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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:ABCC2-CTNNA3 (FusionGDB2 ID:HG1244TG29119) |
Fusion Gene Summary for ABCC2-CTNNA3 |
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Fusion gene information | Fusion gene name: ABCC2-CTNNA3 | Fusion gene ID: hg1244tg29119 | Hgene | Tgene | Gene symbol | ABCC2 | CTNNA3 | Gene ID | 1244 | 29119 |
Gene name | ATP binding cassette subfamily C member 2 | catenin alpha 3 | |
Synonyms | ABC30|CMOAT|DJS|MRP2|cMRP | ARVD13|VR22 | |
Cytomap | ('ABCC2')('CTNNA3') 10q24.2 | 10q21.3 | |
Type of gene | protein-coding | protein-coding | |
Description | canalicular multispecific organic anion transporter 1ATP-binding cassette, sub-family C (CFTR/MRP), member 2canalicular multidrug resistance proteinmultidrug resistance-associated protein 2 | catenin alpha-3alpha-T-cateninalpha-catenin-like proteincatenin (cadherin-associated protein), alpha 3 | |
Modification date | 20200329 | 20200313 | |
UniProtAcc | . | Q9UI47 | |
Ensembl transtripts involved in fusion gene | ENST00000370434, ENST00000370449, ENST00000496621, | ||
Fusion gene scores | * DoF score | 3 X 3 X 2=18 | 23 X 20 X 6=2760 |
# samples | 3 | 25 | |
** MAII score | log2(3/18*10)=0.736965594166206 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(25/2760*10)=-3.46466826700344 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ABCC2 [Title/Abstract] AND CTNNA3 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | ABCC2(101544538)-CTNNA3(67680375), # samples:4 | ||
Anticipated loss of major functional domain due to fusion event. | ABCC2-CTNNA3 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. ABCC2-CTNNA3 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. ABCC2-CTNNA3 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF. ABCC2-CTNNA3 seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * 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 | LIHC | TCGA-DD-AAEA-01A | ABCC2 | chr10 | 101544538 | - | CTNNA3 | chr10 | 67680375 | - |
ChimerDB4 | LIHC | TCGA-DD-AAEA-01A | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
ChimerDB4 | LIHC | TCGA-DD-AAEA | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
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Fusion Gene ORF analysis for ABCC2-CTNNA3 |
![]() * 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 |
5CDS-5UTR | ENST00000370434 | ENST00000373735 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
5CDS-5UTR | ENST00000370449 | ENST00000373735 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
5CDS-intron | ENST00000370434 | ENST00000545309 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
5CDS-intron | ENST00000370449 | ENST00000545309 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
Frame-shift | ENST00000370434 | ENST00000433211 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
Frame-shift | ENST00000370449 | ENST00000433211 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
In-frame | ENST00000370434 | ENST00000373744 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
In-frame | ENST00000370449 | ENST00000373744 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
intron-3CDS | ENST00000496621 | ENST00000373744 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
intron-3CDS | ENST00000496621 | ENST00000433211 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
intron-5UTR | ENST00000496621 | ENST00000373735 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
intron-intron | ENST00000496621 | ENST00000545309 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - |
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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) |
ENST00000370449 | ABCC2 | chr10 | 101544538 | + | ENST00000373744 | CTNNA3 | chr10 | 67680375 | - | 919 | 320 | 113 | 607 | 164 |
