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Fusion gene ID: 29851 |
FusionGeneSummary for R3HDM2_PRDM9 |
Fusion gene summary |
Fusion gene information | Fusion gene name: R3HDM2_PRDM9 | Fusion gene ID: 29851 | Hgene | Tgene | Gene symbol | R3HDM2 | PRDM9 | Gene ID | 22864 | 56979 |
Gene name | R3H domain containing 2 | PR/SET domain 9 | |
Synonyms | CAG6|PR01365 | KMT8B|MEISETZ|MSBP3|PFM6|ZNF899 | |
Cytomap | 12q13.3 | 5p14.2 | |
Type of gene | protein-coding | protein-coding | |
Description | R3H domain-containing protein 2 | histone-lysine N-methyltransferase PRDM9PR domain 9PR domain containing 9PR domain zinc finger protein 9histone methyl transferaseminisatellite binding protein 3 (115kD) | |
Modification date | 20180519 | 20180523 | |
UniProtAcc | Q9Y2K5 | Q9NQV7 | |
Ensembl transtripts involved in fusion gene | ENST00000413953, ENST00000347140, ENST00000358907, ENST00000402412, ENST00000441731, ENST00000403821, ENST00000546843, | ENST00000296682, | |
Fusion gene scores | * DoF score | 29 X 12 X 9=3132 | 1 X 1 X 1=1 |
# samples | 28 | 1 | |
** MAII score | log2(28/3132*10)=-3.48358548034607 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(1/1*10)=3.32192809488736 | |
Context | PubMed: R3HDM2 [Title/Abstract] AND PRDM9 [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) |
Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | PRDM9 | GO:0006311 | meiotic gene conversion | 21750151 |
Fusion gene information from three resources (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 | SKCM | TCGA-EB-A44Q-06A | R3HDM2 | chr12 | 57824503 | - | PRDM9 | chr5 | 23493580 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure. * 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 | ENST00000413953 | ENST00000296682 | R3HDM2 | chr12 | 57824503 | - | PRDM9 | chr5 | 23493580 | + |
5UTR-intron | ENST00000347140 | ENST00000296682 | R3HDM2 | chr12 | 57824503 | - | PRDM9 | chr5 | 23493580 | + |
intron-intron | ENST00000358907 | ENST00000296682 | R3HDM2 | chr12 | 57824503 | - | PRDM9 | chr5 | 23493580 | + |
5UTR-intron | ENST00000402412 | ENST00000296682 | R3HDM2 | chr12 | 57824503 | - | PRDM9 | chr5 | 23493580 | + |
intron-intron | ENST00000441731 | ENST00000296682 | R3HDM2 | chr12 | 57824503 | - | PRDM9 | chr5 | 23493580 | + |
intron-intron | ENST00000403821 | ENST00000296682 | R3HDM2 | chr12 | 57824503 | - | PRDM9 | chr5 | 23493580 | + |
intron-intron | ENST00000546843 | ENST00000296682 | R3HDM2 | chr12 | 57824503 | - | PRDM9 | chr5 | 23493580 | + |
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FusionProtFeatures for R3HDM2_PRDM9 |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
R3HDM2 | PRDM9 |
Histone methyltransferase that specificallytrimethylates 'Lys-4' of histone H3 during meiotic prophase and isessential for proper meiotic progression. Does not have theability to mono- and dimethylate 'Lys-4' of histone H3. H3 'Lys-4'methylation represents a specific tag for epigenetictranscriptional activation. Plays a central role in thetranscriptional activation of genes during early meiotic prophase(By similarity). {ECO:0000250}. |
Retention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at . * 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 R3HDM2_PRDM9 |
For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. (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 R3HDM2_PRDM9 |
Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in . |
Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160) |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
R3HDM2 | ELAVL1, ATXN1, YWHAB, REL, SPRY1, RBPMS, FAM168A, KRTAP3-2, C1orf94, KRTAP10-8, KRTAP10-3, NOTCH2NL, STAT5A | PRDM9 |
- Retained PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
- Lost PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
- Retained PPIs, but lost function due to frame-shift fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for R3HDM2_PRDM9 |
Drugs targeting genes involved in this fusion gene. (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 R3HDM2_PRDM9 |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | R3HDM2 | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
Hgene | R3HDM2 | C3495559 | Juvenile arthritis | 1 | CTD_human |