | ENST00000460340 | ENST00000405140 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
intron-3CDS | ENST00000460340 | ENST00000523500 | PTGDS | chr9 | 139872144 | + | CLU | chr8 | 27455767 | - |
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FusionProtFeatures for PTGDS_CLU |
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Hgene | Tgene |
PTGDS | CLU |
Catalyzes the conversion of PGH2 to PGD2, aprostaglandin involved in smooth muscle contraction/relaxation anda potent inhibitor of platelet aggregation. Involved in a varietyof CNS functions, such as sedation, NREM sleep and PGE2-inducedallodynia, and may have an anti-apoptotic role inoligodendrocytes. Binds small non-substrate lipophilic molecules,including biliverdin, bilirubin, retinal, retinoic acid andthyroid hormone, and may act as a scavenger for harmfulhydrophopic molecules and as a secretory retinoid and thyroidhormone transporter. Possibly involved in development andmaintenance of the blood-brain, blood-retina, blood-aqueous humorand blood-testis barrier. It is likely to play important roles inboth maturation and maintenance of the central nervous system andmale reproductive system. {ECO:0000269|PubMed:20667974,ECO:0000269|PubMed:9475419}. | Isoform 1 functions as extracellular chaperone thatprevents aggregation of nonnative proteins. Prevents stress-induced aggregation of blood plasma proteins. Inhibits formationof amyloid fibrils by APP, APOC2, B2M, CALCA, CSN3, SNCA andaggregation-prone LYZ variants (in vitro). Does not require ATP.Maintains partially unfolded proteins in a state appropriate forsubsequent refolding by other chaperones, such as HSPA8/HSC70.Does not refold proteins by itself. Binding to cell surfacereceptors triggers internalization of the chaperone-client complexand subsequent lysosomal or proteasomal degradation. Secretedisoform 1 protects cells against apoptosis and against cytolysisby complement. Intracellular isoforms interact with ubiquitin andSCF (SKP1-CUL1-F-box protein) E3 ubiquitin-protein ligasecomplexes and promote the ubiquitination and subsequentproteasomal degradation of target proteins. Promotes proteasomaldegradation of COMMD1 and IKBKB. Modulates NF-kappa-Btranscriptional activity. Nuclear isoforms promote apoptosis.Mitochondrial isoforms suppress BAX-dependent release ofcytochrome c into the cytoplasm and inhibit apoptosis. Plays arole in the regulation of cell proliferation.{ECO:0000269|PubMed:11123922, ECO:0000269|PubMed:12047389,ECO:0000269|PubMed:12176985, ECO:0000269|PubMed:12551933,ECO:0000269|PubMed:12882985, ECO:0000269|PubMed:16113678,ECO:0000269|PubMed:17260971, ECO:0000269|PubMed:17407782,ECO:0000269|PubMed:17412999, ECO:0000269|PubMed:17689225,ECO:0000269|PubMed:19137541, ECO:0000269|PubMed:19535339,ECO:0000269|PubMed:19996109, ECO:0000269|PubMed:20068069,ECO:0000269|PubMed:21505792}. |