ENST00000370434 | ABCC2 | chr10 | 101544538 | + | ENST00000373744 | CTNNA3 | chr10 | 67680375 | - | 888 | 289 | 82 | 576 | 164 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000370449 | ENST00000373744 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - | 0.05113019 | 0.9488698 |
ENST00000370434 | ENST00000373744 | ABCC2 | chr10 | 101544538 | + | CTNNA3 | chr10 | 67680375 | - | 0.06351676 | 0.93648326 |
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Fusion Genomic Features for ABCC2-CTNNA3 |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
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Fusion Protein Features for ABCC2-CTNNA3 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr10:101544538/chr10:67680375) - 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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Hgene | Tgene |
. | CTNNA3 |
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. | FUNCTION: May be involved in formation of stretch-resistant cell-cell adhesion complexes. {ECO:0000303|PubMed:11590244}. |
![]() * 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 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1_27 | 69 | 1546.0 | Topological domain | Extracellular |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 49_68 | 69 | 1546.0 | Topological domain | Cytoplasmic |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 28_48 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D1 |
- 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 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1300_1534 | 69 | 1546.0 | Domain | ABC transporter 2 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 322_605 | 69 | 1546.0 | Domain | ABC transmembrane type-1 1 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 637_861 | 69 | 1546.0 | Domain | ABC transporter 1 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 979_1264 | 69 | 1546.0 | Domain | ABC transmembrane type-1 2 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1334_1341 | 69 | 1546.0 | Nucleotide binding | ATP 2 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 671_678 | 69 | 1546.0 | Nucleotide binding | ATP 1 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1055_1097 | 69 | 1546.0 | Topological domain | Cytoplasmic |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1119_1119 | 69 | 1546.0 | Topological domain | Extracellular |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1141_1211 | 69 | 1546.0 | Topological domain | Cytoplasmic |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 115_126 | 69 | 1546.0 | Topological domain | Cytoplasmic |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1233_1234 | 69 | 1546.0 | Topological domain | Extracellular |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1256_1545 | 69 | 1546.0 | Topological domain | Cytoplasmic |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 148_165 | 69 | 1546.0 | Topological domain | Extracellular |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 187_313 | 69 | 1546.0 | Topological domain | Cytoplasmic |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 335_360 | 69 | 1546.0 | Topological domain | Extracellular |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 382_437 | 69 | 1546.0 | Topological domain | Cytoplasmic |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 459_461 | 69 | 1546.0 | Topological domain | Extracellular |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 483_544 | 69 | 1546.0 | Topological domain | Cytoplasmic |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 566_587 | 69 | 1546.0 | Topological domain | Extracellular |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 609_971 | 69 | 1546.0 | Topological