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Fusion Protein:ATP6V1H-CHD7 |
Fusion Protein Summary |
 Fusion gene summary |
| Fusion partner gene information | Fusion gene name: ATP6V1H-CHD7 | FusionPDB ID: 8212 | FusionGDB2.0 ID: 8212 | Hgene | Tgene | Gene symbol | ATP6V1H | CHD7 | Gene ID | 51606 | 55636 |
| Gene name | ATPase H+ transporting V1 subunit H | chromodomain helicase DNA binding protein 7 | |
| Synonyms | CGI-11|MSTP042|NBP1|SFD|SFDalpha|SFDbeta|VMA13 | CRG|HH5|IS3|KAL5 | |
| Cytomap | 8q11.23 | 8q12.2 | |
| Type of gene | protein-coding | protein-coding | |
| Description | V-type proton ATPase subunit HATPase, H+ transporting, lysosomal 50/57kDa, V1 subunit HV-ATPase 50/57 kDa subunitsV-ATPase subunit Hnef-binding protein 1protein VMA13 homologvacuolar ATP synthase subunit Hvacuolar ATPase subunit Hvacuolar proton p | chromodomain-helicase-DNA-binding protein 7ATP-dependent helicase CHD7CHARGE associationchromodomain helicase DNA binding protein 7 isoform CRA_e | |
| Modification date | 20200313 | 20200328 | |
| UniProtAcc | Q9UI12 | Q9P2D1 | |
| Ensembl transtripts involved in fusion gene | ENST ids | ENST00000355221, ENST00000359530, ENST00000396774, ENST00000520188, ENST00000523899, | ENST00000529472, ENST00000423902, ENST00000524602, ENST00000525508, |
| Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 11 X 11 X 8=968 | 9 X 5 X 6=270 |
| # samples | 15 | 9 | |
| ** MAII score | log2(15/968*10)=-2.69004454677871 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(9/270*10)=-1.58496250072116 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context (manual curation of fusion genes in FusionPDB) | PubMed: ATP6V1H [Title/Abstract] AND CHD7 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | ATP6V1H(54754138)-CHD7(61693559), # samples:2 | ||
| Anticipated loss of major functional domain due to fusion event. | ATP6V1H-CHD7 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. ATP6V1H-CHD7 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. ATP6V1H-CHD7 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. ATP6V1H-CHD7 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. ATP6V1H-CHD7 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. ATP6V1H-CHD7 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF. ATP6V1H-CHD7 seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF. ATP6V1H-CHD7 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. | ||
| * 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 | ATP6V1H | GO:0006897 | endocytosis | 12032142 |
| Fusion gene breakpoints across ATP6V1H (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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| Fusion gene breakpoints across CHD7 (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
| Fusion gene information from FusionGDB2.0. |
| Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0) * 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. |
| Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
| ChimerDB4 | BRCA | TCGA-C8-A138-01A | ATP6V1H | chr8 | 54754138 | - | CHD7 | chr8 | 61693559 | + |
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Fusion ORF Analysis |
| Fusion information from ORFfinder translation from full-length transcript sequence from FusionPDB. |
| Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
| ENST00000396774 | ATP6V1H | chr8 | 54754138 | - | ENST00000423902 | CHD7 | chr8 | 61693559 | + | 8622 | 320 | 26 | 7648 | 2540 |
| ENST00000396774 | ATP6V1H | chr8 | 54754138 | - | ENST00000524602 | CHD7 | chr8 | 61693559 | + | 2043 | 320 | 26 | 1501 | 491 |
| ENST00000396774 | ATP6V1H | chr8 | 54754138 | - | ENST00000525508 | CHD7 | chr8 | 61693559 | + | 3432 | 320 | 26 | 2071 | 681 |
| DeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated. |
| Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
| ENST00000396774 | ENST00000423902 | ATP6V1H | chr8 | 54754138 | - | CHD7 | chr8 | 61693559 | + | 0.000786036 | 0.99921393 |