![]() * 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 |
Tgene | >CLU | chr9:139872144 | chr8:27455767 | ENST00000316403 | - | 7 | 9 | 443_447 | 446 | 450 | Motif | Nuclear localization signal |
Tgene | >CLU | chr9:139872144 | chr8:27455767 | ENST00000405140 | - | 7 | 9 | 443_447 | 446 | 450 | Motif | Nuclear localization signal |
Tgene | >CLU | chr9:139872144 | chr8:27455767 | ENST00000523500 | - | 6 | 8 | 443_447 | 446 | 450 | Motif | Nuclear localization signal |
- 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 |
Tgene | CLU | chr9:139872144 | chr8:27455767 | ENST00000316403 | - | 7 | 9 | 78_81 | 446 | 450 | Motif | Nuclear localization signal |
Tgene | CLU | chr9:139872144 | chr8:27455767 | ENST00000405140 | - | 7 | 9 | 78_81 | 446 | 450 | Motif | Nuclear localization signal |
Tgene | CLU | chr9:139872144 | chr8:27455767 | ENST00000523500 | - | 6 | 8 | 78_81 | 446 | 450 | Motif | Nuclear localization signal |
Tgene | CLU | chr9:139872144 | chr8:27455767 | ENST00000546343 | - | 7 | 9 | 443_447 | 457 | 461 | Motif | Nuclear localization signal |
Tgene | CLU | chr9:139872144 | chr8:27455767 | ENST00000546343 | - | 7 | 9 | 78_81 | 457 | 461 | Motif | Nuclear localization signal |
Tgene | CLU | chr9:139872144 | chr8:27455767 | ENST00000560366 | - | 7 | 9 | 443_447 | 498 | 502 | Motif | Nuclear localization signal |
Tgene | CLU | chr9:139872144 | chr8:27455767 | ENST00000560366 | - | 7 | 9 | 78_81 | 498 | 502 | Motif | Nuclear localization signal |
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FusionGeneSequence for PTGDS_CLU |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
>In-frame_PTGDS_ENST00000224167_chr9_139872144_+_CLU_ENST00000316403_chr8_27455767_-_41aa >In-frame_PTGDS_ENST00000224167_chr9_139872144_+_CLU_ENST00000405140_chr8_27455767_-_41aa >In-frame_PTGDS_ENST00000371625_chr9_139872144_+_CLU_ENST00000316403_chr8_27455767_-_41aa >In-frame_PTGDS_ENST00000371625_chr9_139872144_+_CLU_ENST00000405140_chr8_27455767_-_41aa |
* Fusion transcript sequences (only coding sequence (CDS) region). |
