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 | Fusion Gene Summary |
| Fusion Gene ORF analysis |
| Fusion Genomic Features |
| Fusion Protein Features |
| Fusion Gene Sequence |
| Fusion Gene PPI analysis |
| Related Drugs |
| Related Diseases |
Fusion gene:SLC11A2-ATP8B1 (FusionGDB2 ID:81624) |
Fusion Gene Summary for SLC11A2-ATP8B1 |
 Fusion gene summary |
| Fusion gene information | Fusion gene name: SLC11A2-ATP8B1 | Fusion gene ID: 81624 | Hgene | Tgene | Gene symbol | SLC11A2 | ATP8B1 | Gene ID | 4891 | 5205 |
| Gene name | solute carrier family 11 member 2 | ATPase phospholipid transporting 8B1 | |
| Synonyms | AHMIO1|DCT1|DMT1|NRAMP2 | ATPIC|BRIC|FIC1|ICP1|PFIC|PFIC1 | |
| Cytomap | 12q13.12 | 18q21.31 | |
| Type of gene | protein-coding | protein-coding | |
| Description | natural resistance-associated macrophage protein 2DMT-1NRAMP 2divalent cation transporter 1solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2solute carrier family 11 (proton-coupled divalent metal ion transporters), me | phospholipid-transporting ATPase ICATPase, aminophospholipid transporter, class I, type 8B, member 1ATPase, class I, type 8B, member 1E1-E2 ATPaseP4-ATPase flippase complex alpha subunit ATP8B1familial intrahepatic cholestasis type 1probable phospho | |
| Modification date | 20200315 | 20200313 | |
| UniProtAcc | . | O43520 | |
| Ensembl transtripts involved in fusion gene | ENST00000262051, ENST00000547198, ENST00000262052, ENST00000394904, ENST00000547688, ENST00000541174, ENST00000545993, ENST00000546743, ENST00000549193, | ENST00000536015, ENST00000283684, ENST00000589147, | |
| Fusion gene scores | * DoF score | 8 X 8 X 6=384 | 11 X 11 X 4=484 |
| # samples | 9 | 11 | |
| ** MAII score | log2(9/384*10)=-2.09310940439148 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(11/484*10)=-2.13750352374993 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
| Context | PubMed: SLC11A2 [Title/Abstract] AND ATP8B1 [Title/Abstract] AND fusion [Title/Abstract] | ||
| Most frequent breakpoint | SLC11A2(51420098)-ATP8B1(55365099), # samples:1 | ||
| Anticipated loss of major functional domain due to fusion event. | |||
| * 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 | SLC11A2 | GO:0006825 | copper ion transport | 12734107 |
| Hgene | SLC11A2 | GO:0006826 | iron ion transport | 12734107|17293870 |
| Hgene | SLC11A2 | GO:0006828 | manganese ion transport | 17293870 |
| Hgene | SLC11A2 | GO:0015692 | lead ion transport | 12127992 |
| Hgene | SLC11A2 | GO:0034755 | iron ion transmembrane transport | 17293870 |
| Hgene | SLC11A2 | GO:0070574 | cadmium ion transmembrane transport | 12662899|25326704 |
| Tgene | ATP8B1 | GO:0006855 | drug transmembrane transport | 20510206 |
| Tgene | ATP8B1 | GO:0045332 | phospholipid translocation | 20510206 |
| Fusion gene breakpoints across SLC11A2 (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
| Fusion gene breakpoints across ATP8B1 (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
| 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 | LUSC | TCGA-77-8007-01A | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
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Fusion Gene ORF analysis for SLC11A2-ATP8B1 |
| 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 | ENST00000262051 | ENST00000536015 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-3CDS | ENST00000262051 | ENST00000283684 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-5UTR | ENST00000262051 | ENST00000589147 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-3CDS | ENST00000547198 | ENST00000536015 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-3CDS | ENST00000547198 | ENST00000283684 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-5UTR | ENST00000547198 | ENST00000589147 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-3CDS | ENST00000262052 | ENST00000536015 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-3CDS | ENST00000262052 | ENST00000283684 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-5UTR | ENST00000262052 | ENST00000589147 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-3CDS | ENST00000394904 | ENST00000536015 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-3CDS | ENST00000394904 | ENST00000283684 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-5UTR | ENST00000394904 | ENST00000589147 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-3CDS | ENST00000547688 | ENST00000536015 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-3CDS | ENST00000547688 | ENST00000283684 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-5UTR | ENST00000547688 | ENST00000589147 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-3CDS | ENST00000541174 | ENST00000536015 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-3CDS | ENST00000541174 | ENST00000283684 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-5UTR | ENST00000541174 | ENST00000589147 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-3CDS | ENST00000545993 | ENST00000536015 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-3CDS | ENST00000545993 | ENST00000283684 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-5UTR | ENST00000545993 | ENST00000589147 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-3CDS | ENST00000546743 | ENST00000536015 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-3CDS | ENST00000546743 | ENST00000283684 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| 5UTR-5UTR | ENST00000546743 | ENST00000589147 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-3CDS | ENST00000549193 | ENST00000536015 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-3CDS | ENST00000549193 | ENST00000283684 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| intron-5UTR | ENST00000549193 | ENST00000589147 | SLC11A2 | chr12 | 51420098 | - | ATP8B1 | chr18 | 55365099 | - |
