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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:AHCY-PIGU (FusionGDB2 ID:HG191TG128869)

Fusion Gene Summary for AHCY-PIGU

check button Fusion gene summary
Fusion gene informationFusion gene name: AHCY-PIGU
Fusion gene ID: hg191tg128869
HgeneTgene
Gene symbol

AHCY

PIGU

Gene ID

191

128869

Gene nameadenosylhomocysteinasephosphatidylinositol glycan anchor biosynthesis class U
SynonymsSAHH|adoHcyaseCDC91L1|GAB1|GPIBD21
Cytomap('AHCY')('PIGU')

20q11.22

20q11.22

Type of geneprotein-codingprotein-coding
DescriptionadenosylhomocysteinaseS-adenosyl-L-homocysteine hydrolaseS-adenosylhomocysteine hydrolaseepididymis secretory sperm binding proteinphosphatidylinositol glycan anchor biosynthesis class U proteinCDC91 (cell division cycle 91, S. cerevisiae, homolog)-like 1GPI transamidase component PIG-UGPI transamidase subunitcell division cycle 91-like 1 proteincell division cycle protein 91-li
Modification date2020032020200322
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000217426, ENST00000538132, 
ENST00000468908, 
ENST00000468908, 
ENST00000217426, ENST00000538132, 
Fusion gene scores* DoF score9 X 9 X 4=32419 X 15 X 11=3135
# samples 921
** MAII scorelog2(9/324*10)=-1.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(21/3135*10)=-3.90000421002328
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: AHCY [Title/Abstract] AND PIGU [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointAHCY(32881886)-PIGU(33245048), # samples:1
Anticipated loss of major functional domain due to fusion event.AHCY-PIGU 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.
AHCY-PIGU 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.
PIGU-AHCY 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.
PIGU-AHCY 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.
AHCY-PIGU seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
AHCY-PIGU seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
AHCY-PIGU seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
AHCY-PIGU seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
AHCY-PIGU seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
PIGU-AHCY seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PIGU-AHCY seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
PIGU-AHCY seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
PIGU-AHCY seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
PIGU-AHCY seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
TgenePIGU

GO:0006506

GPI anchor biosynthetic process

15034568

TgenePIGU

GO:0046425

regulation of JAK-STAT cascade

15034568


check buttonFusion gene breakpoints across AHCY (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure
check buttonFusion gene breakpoints across PIGU (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check button Fusion gene information
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4STADTCGA-HU-A4GXAHCYchr20

32881886

-PIGUchr20

33245048

-


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Fusion Gene ORF analysis for AHCY-PIGU

check button 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.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5CDS-intronENST00000217426ENST00000480175AHCYchr20

32881886

-PIGUchr20

33245048

-
5CDS-intronENST00000538132ENST00000480175AHCYchr20

32881886

-PIGUchr20

33245048

-
5UTR-3CDSENST00000468908ENST00000374820AHCYchr20

32881886

-PIGUchr20

33245048

-
5UTR-3CDSENST00000468908ENST00000452740AHCYchr20

32881886

-PIGUchr20

33245048

-
5UTR-intronENST00000468908ENST00000480175AHCYchr20

32881886

-PIGUchr20

33245048

-
Frame-shiftENST00000217426ENST00000452740AHCYchr20

32881886

-PIGUchr20

33245048

-
Frame-shiftENST00000538132ENST00000374820AHCYchr20

32881886

-PIGUchr20

33245048

-
In-frameENST00000217426ENST00000374820AHCYchr20

32881886

-PIGUchr20

33245048

-
In-frameENST00000538132ENST00000452740AHCYchr20

32881886

-PIGUchr20

33245048

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000538132AHCYchr2032881886-ENST00000452740PIGUchr2033245048-19375982461739497
ENST00000217426AHCYchr2032881886-ENST00000374820PIGUchr2033245048-1814373781490470

check buttonDeepORF 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.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000538132ENST00000452740AHCYchr2032881886-PIGUchr2033245048-0.0212811940.9787188
ENST00000217426ENST00000374820AHCYchr2032881886-PIGUchr2033245048-0.0074740410.99252594

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Fusion Genomic Features for AHCY-PIGU


check buttonFusionAI 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.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution 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.
genomic feature

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Fusion Protein Features for AHCY-PIGU


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr20:32881886/chr20:33245048)
- 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.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
..
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: 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}.

