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Fusion gene ID: 31889 |
FusionGeneSummary for RPL32_WNT7A |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: RPL32_WNT7A | Fusion gene ID: 31889 | Hgene | Tgene | Gene symbol | RPL32 | WNT7A | Gene ID | 6161 | 7476 |
| Gene name | ribosomal protein L32 | Wnt family member 7A | |
| Synonyms | L32|PP9932 | - | |
| Cytomap | 3p25.2 | 3p25.1 | |
| Type of gene | protein-coding | protein-coding | |
| Description | 60S ribosomal protein L32large ribosomal subunit protein eL32 | protein Wnt-7aproto-oncogene Wnt7a proteinwingless-type MMTV integration site family, member 7A | |
| Modification date | 20180523 | 20180523 | |
| UniProtAcc | P62910 | O00755 | |
| Ensembl transtripts involved in fusion gene | ENST00000429711, ENST00000396957, ENST00000273223, ENST00000435983, ENST00000396953, | ENST00000285018, ENST00000497808, | |
| Fusion gene scores | * DoF score | 5 X 5 X 3=75 | 6 X 5 X 5=150 |
| # samples | 5 | 6 | |
| ** MAII score | log2(5/75*10)=-0.584962500721156 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(6/150*10)=-1.32192809488736 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: RPL32 [Title/Abstract] AND WNT7A [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 |
| Hgene | RPL32 | GO:0002181 | cytoplasmic translation | 25957688 |
| Tgene | WNT7A | GO:0001502 | cartilage condensation | 17202865 |
| Tgene | WNT7A | GO:0002062 | chondrocyte differentiation | 17202865 |
| Tgene | WNT7A | GO:0021846 | cell proliferation in forebrain | 12843296 |
| Tgene | WNT7A | GO:0032270 | positive regulation of cellular protein metabolic process | 16805831 |
| Tgene | WNT7A | GO:0035659 | Wnt signaling pathway involved in wound healing, spreading of epidermal cells | 15802269 |
| Tgene | WNT7A | GO:0045893 | positive regulation of transcription, DNA-templated | 15802269 |
| Tgene | WNT7A | GO:0045944 | positive regulation of transcription by RNA polymerase II | 12857724 |
| Tgene | WNT7A | GO:0048864 | stem cell development | 12843296 |
| Tgene | WNT7A | GO:0050768 | negative regulation of neurogenesis | 12843296 |
| Tgene | WNT7A | GO:0051965 | positive regulation of synapse assembly | 18986540 |
| Tgene | WNT7A | GO:0060054 | positive regulation of epithelial cell proliferation involved in wound healing | 15802269 |
| Tgene | WNT7A | GO:0060070 | canonical Wnt signaling pathway | 12857724|15802269|18986540|28733458 |
| Tgene | WNT7A | GO:0060997 | dendritic spine morphogenesis | 21670302 |
| Tgene | WNT7A | GO:0090263 | positive regulation of canonical Wnt signaling pathway | 16805831 |
| Tgene | WNT7A | GO:1904891 | positive regulation of excitatory synapse assembly | 21670302 |
| Tgene | WNT7A | GO:2000463 | positive regulation of excitatory postsynaptic potential | 21670302 |
| 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 | OV | TCGA-10-0934-01A | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
| * 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 |
| Frame-shift | ENST00000429711 | ENST00000285018 | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
| 5CDS-intron | ENST00000429711 | ENST00000497808 | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
| Frame-shift | ENST00000396957 | ENST00000285018 | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
| 5CDS-intron | ENST00000396957 | ENST00000497808 | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
| Frame-shift | ENST00000273223 | ENST00000285018 | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
