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Fusion gene ID: 13544 |
FusionGeneSummary for FKTN_TMEM38B |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: FKTN_TMEM38B | Fusion gene ID: 13544 | Hgene | Tgene | Gene symbol | FKTN | TMEM38B | Gene ID | 2218 | 55151 |
| Gene name | fukutin | transmembrane protein 38B | |
| Synonyms | CMD1X|FCMD|LGMD2M|MDDGA4|MDDGB4|MDDGC4 | C9orf87|D4Ertd89e|OI14|TRIC-B|TRICB|bA219P18.1 | |
| Cytomap | 9q31.2 | 9q31.2 | |
| Type of gene | protein-coding | protein-coding | |
| Description | fukutinFukuyama type congenital muscular dystrophy proteinpatient fukutin | trimeric intracellular cation channel type B | |
| Modification date | 20180523 | 20180519 | |
| UniProtAcc | O75072 | Q9NVV0 | |
| Ensembl transtripts involved in fusion gene | ENST00000602661, ENST00000223528, ENST00000540160, ENST00000448551, ENST00000357998, ENST00000490134, | ENST00000374692, ENST00000374688, | |
| Fusion gene scores | * DoF score | 3 X 3 X 3=27 | 3 X 2 X 3=18 |
| # samples | 3 | 3 | |
| ** MAII score | log2(3/27*10)=0.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(3/18*10)=0.736965594166206 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
| Context | PubMed: FKTN [Title/Abstract] AND TMEM38B [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 | LD | LUAD | TCGA-44-6146-01A | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| * 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 | ENST00000602661 | ENST00000374692 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| Frame-shift | ENST00000602661 | ENST00000374688 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| Frame-shift | ENST00000223528 | ENST00000374692 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| Frame-shift | ENST00000223528 | ENST00000374688 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| Frame-shift | ENST00000540160 | ENST00000374692 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| Frame-shift | ENST00000540160 | ENST00000374688 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| Frame-shift | ENST00000448551 | ENST00000374692 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| Frame-shift | ENST00000448551 | ENST00000374688 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| Frame-shift | ENST00000357998 | ENST00000374692 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| Frame-shift | ENST00000357998 | ENST00000374688 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| intron-3CDS | ENST00000490134 | ENST00000374692 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
| intron-3CDS | ENST00000490134 | ENST00000374688 | FKTN | chr9 | 108366773 | + | TMEM38B | chr9 | 108536146 | + |
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FusionProtFeatures for FKTN_TMEM38B |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| FKTN | TMEM38B |
| Glycosyltransferase involved in the biosynthesis of thephosphorylated O-mannosyl trisaccharide (N-acetylgalactosamine-beta-3-N-acetylglucosamine-beta-4-(phosphate-6-)mannose), acarbohydrate structure present in alpha-dystroglycan (DAG1).Required for normal location of POMGNT1 in Golgi membranes, andfor normal POMGNT1 activity (PubMed:17034757). May interact withand reinforce a large complex encompassing the outside and insideof muscle membranes. Could be involved in brain development.{ECO:0000269|PubMed:17034757, ECO:0000269|PubMed:25279699}. | Monovalent cation channel required for maintenance ofrapid intracellular calcium release. May act as a potassiumcounter-ion channel that functions in synchronization with calciumrelease from intracellular stores. {ECO:0000250|UniProtKB:Q9DAV9}. |
| 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 FKTN_TMEM38B |
| 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 FKTN_TMEM38B |
| 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 |
| FKTN | CNBP, HLA-DPA1, TMEM5, B4GAT1 | TMEM38B | ELAVL1, LRRTM2, TCTN2, TCTN3, VAPA, ABHD5, TMEM206, 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 FKTN_TMEM38B |
| 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 FKTN_TMEM38B |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | FKTN | C1969040 | MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2M | 4 | CTD_human;ORPHANET;UNIPROT |
| Hgene | FKTN | C2751052 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 | 3 | CTD_human;UNIPROT |
| Hgene | FKTN | C0410174 | Fukuyama Type Congenital Muscular Dystrophy | 2 | CTD_human;ORPHANET;UNIPROT |
| Hgene | FKTN | C0026850 | Muscular Dystrophy | 1 | CTD_human;HPO |
| Hgene | FKTN | C1969024 | CARDIOMYOPATHY, DILATED, 1X | 1 | CTD_human;UNIPROT |
| Tgene | TMEM38B | C4277682 | Chemical and Drug Induced Liver Injury | 1 | CTD_human |
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