domain | Cytoplasmic |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 90_93 | 69 | 1546.0 | Topological domain | Extracellular |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 993_1033 | 69 | 1546.0 | Topological domain | Extracellular |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1034_1054 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D13 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1098_1118 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D14 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1120_1140 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D15 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1212_1232 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D16 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 1235_1255 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D17 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 127_147 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D4 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 166_186 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D5 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 314_334 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D6 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 361_381 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D7 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 438_458 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D8 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 462_482 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D9 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 545_565 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D10 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 588_608 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D11 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 69_89 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D2 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 94_114 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D3 |
Hgene | ABCC2 | chr10:101544538 | chr10:67680375 | ENST00000370449 | + | 2 | 32 | 972_992 | 69 | 1546.0 | Transmembrane | Helical%3B Name%3D12 |
Tgene | CTNNA3 | chr10:101544538 | chr10:67680375 | ENST00000373744 | 15 | 17 | 325_379 | 800 | 896.0 | Coiled coil | Ontology_term=ECO:0000255 | |
Tgene | CTNNA3 | chr10:101544538 | chr10:67680375 | ENST00000373744 | 15 | 17 | 74_111 | 800 | 896.0 | Coiled coil | Ontology_term=ECO:0000255 | |
Tgene | CTNNA3 | chr10:101544538 | chr10:67680375 | ENST00000433211 | 16 | 18 | 325_379 | 800 | 896.0 | Coiled coil | Ontology_term=ECO:0000255 | |
Tgene | CTNNA3 | chr10:101544538 | chr10:67680375 | ENST00000433211 | 16 | 18 | 74_111 | 800 | 896.0 | Coiled coil | Ontology_term=ECO:0000255 |
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Fusion Gene Sequence for ABCC2-CTNNA3 |
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>245_245_1_ABCC2-CTNNA3_ABCC2_chr10_101544538_ENST00000370434_CTNNA3_chr10_67680375_ENST00000373744_length(transcript)=888nt_BP=289nt TTTCTTTGATGAAACAAGTAAAGAAGAAACAACACAATCATATTAATAGAAGAGTCTTCGTTCCAGACGCAGTCCAGGAATCATGCTGGA GAAGTTCTGCAACTCTACTTTTTGGAATTCCTCATTCCTGGACAGTCCGGAGGCAGACCTGCCACTTTGTTTTGAGCAAACTGTTCTGGT GTGGATTCCCTTGGGCTACCTATGGCTCCTGGCCCCCTGGCAGCTTCTCCACGTGTATAAATCCAGGACCAAGAGATCCTCTACCACCAA ACTCTATCTTGCTAAGCAGTTGGACAGTGTCACATCCCTGATCCAAGCAGCCAAAAATTTAATGAATGCTGTAGTGCAAACAGTGAAAAT GTCTTACATTGCCTCAACCAAGATCATCCGAATCCAGAGTCCTGCTGGGCCCCGGCACCCAGTTGTGATGTGGAGAATGAAGGCTCCTGC AAAAAAACCCTTGATTAAAAGAGAGAAGCCAGAGGAAACGTGTGCAGCTGTCAGACGAGGCTCAGCAAAGAAAAAAATCCATCCATTGCA AGTCATGAGTGAATTTAGAGGAAGACAAATCTACTGAAACCACTATTCTACATATAGTGCCTATATGACAAAATCCTGCCTAACCACACT GCTTTATTTTACACTTAAGAAGTTCTGTAATTTCACTAAGTTTTGGTGTTTAACTCACAAATAACATAAAATATTGGGCGCTAAATCAAC