>In-frame_PTGDS_ENST00000224167_chr9_139872144_+_CLU_ENST00000316403_chr8_27455767_-_124nt ATGGCTACTCATCACACACTGTGGATGGGACTGGCCCTGCTGGGGGTGCTGGGCGACCTGCAGGCAGCACCGGAGGCCCAGGTCTCCGTG >In-frame_PTGDS_ENST00000224167_chr9_139872144_+_CLU_ENST00000405140_chr8_27455767_-_124nt ATGGCTACTCATCACACACTGTGGATGGGACTGGCCCTGCTGGGGGTGCTGGGCGACCTGCAGGCAGCACCGGAGGCCCAGGTCTCCGTG >In-frame_PTGDS_ENST00000371625_chr9_139872144_+_CLU_ENST00000316403_chr8_27455767_-_124nt ATGGCTACTCATCACACACTGTGGATGGGACTGGCCCTGCTGGGGGTGCTGGGCGACCTGCAGGCAGCACCGGAGGCCCAGGTCTCCGTG >In-frame_PTGDS_ENST00000371625_chr9_139872144_+_CLU_ENST00000405140_chr8_27455767_-_124nt ATGGCTACTCATCACACACTGTGGATGGGACTGGCCCTGCTGGGGGTGCTGGGCGACCTGCAGGCAGCACCGGAGGCCCAGGTCTCCGTG |
* Fusion transcript sequences (Full-length transcript). |
>In-frame_PTGDS_ENST00000224167_chr9_139872144_+_CLU_ENST00000316403_chr8_27455767_-_1523nt GCTCCTCCTGCACACCTCCCTCGCTCTCCCACACCACTGGCACCAGGCCCCGGACACCCGCTCTGCTGCAGGAGAATGGCTACTCATCAC ACACTGTGGATGGGACTGGCCCTGCTGGGGGTGCTGGGCGACCTGCAGGCAGCACCGGAGGCCCAGGTCTCCGTGCAGCCCAACTTCCAG CAGGACAAGGGAGGAGTGAGATGTGGATGTTGCTTTTGCACCTACGGGGGCATCTGAGTCCAGCTCCCCCCAAGATGAGCTGCAGCCCCC CAGAGAGAGCTCTGCACGTCACCAAGTAACCAGGCCCCAGCCTCCAGGCCCCCAACTCCGCCCAGCCTCTCCCCGCTCTGGATCCTGCAC TCTAACACTCGACTCTGCTGCTCATGGGAAGAACAGAATTGCTCCTGCATGCAACTAATTCAATAAAACTGTCTTGTGAGCTGATCGCTT GGAGGGTCCTCTTTTTATGTTGAGTTGCTGCTTCCCGGCATGCCTTCATTTTGCTATGGGGGGCAGGCAGGGGGGATGGAAAATAAGTAG AAACAAAAAAGCAGTGGCTAAGATGGTATAGGGACTGTCATACCAGTGAAGAATAAAAGGGTGAAGAATAAAAGGGATATGATGACAAGG TTGATCCACTTCAAGAATTGCTTGCTTTCAGGAAGAGAGATGTGTTTCAACAAGCCAACTAAAATATATTGCTGCAAATGGAAGCTTTTC TGTTCTATTATAAAACTGTCGATGTATTCTGACCAAGGTGCGACAATCTCCTAAAGGAATACACTGAAAGTTAAGGAGAAGAATCAGTAA GTGTAAGGTGTACTTGGTATTATAATGCATAATTGATGTTTTCGTTATGAAAACATTTGGTGCCCAGAAGTCCAAATTATCAGTTTTATT TGTAAGAGCTATTGCTTTTGCAGCGGTTTTATTTGTAAAAGCTGTTGATTTCGAGTTGTAAGAGCTCAGCATCCCAGGGGCATCTTCTTG ACTGTGGCATTTCCTGTCCACCGCCGGTTTATATGATCTTCATACCTTTCCCTGGACCACAGGCGTTTCTCGGCTTTTAGTCTGAACCAT AGCTGGGCTGCAGTACCCTACGCTGCCAGCAGGTGGCCATGACTACCCGTGGTACCAATCTCAGTCTTAAAGCTCAGGCTTTTCGTTCAT TAACATTCTCTGATAGAATTCTGGTCATCAGATGTACTGCAATGGAACAAAACTCATCTGGCTGCATCCCAGGTGTGTAGCAAAGTCCAC ATGTAAATTTATAGCTTAGAATATTCTTAAGTCACTGTCCCTTGTCTCTCTTTGAAGTTATAAACAACAAACTTAAAGCTTAGCTTATGT CCAAGGTAAGTATTTTAGCATGGCTGTCAAGGAAATTCAGAGTAAAGTCAGTGTGATTCACTTAATGATATACATTAATTAGAATTATGG >In-frame_PTGDS_ENST00000224167_chr9_139872144_+_CLU_ENST00000405140_chr8_27455767_-_632nt GCTCCTCCTGCACACCTCCCTCGCTCTCCCACACCACTGGCACCAGGCCCCGGACACCCGCTCTGCTGCAGGAGAATGGCTACTCATCAC ACACTGTGGATGGGACTGGCCCTGCTGGGGGTGCTGGGCGACCTGCAGGCAGCACCGGAGGCCCAGGTCTCCGTGCAGCCCAACTTCCAG CAGGACAAGGGAGGAGTGAGATGTGGATGTTGCTTTTGCACCTACGGGGGCATCTGAGTCCAGCTCCCCCCAAGATGAGCTGCAGCCCCC CAGAGAGAGCTCTGCACGTCACCAAGTAACCAGGCCCCAGCCTCCAGGCCCCCAACTCCGCCCAGCCTCTCCCCGCTCTGGATCCTGCAC TCTAACACTCGACTCTGCTGCTCATGGGAAGAACAGAATTGCTCCTGCATGCAACTAATTCAATAAAACTGTCTTGTGAGCTGATCGCTT