check buttonRetention 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

download page


* 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.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgenePIGUchr20:32881886chr20:33245048ENST00000374820011269_28943416.0RegionNote=May be involved in recognition of long-chain fatty acids in GPI
TgenePIGUchr20:32881886chr20:33245048ENST00000374820011166_18643416.0TransmembraneHelical
TgenePIGUchr20:32881886chr20:33245048ENST00000374820011188_20843416.0TransmembraneHelical
TgenePIGUchr20:32881886chr20:33245048ENST00000374820011237_25743416.0TransmembraneHelical
TgenePIGUchr20:32881886chr20:33245048ENST00000374820011259_27943416.0TransmembraneHelical
TgenePIGUchr20:32881886chr20:33245048ENST00000374820011286_30643416.0TransmembraneHelical
TgenePIGUchr20:32881886chr20:33245048ENST00000374820011313_33343416.0TransmembraneHelical
TgenePIGUchr20:32881886chr20:33245048ENST00000374820011355_37543416.0TransmembraneHelical
TgenePIGUchr20:32881886chr20:33245048ENST00000374820011386_40643416.0TransmembraneHelical
TgenePIGUchr20:32881886chr20:33245048ENST0000037482001166_8643416.0TransmembraneHelical

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneAHCYchr20:32881886chr20:33245048ENST00000217426-310157_15998433.0Nucleotide bindingNAD
HgeneAHCYchr20:32881886chr20:33245048ENST00000217426-310222_22798433.0Nucleotide bindingNAD
HgeneAHCYchr20:32881886chr20:33245048ENST00000217426-310299_30198433.0Nucleotide bindingNAD
HgeneAHCYchr20:32881886chr20:33245048ENST00000538132-310157_15970405.0Nucleotide bindingNAD
HgeneAHCYchr20:32881886chr20:33245048ENST00000538132-310222_22770405.0Nucleotide bindingNAD
HgeneAHCYchr20:32881886chr20:33245048ENST00000538132-310299_30170405.0Nucleotide bindingNAD


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Fusion Gene Sequence for AHCY-PIGU


check button 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.
>3071_3071_1_AHCY-PIGU_AHCY_chr20_32881886_ENST00000217426_PIGU_chr20_33245048_ENST00000374820_length(transcript)=1814nt_BP=373nt
CGGCGCTGCCCGCCCAGTTCCTGTTCCCAGACTGAGGCCCAGCCCCCTTCGCCCGTTTCCATCACGAGTGCCGCCAGCATGTCTGACAAA
CTGCCCTACAAAGTCGCCGACATCGGCCTGGCTGCCTGGGGACGCAAGGCCCTGGACATTGCTGAGAACGAGATGCCGGGCCTGATGCGT
ATGCGGGAGCGGTACTCGGCCTCCAAGCCACTGAAGGGCGCCCGCATCGCTGGCTGCCTGCACATGACCGTGGAGACGGCCGTCCTCATT
GAGACCCTCGTCACCCTGGGTGCTGAGGTGCAGTGGTCCAGCTGCAACATCTTCTCCACCCAGGACCATGCGGCGGCTGCCATTGCCAAG
GCTGGCATTCCGGTGGTTGAAGGCCTTTCACTGTTGGACTTGGGAGTATCTCCGTATTCTGGAGCAGTATTTCATGAAATAACTGATGCA
CTCACTGCTATTGCCCTGTATTTTGCAATCCAGGACTTCAATAAAGTTGTGTTTAAAAAGCAGAAACTCCTCCTAGAACTGGACCAGTAT
GCCCCAGATGTGGCCGAACTCATCCGGACCCCTATGGAAATGCGTTACATCCCTTTGAAAGTGGCCCTGTTCTATCTCTTAAATCCTTAC
ACGATTTTGTCTTGTGTTGCCAAGTCTACCTGTGCCATCAACAACACCCTCATTGCTTTCTTCATTTTGACTACGATAAAAGGCAGTGCT
TTCCTCAGTGCTATTTTTCTTGCCTTAGCGACATACCAGTCTCTGTACCCACTCACCTTGTTTGTCCCAGGACTCCTCTATCTCCTCCAG
CGGCAGTACATACCTGTGAAAATGAAGAGCAAAGCCTTCTGGATCTTTTCTTGGGAGTATGCCATGATGTATGTGGGAAGCCTAGTGGTA
ATCATTTGCCTCTCCTTCTTCCTTCTCAGCTCTTGGGATTTCATCCCCGCAGTCTATGGCTTTATACTTTCTGTTCCAGATCTCACTCCA
AACATTGGTCTTTTCTGGTACTTCTTTGCAGAGATGTTTGAGCACTTCAGCCTCTTCTTTGTATGTGTGTTTCAGATCAACGTCTTCTTC
TACACCATCCCCTTAGCCATAAAGCTAAAGGAGCACCCCATCTTCTTCATGTTTATCCAGATCGCTGTCATCGCCATCTTTAAGTCCTAC
CCGACAGTGGGGGACGTGGCGCTCTACATGGCCTTCTTCCCCGTGTGGAACCATCTCTACAGATTCCTGAGAAACATCTTTGTCCTCACC
TGCATCATCATCGTCTGTTCCCTGCTCTTCCCTGTCCTGTGGCACCTCTGGATTTATGCAGGAAGTGCCAACTCTAATTTCTTTTATGCC
ATCACACTGACCTTCAACGTTGGGCAGATCCTGCTCATCTCTGATTACTTCTATGCCTTCCTGCGGCGGGAGTACTACCTCACACATGGC
CTCTACTTGACCGCCAAGGATGGCACAGAGGCCATGCTCGTGCTCAAGTAGGCCTGGCTGGCACAGGGCTGCATGGACCTCAGGGGGCTG
TGGGGCCAGAAGCTGGGCCAAGCCCTCCAGCCAGAGTTGCCAGCAGGCGAGTGCTTGGGCAGAAGAGGTTCGAGTCCAGGGTCACAAGTC
TCTGGTACCAAAAGGGACCCATGGCTGACTGACAGCAAGGCCTATGGGGAAGAACTGGGAGCTCCCCAACTTGGACCCCCACCTTGTGGC
TCTGCACACCAAGGAGCCCCCTCCCAGACAGGAAGGAGAAGAGGCAGGTGAGCAGGGCTTGTTAGATTGTGGCTACTTAATAAATGTTTT
TTGTTATGAAGTCT