| ENST00000396774 | ENST00000524602 | ATP6V1H | chr8 | 54754138 | - | CHD7 | chr8 | 61693559 | + | 0.001089932 | 0.99891007 |
| ENST00000396774 | ENST00000525508 | ATP6V1H | chr8 | 54754138 | - | CHD7 | chr8 | 61693559 | + | 0.000552254 | 0.99944776 |
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Fusion Amino Acid Sequences |
| For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
| >FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >8212_8212_1_ATP6V1H-CHD7_ATP6V1H_chr8_54754138_ENST00000396774_CHD7_chr8_61693559_ENST00000423902_length(amino acids)=2540AA_BP=183 MFGLRLQTRSGDSCSFSSLPGACWCLAAWSSPVLRPPVARLLFFQASTRFVERHSRLRSLDDQNGYPRCCGCCCPHQYYCCQGCRSSCKQ SQLAILSSHSPSEPFLEKPVPDMTQVSGPNAQLVKSDDYLPSIEQQPQQKKKKKKNNHIVAEDPSKGFGKDDFPGGVDNQELNRNSLDGS QEEKKKKKRSKAKKDPKEPKEPKEKKEPKEPKTPKAPKIPKEPKEKKAKTATPKPKSSKKSSNKKPDSEASALKKKVNKGKTEGSENSDL DKTPPPSPPPEEDEDPGVQKRRSSRQVKRKRYTEDLEFKISDEEADDADAAGRDSPSNTSQSEQQESVDAEGPVVEKIMSSRSVKKQKES GEEVEIEEFYVKYKNFSYLHCQWASIEDLEKDKRIQQKIKRFKAKQGQNKFLSEIEDELFNPDYVEVDRIMDFARSTDDRGEPVTHYLVK WCSLPYEDSTWERRQDIDQAKIEEFEKLMSREPETERVERPPADDWKKSESSREYKNNNKLREYQLEGVNWLLFNWYNMRNCILADEMGL GKTIQSITFLYEIYLKGIHGPFLVIAPLSTIPNWEREFRTWTELNVVVYHGSQASRRTIQLYEMYFKDPQGRVIKGSYKFHAIITTFEMI LTDCPELRNIPWRCVVIDEAHRLKNRNCKLLEGLKMMDLEHKVLLTGTPLQNTVEELFSLLHFLEPSRFPSETTFMQEFGDLKTEEQVQK LQAILKPMMLRRLKEDVEKNLAPKEETIIEVELTNIQKKYYRAILEKNFTFLSKGGGQANVPNLLNTMMELRKCCNHPYLINGAEEKILE EFKETHNAESPDFQLQAMIQAAGKLVLIDKLLPKLKAGGHRVLIFSQMVRCLDILEDYLIQRRYPYERIDGRVRGNLRQAAIDRFSKPDS DRFVFLLCTRAGGLGINLTAADTCIIFDSDWNPQNDLQAQARCHRIGQSKSVKIYRLITRNSYEREMFDKASLKLGLDKAVLQSMSGREN ATNGVQQLSKKEIEDLLRKGAYGALMDEEDEGSKFCEEDIDQILLRRTHTITIESEGKGSTFAKASFVASGNRTDISLDDPNFWQKWAKK AELDIDALNGRNNLVIDTPRVRKQTRLYSAVKEDELMEFSDLESDSEEKPCAKPRRPQDKSQGYARSECFRVEKNLLVYGWGRWTDILSH GRYKRQLTEQDVETICRTILVYCLNHYKGDENIKSFIWDLITPTADGQTRALVNHSGLSAPVPRGRKGKKVKAQSTQPVVQDADWLASCN PDALFQEDSYKKHLKHHCNKVLLRVRMLYYLRQEVIGDQADKILEGADSSEADVWIPEPFHAEVPADWWDKEADKSLLIGVFKHGYEKYN SMRADPALCFLERVGMPDAKAIAAEQRGTDMLADGGDGGEFDREDEDPEYKPTRTPFKDEIDEFANSPSEDKEESMEIHATGKHSESNAE LGQLYWPNTSTLTTRLRRLITAYQRSYKRQQMRQEALMKTDRRRRRPREEVRALEAEREAIISEKRQKWTRREEADFYRVVSTFGVIFDP VKQQFDWNQFRAFARLDKKSDESLEKYFSCFVAMCRRVCRMPVKPDDEPPDLSSIIEPITEERASRTLYRIELLRKIREQVLHHPQLGER LKLCQPSLDLPEWWECGRHDRDLLVGAAKHGVSRTDYHILNDPELSFLDAHKNFAQNRGAGNTSSLNPLAVGFVQTPPVISSAHIQDERV LEQAEGKVEEPENPAAKEKCEGKEEEEETDGSGKESKQECEAEASSVKNELKGVEVGADTGSKSISEKGSEEDEEEKLEDDDKSEESSQP EAGAVSRGKNFDEESNASMSTARDETRDGFYMEDGDPSVAQLLHERTFAFSFWPKDRVMINRLDNICEAVLKGKWPVNRRQMFDFQGLIP GYTPTTVDSPLQKRSFAELSMVGQASISGSEDITTSPQLSKEDALNLSVPRQRRRRRRKIEIEAERAAKRRNLMEMVAQLRESQVVSENG QEKVVDLSKASREATSSTSNFSSLSSKFILPNVSTPVSDAFKTQMELLQAGLSRTPTRHLLNGSLVDGEPPMKRRRGRRKNVEGLDLLFM SHKRTSLSAEDAEVTKAFEEDIETPPTRNIPSPGQLDPDTRIPVINLEDGTRLVGEDAPKNKDLVEWLKLHPTYTVDMPSYVPKNADVLF SSFQKPKQKRHRCRNPNKLDINTLTGEERVPVVNKRNGKKMGGAMAPPMKDLPRWLEENPEFAVAPDWTDIVKQSGFVPESMFDRLLTGP VVRGEGASRRGRRPKSEIARAAAAAAAVASTSGINPLLVNSLFAGMDLTSLQNLQNLQSLQLAGLMGFPPGLATAATAGGDAKNPAAVLP LMLPGMAGLPNVFGLGGLLNNPLSAATGNTTTASSQGEPEDSTSKGEEKGNENEDENKDSEKSTDAVSAADSANGSVGAATAPAGLPSNP LAFNPFLLSTMAPGLFYPSMFLPPGLGGLTLPGFPALAGLQNAVGSSEEKAADKAEGGPFKDGETLEGSDAEESLDKTAESSLLEDEIAQ -------------------------------------------------------------- >8212_8212_2_ATP6V1H-CHD7_ATP6V1H_chr8_54754138_ENST00000396774_CHD7_chr8_61693559_ENST00000524602_length(amino acids)=491AA_BP=96 MFGLRLQTRSGDSCSFSSLPGACWCLAAWSSPVLRPPVARLLFFQASTRFVERHSRLRSLDDQNGYPRCCGCCCPHQYYCCQGCRSSCKQ SQLAILSSHSPSEPFLEKPVPDMTQKPKQKRHRCRNPNKLDINTLTGEERVPVVNKRNGKKMGGAMAPPMKDLPRWLEENPEFAVAPDWT DIVKQSGFVPESMFDRLLTGPVVRGEGASRRGRRPKSEIARAAAAAAAVASTSGINPLLVNSLFAGMDLTSLQNLQNLQSLQLAGLMGFP PGLATAATAGGDAKNPAAVLPLMLPGMAGLPNVFGLGGLLNNPLSAATGNTTTASSQGEPEDSTSKGEEKGNENEDENKDSEKSTDAVSA ADSANGSVGAATAPAGLPSNPLAFNPFLLSTMAPGLFYPSMFLPPGLGGLTLPGFPALAGLQNAVGSSEEKAADKAEGGPFKDGETLEGS -------------------------------------------------------------- >8212_8212_3_ATP6V1H-CHD7_ATP6V1H_chr8_54754138_ENST00000396774_CHD7_chr8_61693559_ENST00000525508_length(amino