GGAGGGTCCTCTTTTTATGTTGAGTTGCTGCTTCCCGGCATGCCTTCATTTTGCTATGGGGGGCAGGCAGGGGGGATGGAAAATAAGTAG AAACAAAAAAGCAGTGGCTAAGATGGTATAGGGACTGTCATACCAGTGAAGAATAAAAGGGTGAAGAATAAAAGGGATATGATGACAAGG >In-frame_PTGDS_ENST00000371625_chr9_139872144_+_CLU_ENST00000316403_chr8_27455767_-_1522nt CTCCTCCTGCACACCTCCCTCGCTCTCCCACACCACTGGCACCAGGCCCCGGACACCCGCTCTGCTGCAGGAGAATGGCTACTCATCACA CACTGTGGATGGGACTGGCCCTGCTGGGGGTGCTGGGCGACCTGCAGGCAGCACCGGAGGCCCAGGTCTCCGTGCAGCCCAACTTCCAGC AGGACAAGGGAGGAGTGAGATGTGGATGTTGCTTTTGCACCTACGGGGGCATCTGAGTCCAGCTCCCCCCAAGATGAGCTGCAGCCCCCC AGAGAGAGCTCTGCACGTCACCAAGTAACCAGGCCCCAGCCTCCAGGCCCCCAACTCCGCCCAGCCTCTCCCCGCTCTGGATCCTGCACT CTAACACTCGACTCTGCTGCTCATGGGAAGAACAGAATTGCTCCTGCATGCAACTAATTCAATAAAACTGTCTTGTGAGCTGATCGCTTG GAGGGTCCTCTTTTTATGTTGAGTTGCTGCTTCCCGGCATGCCTTCATTTTGCTATGGGGGGCAGGCAGGGGGGATGGAAAATAAGTAGA AACAAAAAAGCAGTGGCTAAGATGGTATAGGGACTGTCATACCAGTGAAGAATAAAAGGGTGAAGAATAAAAGGGATATGATGACAAGGT TGATCCACTTCAAGAATTGCTTGCTTTCAGGAAGAGAGATGTGTTTCAACAAGCCAACTAAAATATATTGCTGCAAATGGAAGCTTTTCT GTTCTATTATAAAACTGTCGATGTATTCTGACCAAGGTGCGACAATCTCCTAAAGGAATACACTGAAAGTTAAGGAGAAGAATCAGTAAG TGTAAGGTGTACTTGGTATTATAATGCATAATTGATGTTTTCGTTATGAAAACATTTGGTGCCCAGAAGTCCAAATTATCAGTTTTATTT GTAAGAGCTATTGCTTTTGCAGCGGTTTTATTTGTAAAAGCTGTTGATTTCGAGTTGTAAGAGCTCAGCATCCCAGGGGCATCTTCTTGA CTGTGGCATTTCCTGTCCACCGCCGGTTTATATGATCTTCATACCTTTCCCTGGACCACAGGCGTTTCTCGGCTTTTAGTCTGAACCATA GCTGGGCTGCAGTACCCTACGCTGCCAGCAGGTGGCCATGACTACCCGTGGTACCAATCTCAGTCTTAAAGCTCAGGCTTTTCGTTCATT AACATTCTCTGATAGAATTCTGGTCATCAGATGTACTGCAATGGAACAAAACTCATCTGGCTGCATCCCAGGTGTGTAGCAAAGTCCACA TGTAAATTTATAGCTTAGAATATTCTTAAGTCACTGTCCCTTGTCTCTCTTTGAAGTTATAAACAACAAACTTAAAGCTTAGCTTATGTC CAAGGTAAGTATTTTAGCATGGCTGTCAAGGAAATTCAGAGTAAAGTCAGTGTGATTCACTTAATGATATACATTAATTAGAATTATGGG >In-frame_PTGDS_ENST00000371625_chr9_139872144_+_CLU_ENST00000405140_chr8_27455767_-_631nt CTCCTCCTGCACACCTCCCTCGCTCTCCCACACCACTGGCACCAGGCCCCGGACACCCGCTCTGCTGCAGGAGAATGGCTACTCATCACA CACTGTGGATGGGACTGGCCCTGCTGGGGGTGCTGGGCGACCTGCAGGCAGCACCGGAGGCCCAGGTCTCCGTGCAGCCCAACTTCCAGC AGGACAAGGGAGGAGTGAGATGTGGATGTTGCTTTTGCACCTACGGGGGCATCTGAGTCCAGCTCCCCCCAAGATGAGCTGCAGCCCCCC AGAGAGAGCTCTGCACGTCACCAAGTAACCAGGCCCCAGCCTCCAGGCCCCCAACTCCGCCCAGCCTCTCCCCGCTCTGGATCCTGCACT CTAACACTCGACTCTGCTGCTCATGGGAAGAACAGAATTGCTCCTGCATGCAACTAATTCAATAAAACTGTCTTGTGAGCTGATCGCTTG GAGGGTCCTCTTTTTATGTTGAGTTGCTGCTTCCCGGCATGCCTTCATTTTGCTATGGGGGGCAGGCAGGGGGGATGGAAAATAAGTAGA AACAAAAAAGCAGTGGCTAAGATGGTATAGGGACTGTCATACCAGTGAAGAATAAAAGGGTGAAGAATAAAAGGGATATGATGACAAGGT |
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FusionGenePPI for PTGDS_CLU |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
