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Fusion gene ID: 15647 |
FusionGeneSummary for GTF2IRD1_SHFM1 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: GTF2IRD1_SHFM1 | Fusion gene ID: 15647 | Hgene | Tgene | Gene symbol | GTF2IRD1 | SHFM1 | Gene ID | 9569 | 7979 |
| Gene name | GTF2I repeat domain containing 1 | SEM1, 26S proteasome complex subunit | |
| Synonyms | BEN|CREAM1|GTF3|MUSTRD1|RBAP2|WBS|WBSCR11|WBSCR12|hMusTRD1alpha1 | C7orf76|DSS1|ECD|SHFD1|SHFM1|SHSF1|Shfdg1 | |
| Cytomap | 7q11.23 | 7q21.3 | |
| Type of gene | protein-coding | protein-coding | |
| Description | general transcription factor II-I repeat domain-containing protein 1USE B1-binding proteinWilliams-Beuren syndrome chromosome region 11binding factor for early enhancergeneral transcription factor 3general transcription factor IIImuscle TFII-I repea | 26S proteasome complex subunit SEM126S proteasome complex subunit DSS1deleted in split hand/split foot protein 1deleted in split-hand/split-foot 1split hand/foot deleted protein 1split hand/foot malformation (ectrodactyly) type 1split hand/foot malf | |
| Modification date | 20180522 | 20180523 | |
| UniProtAcc | Q9UHL9 | ||
| Ensembl transtripts involved in fusion gene | ENST00000265755, ENST00000455841, ENST00000424337, ENST00000476977, ENST00000489094, | ENST00000417009, ENST00000444799, ENST00000413065, ENST00000248566, ENST00000493858, | |
| Fusion gene scores | * DoF score | 9 X 5 X 8=360 | 2 X 2 X 2=8 |
| # samples | 10 | 2 | |
| ** MAII score | log2(10/360*10)=-1.84799690655495 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(2/8*10)=1.32192809488736 | |
| Context | PubMed: GTF2IRD1 [Title/Abstract] AND SHFM1 [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 | HNSC | TCGA-MT-A51X-01A | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| * 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 |
| 5UTR-3CDS | ENST00000265755 | ENST00000417009 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000265755 | ENST00000444799 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000265755 | ENST00000413065 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000265755 | ENST00000248566 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000265755 | ENST00000493858 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-3CDS | ENST00000455841 | ENST00000417009 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000455841 | ENST00000444799 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000455841 | ENST00000413065 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000455841 | ENST00000248566 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000455841 | ENST00000493858 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-3CDS | ENST00000424337 | ENST00000417009 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000424337 | ENST00000444799 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000424337 | ENST00000413065 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000424337 | ENST00000248566 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| 5UTR-intron | ENST00000424337 | ENST00000493858 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| intron-3CDS | ENST00000476977 | ENST00000417009 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| intron-intron | ENST00000476977 | ENST00000444799 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| intron-intron | ENST00000476977 | ENST00000413065 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| intron-intron | ENST00000476977 | ENST00000248566 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| intron-intron | ENST00000476977 | ENST00000493858 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| intron-3CDS | ENST00000489094 | ENST00000417009 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| intron-intron | ENST00000489094 | ENST00000444799 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| intron-intron | ENST00000489094 | ENST00000413065 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| intron-intron | ENST00000489094 | ENST00000248566 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
| intron-intron | ENST00000489094 | ENST00000493858 | GTF2IRD1 | chr7 | 73868506 | + | SHFM1 | chr7 | 96251955 | - |
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FusionProtFeatures for GTF2IRD1_SHFM1 |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| GTF2IRD1 | SHFM1 |
| May be a transcription regulator involved in cell-cycleprogression and skeletal muscle differentiation. May repress GTF2Itranscriptional functions, by preventing its nuclear residency, orby inhibiting its transcriptional activation. May contribute toslow-twitch fiber type specificity during myogenesis and inregenerating muscles. Binds troponin I slow-muscle fiber enhancer(USE B1). Binds specifically and with high affinity to the EFGsequences derived from the early enhancer of HOXC8 (Bysimilarity). {ECO:0000250, ECO:0000269|PubMed:11438732}. | Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}. |
| 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 GTF2IRD1_SHFM1 |
| 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 GTF2IRD1_SHFM1 |
| 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 |
| GTF2IRD1 | HDAC3, PIAS2, SMAD2, USF1, UBC, EXOSC4, BRCA1, MAGEA10, GTF2IRD2B, FBXW11, HNRNPD, SORT1, XRCC1, SYNCRIP, TOR1AIP1, SGTB, BAG6, WASF3, ZNF23, LRRIQ1, PPP2R2D, NOLC1, KIFAP3, AKNAD1, TRIM25, CBX5, CBX1, CBX3, SP1, ALMS1, ATF7IP, ATP2C1, HTRA4, INTS12, KPNA1, KPNA3, KPNA4, MBD3L1, PKP2, SPTLC1, TMEM55A, USP20, VIMP, DCAF6, KPNA2, PIAS1, ZC4H2, ZMYM5, PKP1, ZMYM2, ZMYM3 | SHFM1 | PCID2, BRCA2, NUDT21, MAP1LC3B, PSMD1, PSMD2, PSMD3, PSMD4, PSMD7, PSMD8, PSMD10, PSMD11, PSMD12, PSMD13, PSMD14, PSMC1, PSMC2, PSMC3, PSMC5, PSMC6, POLR2B, INTS2, INTS4, INTS5, INTS6, INTS7, INTS8, INTS9, INTS10, CPSF3L, LENG8, SAC3D1, RAD23A, PSMD6, PSMA7, PSMA6, PSMA2, PSMB1, PSMB4, BRCA1, PSMC4, BAG3, PIAS1, TRIM33, HSPA8, EIF3A, EIF3C, EEF1A1, EEF1A2, EEF1G, EEF2, DDX42, MDN1, RPF2, TAF2, YY1, TOP1, SIN3A, SND1, HNRNPU, RBM15B, RBM33, ATXN2, PRPF4B, WDR63, NARF, FEN1, CCDC39, CKAP5, DNAH6, TLN2, TXNRD1, UBE3A, UBE3C, RNF181, HUWE1, UBR4, PSMD9, PAAF1, POMP, PSMG1, PSMG2, PSMG3, PSME1, PSME2, PSME3, PSME4, PSMF1, ADRM1, KIAA0368, USP14, UCHL5, TXNL1, ZFAND2B, UBLCP1, USP15, USP38, USP7, RAD23B, UBQLN1, UBQLN2, UBQLN4, UBA7, UBE2G2, CUL1, CUL2, CUL4B, FBXO7, HECTD1, MARCH6, RNF126, LTN1, RNF219, STUB1, UBE3B, UBR1, UBR5, UBR7, NUB1, SUMO2, UBE2I, NEDD8, UBC, BAG1, BAG2, DDX39B, PRRC2A, PRRC2C, BAG6, UBL4A, VCP, UFD1L, NSFL1C, UBFD1, KRAS, RPA1, RAD51 |
| - 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 GTF2IRD1_SHFM1 |
| 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 GTF2IRD1_SHFM1 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | GTF2IRD1 | C0175702 | Williams Syndrome | 1 | CTD_human;ORPHANET |
| Hgene | GTF2IRD1 | C0376634 | Craniofacial Abnormalities | 1 | CTD_human |
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