acids)=681AA_BP=183 MFGLRLQTRSGDSCSFSSLPGACWCLAAWSSPVLRPPVARLLFFQASTRFVERHSRLRSLDDQNGYPRCCGCCCPHQYYCCQGCRSSCKQ SQLAILSSHSPSEPFLEKPVPDMTQVSGPNAQLVKSDDYLPSIEQQPQQKKKKKKNNHIVAEDPSKGFGKDDFPGGVDNQELNRNSLDGS QEEKKKKKRSKAKKDPKEPKEPKEKKEPKEPKTPKAPKIPKEPKEKKAKTATPKPKSSKKSSNKKPDSEASALKKKVNKGKTEGSENSDL DKTPPPSPPPEEDEDPGVQKRRSSRQVKRKRYTEDLEFKISDEEADDADAAGRDSPSNTSQSEQQESVDAEGPVVEKIMSSRSVKKQKES GEEVEIEEFYVKYKNFSYLHCQWASIEDLEKDKRIQQKIKRFKAKQGQNKFLSEIEDELFNPDYVEVDRIMDFARSTDDRGEPVTHYLVK WCSLPYEDSTWERRQDIDQAKIEEFEKLMSREPETERVERPPADDWKKSESSREYKNNNKLREYQLEGVNWLLFNWYNMRNCILADEMGL GKTIQSITFLYEIYLKGIHGPFLVIAPLSTIPNWEREFRTWTELNVVVYHGSQASRRTIQLYEMYFKDPQGRVIKGSYKFHAIITTFEMI -------------------------------------------------------------- |
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Fusion Protein Functional Features |
| Four levels of functional features of fusion genes Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr8:54754138/chr8:61693559) - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. - How to search 1. Put your fusion gene symbol. 2. Press the tab key until there will be shown the breakpoint information filled. 4. Go down and press 'Search' tab twice. 4. Go down to have the hyperlink of the search result. 5. Click the hyperlink. 6. See the FGviewer result for your fusion gene. |
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| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| ATP6V1H | CHD7 |
| FUNCTION: Subunit of the peripheral V1 complex of vacuolar ATPase. Subunit H activates the ATPase activity of the enzyme and couples ATPase activity to proton flow. Vacuolar ATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells, thus providing most of the energy required for transport processes in the vacuolar system (By similarity). Involved in the endocytosis mediated by clathrin-coated pits, required for the formation of endosomes. {ECO:0000250}. | FUNCTION: Probable transcription regulator. Maybe involved in the in 45S precursor rRNA production. {ECO:0000269|PubMed:22646239}. |
| 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. |
| - 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 |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 2401_2431 | 555.0 | 2998.0 | Coiled coil | Ontology_term=ECO:0000255 | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 2401_2431 | 555.0 | 949.0 | Coiled coil | Ontology_term=ECO:0000255 | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 2401_2431 | 555.0 | 1139.0 | Coiled coil | Ontology_term=ECO:0000255 | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 1939_1945 | 555.0 | 2998.0 | Compositional bias | Note=Poly-Arg | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 2165_2258 | 555.0 | 2998.0 | Compositional bias | Note=Glu-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 2398_2405 | 555.0 | 2998.0 | Compositional bias | Note=Poly-Arg | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 2726_2736 | 555.0 | 2998.0 | Compositional bias | Note=Poly-Ala | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 597_718 | 555.0 | 2998.0 | Compositional bias | Note=Lys-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 1939_1945 | 555.0 | 949.0 | Compositional bias | Note=Poly-Arg | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 2165_2258 | 555.0 | 949.0 | Compositional bias | Note=Glu-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 2398_2405 | 555.0 | 949.0 | Compositional bias | Note=Poly-Arg | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 2726_2736 | 555.0 | 949.0 | Compositional bias | Note=Poly-Ala | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 597_718 | 555.0 | 949.0 | Compositional bias | Note=Lys-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 1939_1945 | 555.0 | 1139.0 | Compositional bias | Note=Poly-Arg | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 2165_2258 | 555.0 | 1139.0 | Compositional bias | Note=Glu-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 