PTGDS | EGFR, CACNA1A, SHBG, ATXN1, MLH1, PTGDS, CAPN1, BCAT2, RARRES3, ARRB2, PTGDR, HSP90AA1, KRTAP10-7, KRTAP10-3, AKT1, FBXW7, ORM1, CHN2 | CLU | CLU, TGFBR2, MMP25, XRCC6, C8B, C7, C9, LRP2, TGFBR1, SYVN1, H2AFX, COMMD1, NFKB1, NFKBIA, CUL1, BTRC, DISC1, TNIK, GRB2, RAD21, VHL, CHUK, TTR, BAX, CD209, XPO1, ACTN1, ZWINT, KATNA1, KNSTRN, SLC4A1, HBA1, CBY1, ELN, APP, LYZ, ATP7B, ATP7A, BCL2L1, CLUAP1, IL24, HSPD1, PRNP, PON1, FBXO6, PAXIP1, LIG4, MDC1, PDIA3, APOA1, POLR1C, BAG6, CYP2E1, MAPK9, RBBP8, KLF11, RPL23, KEAP1, TSC22D4, FOS, MDM2, CDK19, HSPA1L, NUCB2, TUBB6, TUFM, HSPA5, HSP90B1, HYOU1, UBC, EGFR, RPE, HLA-DPA1, HAX1, CCND3, DPPA4, IL20RB, SUMF2, GPR180, GINM1, SDF4, MMP3, RASSF7, TNF, RNASE13, IFNA5, PLK1, EPPIN, LTF, SEMG1, ADCYAP1R1, SRPK2, CANX, PDGFRA, ARMC6, TUBGCP5, FXR1, SETX, DOCK6, GPAM, ATG3, MAP1LC3A, MCM2, MMP9, VEGFA, SDK2, ATP2B2, PTPRS, TENM3, FAT4, FBXO27, CBWD3, KIAA0355, DHX57, ITGA8, EDEM2, MANEA, DDX31, ARHGAP36, EXTL2, TOR1A, MAN1A1, TNFSF9, PCYOX1L, PTPRF, GNB2, MAN1A2, CELSR1, NLGN2, TXNDC11, INTS5, PCYOX1, MTMR9, OCIAD1, LMAN2L, EIF3F |
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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 PTGDS_CLU |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | CLU | P10909 | DB01593 | Zinc | Clusterin | small molecule | approved|investigational |
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RelatedDiseases for PTGDS_CLU |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | PTGDS | C0005586 | Bipolar Disorder | 2 | PSYGENET |
Hgene | PTGDS | C0036341 | Schizophrenia | 1 | PSYGENET |
Tgene | CLU | C2609414 | Acute kidney injury | 5 | CTD_human |
Tgene | CLU | C0002395 | Alzheimer's Disease | 3 | CTD_human |
Tgene | CLU | C0022658 | Kidney Diseases | 3 | CTD_human |
Tgene | CLU | C0029408 | Degenerative polyarthritis | 2 | CTD_human |
Tgene | CLU | C0024141 | Lupus Erythematosus, Systemic | 1 | CTD_human |
Tgene | CLU | C0025202 | melanoma | 1 | CTD_human |
Tgene | CLU | C0027686 | Pathologic Neovascularization | 1 | CTD_human |
Tgene | CLU | C0033578 | Prostatic Neoplasms | 1 | CTD_human |
Tgene | CLU | C0036341 | Schizophrenia | 1 | PSYGENET |
Tgene | CLU | C0036572 | Seizures | 1 | CTD_human |
Tgene | CLU | C0041755 | Adverse reaction to drug | 1 | CTD_human |
Tgene | CLU | C0333641 | Atrophic | 1 | CTD_human |
Tgene | CLU | C1862939 | AMYOTROPHIC LATERAL SCLEROSIS 1 | 1 | CTD_human |
Tgene | CLU | C3495559 | Juvenile arthritis | 1 | CTD_human |
Tgene | CLU | C4277682 | Chemical and Drug Induced Liver Injury | 1 | CTD_human |