AAAAGCAATATATATTTGGGATCATATCACTGTCATTTCTGTATGGTCAGCACCTAATAGTTAAGGAATATTTGCTTGTTGAATGAATGA >245_245_1_ABCC2-CTNNA3_ABCC2_chr10_101544538_ENST00000370434_CTNNA3_chr10_67680375_ENST00000373744_length(amino acids)=164AA_BP=68 MLEKFCNSTFWNSSFLDSPEADLPLCFEQTVLVWIPLGYLWLLAPWQLLHVYKSRTKRSSTTKLYLAKQLDSVTSLIQAAKNLMNAVVQT -------------------------------------------------------------- >245_245_2_ABCC2-CTNNA3_ABCC2_chr10_101544538_ENST00000370449_CTNNA3_chr10_67680375_ENST00000373744_length(transcript)=919nt_BP=320nt ACATCAGAATGGTAGATAATTCCTGTTCCACTTTCTTTGATGAAACAAGTAAAGAAGAAACAACACAATCATATTAATAGAAGAGTCTTC GTTCCAGACGCAGTCCAGGAATCATGCTGGAGAAGTTCTGCAACTCTACTTTTTGGAATTCCTCATTCCTGGACAGTCCGGAGGCAGACC TGCCACTTTGTTTTGAGCAAACTGTTCTGGTGTGGATTCCCTTGGGCTACCTATGGCTCCTGGCCCCCTGGCAGCTTCTCCACGTGTATA AATCCAGGACCAAGAGATCCTCTACCACCAAACTCTATCTTGCTAAGCAGTTGGACAGTGTCACATCCCTGATCCAAGCAGCCAAAAATT TAATGAATGCTGTAGTGCAAACAGTGAAAATGTCTTACATTGCCTCAACCAAGATCATCCGAATCCAGAGTCCTGCTGGGCCCCGGCACC CAGTTGTGATGTGGAGAATGAAGGCTCCTGCAAAAAAACCCTTGATTAAAAGAGAGAAGCCAGAGGAAACGTGTGCAGCTGTCAGACGAG GCTCAGCAAAGAAAAAAATCCATCCATTGCAAGTCATGAGTGAATTTAGAGGAAGACAAATCTACTGAAACCACTATTCTACATATAGTG CCTATATGACAAAATCCTGCCTAACCACACTGCTTTATTTTACACTTAAGAAGTTCTGTAATTTCACTAAGTTTTGGTGTTTAACTCACA AATAACATAAAATATTGGGCGCTAAATCAACAAAAGCAATATATATTTGGGATCATATCACTGTCATTTCTGTATGGTCAGCACCTAATA GTTAAGGAATATTTGCTTGTTGAATGAATGAAATTATCACGTGTCATTCAGCGTTTCCCATCATAGAGATTATCTACTATTCGTTACCAA >245_245_2_ABCC2-CTNNA3_ABCC2_chr10_101544538_ENST00000370449_CTNNA3_chr10_67680375_ENST00000373744_length(amino acids)=164AA_BP=68 MLEKFCNSTFWNSSFLDSPEADLPLCFEQTVLVWIPLGYLWLLAPWQLLHVYKSRTKRSSTTKLYLAKQLDSVTSLIQAAKNLMNAVVQT -------------------------------------------------------------- |
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Fusion Gene PPI Analysis for ABCC2-CTNNA3 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for ABCC2-CTNNA3 |
![]() (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 ABCC2-CTNNA3 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ABCC2 | C0022350 | Jaundice, Chronic Idiopathic | 11 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Hgene | ABCC2 | C0008370 | Cholestasis | 5 | CTD_human;GENOMICS_ENGLAND |
Hgene | ABCC2 | C0013221 | Drug toxicity | 3 | CTD_human |
Hgene | ABCC2 | C0041755 | Adverse reaction to drug | 3 | CTD_human |
Hgene | ABCC2 | C0019193 | Hepatitis, Toxic | 2 | CTD_human |
Hgene | ABCC2 | C0268318 | Cholestasis of pregnancy | 2 | GENOMICS_ENGLAND |
Hgene | ABCC2 | C0860207 | Drug-Induced Liver Disease | 2 | CTD_human |
Hgene | ABCC2 | C1262760 | Hepatitis, Drug-Induced | 2 | CTD_human |
Hgene | ABCC2 | C3658290 | Drug-Induced Acute Liver Injury | 2 | CTD_human |
Hgene | ABCC2 | C4277682 | Chemical and Drug Induced Liver Injury | 2 | CTD_human |
Hgene | ABCC2 | C4279912 | Chemically-Induced Liver Toxicity | 2 | CTD_human |
Hgene | ABCC2 | C0002170 | Alopecia | 1 | CTD_human |
Hgene | ABCC2 | C0003873 | Rheumatoid Arthritis | 1 | CTD_human |
Hgene | ABCC2 | C0008312 | Primary biliary cirrhosis | 1 | CTD_human |
Hgene | ABCC2 | C0009402 | Colorectal Carcinoma | 1 | CTD_human |
Hgene | ABCC2 | C0009404 | Colorectal Neoplasms | 1 | CTD_human |
Hgene | ABCC2 | C0013182 | Drug Allergy | 1 | CTD_human |
Hgene | ABCC2 | C0017178 | Gastrointestinal Diseases | 1 | CTD_human |
Hgene | ABCC2 | C0018799 | Heart Diseases | 1 | CTD_human |
Hgene | ABCC2 | C0020433 | Hyperbilirubinemia | 1 | CTD_human |
Hgene | ABCC2 | C0022333 | Jacksonian Seizure | 1 | CTD_human |
Hgene | ABCC2 | C0023892 | Biliary cirrhosis | 1 | CTD_human |
Hgene | ABCC2 | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
Hgene | ABCC2 | C0027765 | nervous system disorder | 1 | CTD_human |
Hgene | ABCC2 | C0036572 | Seizures | 1 | CTD_human |
Hgene | ABCC2 | C0038220 | Status Epilepticus | 1 | CTD_human |