2398_2405 | 555.0 | 1139.0 | Compositional bias | Note=Poly-Arg | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 2726_2736 | 555.0 | 1139.0 | Compositional bias | Note=Poly-Ala | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 597_718 | 555.0 | 1139.0 | Compositional bias | Note=Lys-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 1294_1464 | 555.0 | 2998.0 | Domain | Helicase C-terminal | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 800_867 | 555.0 | 2998.0 | Domain | Chromo 1 | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 882_947 | 555.0 | 2998.0 | Domain | Chromo 2 | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 980_1154 | 555.0 | 2998.0 | Domain | Helicase ATP-binding | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 1294_1464 | 555.0 | 949.0 | Domain | Helicase C-terminal | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 800_867 | 555.0 | 949.0 | Domain | Chromo 1 | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 882_947 | 555.0 | 949.0 | Domain | Chromo 2 | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 980_1154 | 555.0 | 949.0 | Domain | Helicase ATP-binding | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 1294_1464 | 555.0 | 1139.0 | Domain | Helicase C-terminal | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 800_867 | 555.0 | 1139.0 | Domain | Chromo 1 | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 882_947 | 555.0 | 1139.0 | Domain | Chromo 2 | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 980_1154 | 555.0 | 1139.0 | Domain | Helicase ATP-binding | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 1105_1108 | 555.0 | 2998.0 | Motif | Note=DEAH box | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 1105_1108 | 555.0 | 949.0 | Motif | Note=DEAH box | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 1105_1108 | 555.0 | 1139.0 | Motif | Note=DEAH box | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 993_1000 | 555.0 | 2998.0 | Nucleotide binding | ATP | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 993_1000 | 555.0 | 949.0 | Nucleotide binding | ATP | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 993_1000 | 555.0 | 1139.0 | Nucleotide binding | ATP |
| - 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 |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 151_222 | 555.0 | 2998.0 | Compositional bias | Note=Gln-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000423902 | 1 | 38 | 383_568 | 555.0 | 2998.0 | Compositional bias | Note=Pro-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 151_222 | 555.0 | 949.0 | Compositional bias | Note=Gln-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000524602 | 0 | 5 | 383_568 | 555.0 | 949.0 | Compositional bias | Note=Pro-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 151_222 | 555.0 | 1139.0 | Compositional bias | Note=Gln-rich | |
| Tgene | CHD7 | chr8:54754138 | chr8:61693559 | ENST00000525508 | 0 | 12 | 383_568 | 555.0 | 1139.0 | Compositional bias | Note=Pro-rich |
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Fusion Protein-Protein Interaction |
| 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 from validated records (BIOGRID-3.4.160) |
| Gene | PPI interactors |
| Protein-protein interactors based on sequence similarity (STRING) |
| Gene | STRING network |
| ATP6V1H | |
| CHD7 |
| - Retained interactions in fusion protein (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
| - Lost interactions due to fusion (protein functional feature from UniProt). |
| Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs to ATP6V1H-CHD7 |
| Drugs used for this fusion-positive patient. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to ATP6V1H-CHD7 |
| Diseases that have this fusion gene. (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
| Hgene | Tgene | Disease | Source | PMID |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
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