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Fusion gene ID: 7368 |
FusionGeneSummary for CLEC16A_TXNDC11 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: CLEC16A_TXNDC11 | Fusion gene ID: 7368 | Hgene | Tgene | Gene symbol | CLEC16A | TXNDC11 | Gene ID | 23274 | 51061 |
| Gene name | C-type lectin domain containing 16A | thioredoxin domain containing 11 | |
| Synonyms | Gop-1|KIAA0350 | EFP1 | |
| Cytomap | 16p13.13 | 16p13.13 | |
| Type of gene | protein-coding | protein-coding | |
| Description | protein CLEC16AC-type lectin domain family 16 member A | thioredoxin domain-containing protein 11EF-hand binding protein 1 | |
| Modification date | 20180527 | 20180519 | |
| UniProtAcc | Q2KHT3 | Q6PKC3 | |
| Ensembl transtripts involved in fusion gene | ENST00000409790, ENST00000409552, ENST00000465491, ENST00000381822, | ENST00000283033, ENST00000356957, ENST00000570917, | |
| Fusion gene scores | * DoF score | 9 X 7 X 6=378 | 3 X 3 X 3=27 |
| # samples | 12 | 4 | |
| ** MAII score | log2(12/378*10)=-1.65535182861255 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(4/27*10)=0.567040592723894 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
| Context | PubMed: CLEC16A [Title/Abstract] AND TXNDC11 [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 |
| 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 | RV | GBM | TCGA-41-5651-01A | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| TCGA | LD | GBM | TCGA-19-4065-02A | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| * 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 | ENST00000409790 | ENST00000283033 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| Frame-shift | ENST00000409790 | ENST00000356957 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| 5CDS-5UTR | ENST00000409790 | ENST00000570917 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| Frame-shift | ENST00000409552 | ENST00000283033 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| Frame-shift | ENST00000409552 | ENST00000356957 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| 5CDS-5UTR | ENST00000409552 | ENST00000570917 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| intron-3CDS | ENST00000465491 | ENST00000283033 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| intron-3CDS | ENST00000465491 | ENST00000356957 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| intron-5UTR | ENST00000465491 | ENST00000570917 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| intron-3CDS | ENST00000381822 | ENST00000283033 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| intron-3CDS | ENST00000381822 | ENST00000356957 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
| intron-5UTR | ENST00000381822 | ENST00000570917 | CLEC16A | chr16 | 11076848 | + | TXNDC11 | chr16 | 11778101 | - |
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FusionProtFeatures for CLEC16A_TXNDC11 |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| CLEC16A | TXNDC11 |
| Regulator of mitophagy through the upstream regulationof the RNF41/NRDP1-PRKN pathway. Mitophagy is a selective form ofautophagy necessary for mitochondrial quality control. TheRNF41/NRDP1-PRKN pathway regulates autophagosome-lysosome fusionduring late mitophagy. May protect RNF41/NRDP1 from proteosomaldegradation, RNF41/NRDP1 which regulates proteosomal degradationof PRKN. Plays a key role in beta cells functions by regulatingmitophagy/autophagy and mitochondrial health.{ECO:0000269|PubMed:24949970}. | May act as a redox regulator involved in DUOX proteinsfolding. The interaction with DUOX1 and DUOX2 suggest that itbelongs to a multiprotein complex constituting the thyroidH(2)O(2) generating system. It is however not sufficient to assistDUOX1 and DUOX2 in H(2)O(2) generation. |
| 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 CLEC16A_TXNDC11 |
| 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 CLEC16A_TXNDC11 |
| 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 |
| CLEC16A | WRAP73, RNF41, TSSC1, RAB39B | TXNDC11 | KRT15, ATXN7, GFI1B, NOS3, KRT18, ACAA1, CDKN1A, ORC5, RPS19, STAT5A, HSP90B1, SOCS3, RPS6KA5, RACGAP1, FBXO6, ENO1, MOV10, NXF1, KLK11, SUSD4, CREBBP, TXLNA, RBL2, ZNF703, USO1, CCDC102A, RBL1, PCNT, HAUS4, FBLN7, CHST8, OLFM1, SCARA3, PTEN, SORT1, VPS26B, NEDD1, EDEM2, DCT, PSMC5, OS9, CLU, ANGPTL7, CCNA2, MXD3, TRIM25 |
| - 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 CLEC16A_TXNDC11 |
| 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 CLEC16A_TXNDC11 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | CLEC16A | C0011854 | Diabetes Mellitus, Insulin-Dependent | 2 | CTD_human |
| Hgene | CLEC16A | C0026769 | Multiple Sclerosis | 2 | CTD_human |
| Hgene | CLEC16A | C0162538 | Immunoglobulin A deficiency (disorder) | 2 | CTD_human |
| Hgene | CLEC16A | C0001403 | Addison Disease | 1 | CTD_human |
| Hgene | CLEC16A | C0023892 | Biliary cirrhosis | 1 | CTD_human |
| Hgene | CLEC16A | C0024141 | Lupus Erythematosus, Systemic | 1 | CTD_human |
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