| 5CDS-intron | ENST00000273223 | ENST00000497808 | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
| Frame-shift | ENST00000435983 | ENST00000285018 | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
| 5CDS-intron | ENST00000435983 | ENST00000497808 | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
| Frame-shift | ENST00000396953 | ENST00000285018 | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
| 5CDS-intron | ENST00000396953 | ENST00000497808 | RPL32 | chr3 | 12880848 | - | WNT7A | chr3 | 13896300 | - |
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FusionProtFeatures for RPL32_WNT7A |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| RPL32 | WNT7A |
| Ligand for members of the frizzled family of seventransmembrane receptors. Functions in the canonical Wnt/beta-catenin signaling pathway (By similarity). Plays an important rolein embryonic development, including dorsal versus ventralpatterning during limb development, skeleton development andurogenital tract development (PubMed:16826533). Required fornormal, sexually dimorphic development of the Mullerian ducts, andfor normal fertility in both sexes. Required for normal neuralstem cell proliferation in the hippocampus dentate gyrus. Requiredfor normal progress through the cell cycle in neural progenitorcells, for self-renewal of neural stem cells, and for normalneuronal differentiation and maturation. Promotes formation ofsynapses via its interaction with FZD5 (By similarity).{ECO:0000250|UniProtKB:P24383, ECO:0000269|PubMed:16826533}. |
| 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 RPL32_WNT7A |
| 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 RPL32_WNT7A |
| 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 |
| RPL32 | PSTPIP1, HDGF, CDK2, CUL1, COPS5, CAND1, RPL10A, RPL12, RPL14, RPL15, RPL18, RPL19, RPL21, RPL5, RPL7, RPL8, RPL9, RPS23, RPS26, RPS2, RPS3, RPS4X, RPS6, RPL23A, RPL7A, RPS8, RPL4, RPSA, RPS20, RPL17, RPS15A, RPS16, RPL23, RPS3A, RPL18A, RPL3, RPL29, ILF3, TUFM, HSP90AB1, CDH2, RPLP0P6, NACA2, MTHFD1, HSP90AA1, CALU, NENF, UBL4A, PAN2, FBXO6, TARDBP, BRCA1, RNF2, ABCE1, DHX8, THAP7, ZC3H3, RPL27A, RPL11, RPL13A, RPL24, RPL27, RPL34, RPL6, RPLP0, RPS11, RPS15, RPS9, SLC1A2, RPL35A, RPL37A, RPL39, RPS13, UBA52, HIST1H3E, HNRNPU, KIF11, NPM1, RPL10, NOP56, MCM2, DUSP11, DUSP5, MAK16, CNBP, ZNF512, RPL30, RBM34, KIAA0020, MAGEB10, RRP8, RPS14, RPL28, WDR46, RBM4, MECP2, ZC3HAV1, RRS1, ZBTB48, GPATCH4, PRPF3, PRPF4, ALYREF, FAU, LSM4, LSM8, RPL26L1, SART3, PPIH, CYLD, COX15, PDHA1, FOXA1, TRIM25 | WNT7A | WNT7B, WNT5A, TUBB1, MAPK9, WLS, PPP2CA, NPTX1, FBLN1, CRELD2, LOXL2, TUBA4A, RSPRY1, TUBB8, PIK3AP1, SDF2L1, PPP2R2D, TUBB3, HSPA5, FUT11, PASK, FSTL1, COL6A1, CALR, TUBA1A, CANX, LDLR |
| - 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 RPL32_WNT7A |
| 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 RPL32_WNT7A |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Tgene | WNT7A | C1848651 | Al Awadi syndrome | 4 | CTD_human;ORPHANET;UNIPROT |
| Tgene | WNT7A | C0042065 | Genitourinary Neoplasms | 1 | CTD_human |
| Tgene | WNT7A | C0919267 | ovarian neoplasm | 1 | CTD_human |
| Tgene | WNT7A | C1720887 | Female Urogenital Diseases | 1 | CTD_human |
| Tgene | WNT7A | C1856728 | Fuhrmann syndrome | 1 | CTD_human;ORPHANET;UNIPROT |
| Tgene | WNT7A | C1862939 | AMYOTROPHIC LATERAL SCLEROSIS 1 | 1 | CTD_human |
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