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Fusion gene ID: 3418 |
FusionGeneSummary for ATP5J_HCN1 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: ATP5J_HCN1 | Fusion gene ID: 3418 | Hgene | Tgene | Gene symbol | ATP5J | HCN1 | Gene ID | 348980 |
| Gene name | hyperpolarization activated cyclic nucleotide gated potassium channel 1 | ||
| Synonyms | BCNG-1|BCNG1|EIEE24|HAC-2 | ||
| Cytomap | 5p12 | ||
| Type of gene | protein-coding | ||
| Description | potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1brain cyclic nucleotide-gated channel 1 | ||
| Modification date | 20180522 | ||
| UniProtAcc | P18859 | O60741 | |
| Ensembl transtripts involved in fusion gene | ENST00000400099, ENST00000400094, ENST00000284971, ENST00000457143, ENST00000400090, ENST00000400087, ENST00000400093, | ENST00000303230, | |
| Fusion gene scores | * DoF score | 3 X 3 X 2=18 | 5 X 4 X 5=100 |
| # samples | 3 | 5 | |
| ** MAII score | log2(3/18*10)=0.736965594166206 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(5/100*10)=-1 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: ATP5J [Title/Abstract] AND HCN1 [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 |
| Tgene | HCN1 | GO:0051289 | protein homotetramerization | 28086084 |
| Tgene | HCN1 | GO:0071320 | cellular response to cAMP | 22748890 |
| 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 | KIRP | TCGA-B9-A5W9-01A | ATP5J | chr21 | 27107164 | - | HCN1 | chr5 | 45462109 | - |
| * 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-3CDS | ENST00000400099 | ENST00000303230 | ATP5J | chr21 | 27107164 | - | HCN1 | chr5 | 45462109 | - |
| 5UTR-3CDS | ENST00000400094 | ENST00000303230 | ATP5J | chr21 | 27107164 | - | HCN1 | chr5 | 45462109 | - |
| 5UTR-3CDS | ENST00000284971 | ENST00000303230 | ATP5J | chr21 | 27107164 | - | HCN1 | chr5 | 45462109 | - |
| intron-3CDS | ENST00000457143 | ENST00000303230 | ATP5J | chr21 | 27107164 | - | HCN1 | chr5 | 45462109 | - |
| intron-3CDS | ENST00000400090 | ENST00000303230 | ATP5J | chr21 | 27107164 | - | HCN1 | chr5 | 45462109 | - |
| intron-3CDS | ENST00000400087 | ENST00000303230 | ATP5J | chr21 | 27107164 | - | HCN1 | chr5 | 45462109 | - |
| intron-3CDS | ENST00000400093 | ENST00000303230 | ATP5J | chr21 | 27107164 | - | HCN1 | chr5 | 45462109 | - |
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FusionProtFeatures for ATP5J_HCN1 |
| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| ATP5J | HCN1 |
| Mitochondrial membrane ATP synthase (F(1)F(0) ATPsynthase or Complex V) produces ATP from ADP in the presence of aproton gradient across the membrane which is generated by electrontransport complexes of the respiratory chain. F-type ATPasesconsist of two structural domains, F(1) - containing theextramembraneous catalytic core and F(0) - containing the membraneproton channel, linked together by a central stalk and aperipheral stalk. During catalysis, ATP synthesis in the catalyticdomain of F(1) is coupled via a rotary mechanism of the centralstalk subunits to proton translocation. Part of the complex F(0)domain and the peripheric stalk, which acts as a stator to holdthe catalytic alpha(3)beta(3) subcomplex and subunit a/ATP6 staticrelative to the rotary elements. Also involved in the restorationof oligomycin-sensitive ATPase activity to depleted F1-F0complexes. | Hyperpolarization-activated ion channel exhibiting weakselectivity for potassium over sodium ions (PubMed:28086084).Contributes to the native pacemaker currents in heart (If) and inneurons (Ih). May mediate responses to sour stimuli.{ECO:0000269|PubMed:15351778, ECO:0000269|PubMed:28086084}. |
| 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 ATP5J_HCN1 |
| 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 ATP5J_HCN1 |
| 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 |
| ATP5J | BANF1, RPS6KA3, MAPK6, ATP5J2, ATP5O, UQCRC2, COA6, PARK7, ENO1, BLK, ATP5I, ACO2, ALDOA, ATP2B4, ATP5D, ATP5E, ENO3, FKBP7, FABP5, GSTO1, PRDX3, UQCRFS1, NDUFA13, GBA, RALA, TFEB, CDC16, ITGB3BP, GOLT1B, FAM134A, ATP5A1, NDUFA4, NDUFS3, PTPMT1, COQ9, C15orf48, CISD3, CHCHD2, COQ6, OCIAD1, OPA3, ACN9, ATP5B, ATP5F1 | HCN1 | HCN2, HCN3, HCN4, HCN1, NEDD4L |
| - 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 ATP5J_HCN1 |
| 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 ATP5J_HCN1 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Tgene | HCN1 | C0011581 | Depressive disorder | 2 | PSYGENET |
| Tgene | HCN1 | C0004134 | Ataxia | 1 | CTD_human |
| Tgene | HCN1 | C0011570 | Mental Depression | 1 | PSYGENET |
| Tgene | HCN1 | C0014544 | Epilepsy | 1 | CTD_human |
| Tgene | HCN1 | C0036572 | Seizures | 1 | CTD_human |
| Tgene | HCN1 | C3463992 | EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1 | 1 | CTD_human |
| Tgene | HCN1 | C4014531 | EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24 | 1 | UNIPROT |
Copyright 2018-Present -The University of Texas Health Science Center at Houston (UTHealth)
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