| ORFfinder result based on the fusion transcript sequence of in-frame fusion genes. |
| 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) |
| 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 |
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Fusion Genomic Features for SLC11A2-ATP8B1 |
| FusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints. |
| Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
| Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page. |
| Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page. |
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Fusion Protein Features for SLC11A2-ATP8B1 |
| Go to FGviewer for the breakpoints of :-: - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. |
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| Main function of each fusion partner protein. (from UniProt) |
| Hgene | Tgene |
| . | ATP8B1 |
| FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes. | FUNCTION: Catalytic component of a P4-ATPase flippase complex which catalyzes the hydrolysis of ATP coupled to the transport of phospholipids, in particular phosphatidylcholines (PC), from the outer to the inner leaflet of the plasma membrane (PubMed:25315773, PubMed:17948906). May participate in the establishment of the canalicular membrane integrity by ensuring asymmetric distribution of phospholipids in the canicular membrane (By similarity). Thus may have a role in the regulation of bile acids transport into the canaliculus, uptake of bile acids from intestinal contents into intestinal mucosa or both and protect hepatocytes from bile salts (By similarity). Involved in the microvillus formation in polarized epithelial cells; the function seems to be independent from its flippase activity (PubMed:20512993). Participates in correct apical membrane localization of CDC42, CFTR and SLC10A2 (PubMed:25239307, PubMed:27301931). Enables CDC42 clustering at the apical membrane during enterocyte polarization through the interaction between CDC42 polybasic region and negatively charged membrane lipids provided by ATP8B1 (By similarity). Together with TMEM30A is involved in uptake of the synthetic drug alkylphospholipid perifosine (PubMed:20510206). Required for the preservation of cochlear hair cells in the inner ear (By similarity). May act as cardiolipin transporter during inflammatory injury (By similarity). {ECO:0000250|UniProtKB:Q148W0, ECO:0000269|PubMed:17948906, ECO:0000269|PubMed:20510206, ECO:0000269|PubMed:20512993, ECO:0000269|PubMed:25239307, ECO:0000269|PubMed:27301931}. |
| 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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Fusion Gene Sequence for SLC11A2-ATP8B1 |
| For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
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Fusion Gene PPI Analysis for SLC11A2-ATP8B1 |
| 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 |
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Related Drugs for SLC11A2-ATP8B1 |
| Drugs targeting genes involved in this fusion gene. (DrugBank Version 5.1.8 2021-05-08) |
| Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Related Diseases for SLC11A2-ATP8B1 |
| Diseases associated with fusion partners. (DisGeNet 4.0) |
| Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
| Hgene | SLC11A2 | C3806153 | ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1 | 3 | GENOMICS_ENGLAND;UNIPROT |
| Hgene | SLC11A2 | C2673913 | Anemia, Hypochromic Microcytic, With Iron Overload | 2 | CTD_human;ORPHANET |
| Hgene | SLC11A2 | C0018995 | Hemochromatosis | 1 | CTD_human |
| Hgene | SLC11A2 | C0023903 | Liver neoplasms | 1 | CTD_human |
| Hgene | SLC11A2 | C0162316 | Iron deficiency anemia | 1 | CTD_human |
| Hgene | SLC11A2 | C0345904 | Malignant neoplasm of liver | 1 | CTD_human |
| Hgene | SLC11A2 | C0392514 | Hereditary hemochromatosis | 1 | CTD_human |
| Tgene | ATP8B1 | C4551898 | Cholestasis, progressive familial intrahepatic 1 | 7 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
| Tgene | ATP8B1 | C4551899 | Cholestasis, benign recurrent intrahepatic 1 | 5 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
| Tgene | ATP8B1 | C3549845 | CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1 | 4 | GENOMICS_ENGLAND;UNIPROT |
| Tgene | ATP8B1 | C0008372 | Intrahepatic Cholestasis | 1 | CTD_human |
| Tgene | ATP8B1 | C0268318 | Cholestasis of pregnancy | 1 | CTD_human;ORPHANET |
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