|
||||||
|
 | |
| |
| |
| |
| |
|
Fusion gene ID: 40795 |
FusionGeneSummary for UNC13C_NMNAT2 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: UNC13C_NMNAT2 | Fusion gene ID: 40795 | Hgene | Tgene | Gene symbol | UNC13C | NMNAT2 | Gene ID | 440279 | 23057 |
| Gene name | unc-13 homolog C | nicotinamide nucleotide adenylyltransferase 2 | |
| Synonyms | - | C1orf15|PNAT2 | |
| Cytomap | 15q21.3 | 1q25.3 | |
| Type of gene | protein-coding | protein-coding | |
| Description | protein unc-13 homolog CMunc13-3unc-13-like 3 | nicotinamide/nicotinic acid mononucleotide adenylyltransferase 2NMN adenylyltransferase 2NMN/NaMN adenylyltransferase 2NaMN adenylyltransferase 2nicotinamide mononucleotide adenylyltransferase 2nicotinate-nucleotide adenylyltransferase 2pyridine nuc | |
| Modification date | 20180523 | 20180523 | |
| UniProtAcc | Q8NB66 | Q9BZQ4 | |
| Ensembl transtripts involved in fusion gene | ENST00000260323, ENST00000537900, ENST00000545554, ENST00000539562, | ENST00000294868, ENST00000287713, ENST00000473046, | |
| Fusion gene scores | * DoF score | 2 X 2 X 1=4 | 7 X 6 X 5=210 |
| # samples | 3 | 7 | |
| ** MAII score | log2(3/4*10)=2.90689059560852 | log2(7/210*10)=-1.58496250072116 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: UNC13C [Title/Abstract] AND NMNAT2 [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 |
| ChiTaRS3.1 | AK126960 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| * 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-3UTR | ENST00000260323 | ENST00000294868 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-3UTR | ENST00000260323 | ENST00000287713 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-intron | ENST00000260323 | ENST00000473046 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-3UTR | ENST00000537900 | ENST00000294868 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-3UTR | ENST00000537900 | ENST00000287713 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-intron | ENST00000537900 | ENST00000473046 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-3UTR | ENST00000545554 | ENST00000294868 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-3UTR | ENST00000545554 | ENST00000287713 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-intron | ENST00000545554 | ENST00000473046 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-3UTR | ENST00000539562 | ENST00000294868 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-3UTR | ENST00000539562 | ENST00000287713 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
| intron-intron | ENST00000539562 | ENST00000473046 | UNC13C | chr15 | 54388134 | + | NMNAT2 | chr1 | 183218069 | - |
Top |
FusionProtFeatures for UNC13C_NMNAT2 |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| UNC13C | NMNAT2 |
| May play a role in vesicle maturation during exocytosisas a target of the diacylglycerol second messenger pathway. May beinvolved in the regulation of synaptic transmission at parallelfiber - Purkinje cell synapses (By similarity). {ECO:0000250}. | Nicotinamide/nicotinate-nucleotide adenylyltransferasethat acts as an axon maintenance factor (By similarity). Catalyzesthe formation of NAD(+) from nicotinamide mononucleotide (NMN) andATP (PubMed:16118205, PubMed:17402747). Can also use thedeamidated form; nicotinic acid mononucleotide (NaMN) as substratebut with a lower efficiency (PubMed:16118205, PubMed:17402747).Cannot use triazofurin monophosphate (TrMP) as substrate(PubMed:16118205, PubMed:17402747). Also catalyzes the reversereaction, i.e. the pyrophosphorolytic cleavage of NAD(+)(PubMed:16118205, PubMed:17402747). For the pyrophosphorolyticactivity prefers NAD(+), NADH and NaAD as substrates and degradesnicotinic acid adenine dinucleotide phosphate (NHD) lesseffectively (PubMed:16118205, PubMed:17402747). Fails to cleavephosphorylated dinucleotides NADP(+), NADPH and NaADP(+)(PubMed:16118205, PubMed:17402747). Axon survival factor requiredfor the maintenance of healthy axons: acts by delaying Wallerianaxon degeneration, an evolutionarily conserved process that drivesthe loss of damaged axons (By similarity).{ECO:0000250|UniProtKB:Q8BNJ3, ECO:0000269|PubMed:16118205,ECO:0000269|PubMed:17402747}. |
| 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 |
Top |
FusionGeneSequence for UNC13C_NMNAT2 |
| 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). |
Top |
FusionGenePPI for UNC13C_NMNAT2 |
| 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 |
| - 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 |
Top |
RelatedDrugs for UNC13C_NMNAT2 |
| 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 |
Top |
RelatedDiseases for UNC13C_NMNAT2 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Copyright 2018-Present -The University of Texas Health Science Center at Houston (UTHealth)
|