Hgene | ABCC2 | C0086873 | Pseudopelade | 1 | CTD_human |
Hgene | ABCC2 | C0149958 | Complex partial seizures | 1 | CTD_human |
Hgene | ABCC2 | C0162311 | Androgenetic Alopecia | 1 | CTD_human |
Hgene | ABCC2 | C0234533 | Generalized seizures | 1 | CTD_human |
Hgene | ABCC2 | C0234535 | Clonic Seizures | 1 | CTD_human |
Hgene | ABCC2 | C0238065 | Secondary Biliary Cholangitis | 1 | CTD_human |
Hgene | ABCC2 | C0263477 | Female pattern alopecia (disorder) | 1 | CTD_human |
Hgene | ABCC2 | C0270823 | Petit mal status | 1 | CTD_human |
Hgene | ABCC2 | C0270824 | Visual seizure | 1 | CTD_human |
Hgene | ABCC2 | C0270844 | Tonic Seizures | 1 | CTD_human |
Hgene | ABCC2 | C0270846 | Epileptic drop attack | 1 | CTD_human |
Hgene | ABCC2 | C0279626 | Squamous cell carcinoma of esophagus | 1 | CTD_human |
Hgene | ABCC2 | C0311335 | Grand Mal Status Epilepticus | 1 | CTD_human |
Hgene | ABCC2 | C0393734 | Complex Partial Status Epilepticus | 1 | CTD_human |
Hgene | ABCC2 | C0400966 | Non-alcoholic Fatty Liver Disease | 1 | CTD_human |
Hgene | ABCC2 | C0422850 | Seizures, Somatosensory | 1 | CTD_human |
Hgene | ABCC2 | C0422852 | Seizures, Auditory | 1 | CTD_human |
Hgene | ABCC2 | C0422853 | Olfactory seizure | 1 | CTD_human |
Hgene | ABCC2 | C0422854 | Gustatory seizure | 1 | CTD_human |
Hgene | ABCC2 | C0422855 | Vertiginous seizure | 1 | CTD_human |
Hgene | ABCC2 | C0494475 | Tonic - clonic seizures | 1 | CTD_human |
Hgene | ABCC2 | C0559031 | Functional Gastrointestinal Disorders | 1 | CTD_human |
Hgene | ABCC2 | C0751056 | Non-epileptic convulsion | 1 | CTD_human |
Hgene | ABCC2 | C0751110 | Single Seizure | 1 | CTD_human |
Hgene | ABCC2 | C0751123 | Atonic Absence Seizures | 1 | CTD_human |
Hgene | ABCC2 | C0751494 | Convulsive Seizures | 1 | CTD_human |
Hgene | ABCC2 | C0751495 | Seizures, Focal | 1 | CTD_human |
Hgene | ABCC2 | C0751496 | Seizures, Sensory | 1 | CTD_human |
Hgene | ABCC2 | C0751522 | Status Epilepticus, Subclinical | 1 | CTD_human |
Hgene | ABCC2 | C0751523 | Non-Convulsive Status Epilepticus | 1 | CTD_human |
Hgene | ABCC2 | C0751524 | Simple Partial Status Epilepticus | 1 | CTD_human |
Hgene | ABCC2 | C1168401 | Squamous cell carcinoma of the head and neck | 1 | CTD_human |
Hgene | ABCC2 | C1565321 | Cholera Infantum | 1 | CTD_human |
Hgene | ABCC2 | C3241937 | Nonalcoholic Steatohepatitis | 1 | CTD_human |
Hgene | ABCC2 | C3495874 | Nonepileptic Seizures | 1 | CTD_human |
Hgene | ABCC2 | C4048158 | Convulsions | 1 | CTD_human |
Hgene | ABCC2 | C4083212 | Alopecia, Male Pattern | 1 | CTD_human |
Hgene | ABCC2 | C4316903 | Absence Seizures | 1 | CTD_human |
Hgene | ABCC2 | C4317109 | Epileptic Seizures | 1 | CTD_human |
Hgene | ABCC2 | C4317123 | Myoclonic Seizures | 1 | CTD_human |
Hgene | ABCC2 | C4505436 | Generalized Absence Seizures | 1 | CTD_human |
Hgene | ABCC2 | C4551595 | Biliary Cirrhosis, Primary, 1 | 1 | CTD_human |
Tgene | C0004096 | Asthma | 1 | CTD_human | |
Tgene | C0013146 | Drug abuse | 1 | CTD_human | |
Tgene | C0013170 | Drug habituation | 1 | CTD_human | |
Tgene | C0013222 | Drug Use Disorders | 1 | CTD_human | |
Tgene | C0029231 | Organic Mental Disorders, Substance-Induced | 1 | CTD_human | |
Tgene | C0038580 | Substance Dependence | 1 | CTD_human | |
Tgene | C0038586 | Substance Use Disorders | 1 | CTD_human | |
Tgene | C0236969 | Substance-Related Disorders | 1 | CTD_human | |
Tgene | C0740858 | Substance abuse problem | 1 | CTD_human | |
Tgene | C1510472 | Drug Dependence | 1 | CTD_human | |
Tgene | C1832931 | ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2 | 1 | ORPHANET | |
Tgene | C3810138 | ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13 | 1 | CTD_human;GENOMICS_ENGLAND;UNIPROT | |
Tgene | C4316881 | Prescription Drug Abuse | 1 | CTD_human |