>3071_3071_1_AHCY-PIGU_AHCY_chr20_32881886_ENST00000217426_PIGU_chr20_33245048_ENST00000374820_length(amino acids)=470AA_BP=98
MSDKLPYKVADIGLAAWGRKALDIAENEMPGLMRMRERYSASKPLKGARIAGCLHMTVETAVLIETLVTLGAEVQWSSCNIFSTQDHAAA
AIAKAGIPVVEGLSLLDLGVSPYSGAVFHEITDALTAIALYFAIQDFNKVVFKKQKLLLELDQYAPDVAELIRTPMEMRYIPLKVALFYL
LNPYTILSCVAKSTCAINNTLIAFFILTTIKGSAFLSAIFLALATYQSLYPLTLFVPGLLYLLQRQYIPVKMKSKAFWIFSWEYAMMYVG
SLVVIICLSFFLLSSWDFIPAVYGFILSVPDLTPNIGLFWYFFAEMFEHFSLFFVCVFQINVFFYTIPLAIKLKEHPIFFMFIQIAVIAI
FKSYPTVGDVALYMAFFPVWNHLYRFLRNIFVLTCIIIVCSLLFPVLWHLWIYAGSANSNFFYAITLTFNVGQILLISDYFYAFLRREYY
LTHGLYLTAKDGTEAMLVLK

--------------------------------------------------------------
>3071_3071_2_AHCY-PIGU_AHCY_chr20_32881886_ENST00000538132_PIGU_chr20_33245048_ENST00000452740_length(transcript)=1937nt_BP=598nt
CTGGAGGGAGGGGCGTGGATACAGCGGGAAAGGAGAGACCCCTAGCGGGGTGGACAAGAAGGGAGGAACTCCACAGAACTGCTTAATCCG
GCTCCATCCCCATCAGCGGGCTTTCTCAGCGCCTGCACCCCTCTCTATCCCATCTCGAAGCCTCCAGTTAATCCAGAGTGAGACGCAGGA
CCGCCGGGAGGCGAGCGGGGATGCTGAAGCTAGGGCAGGCTAAAGCCCCGCGGCCAAAGGGCAGGCTTGTGCGCCCTCCGCCCCCTCTCC
GCCCCCTCTCCGCCCCTCCGCGCCCAGGACCTAATTGTTTGCAAAAGCAAACACGGAAAAGCCGACATCGGCCTGGCTGCCTGGGGACGC
AAGGCCCTGGACATTGCTGAGAACGAGATGCCGGGCCTGATGCGTATGCGGGAGCGGTACTCGGCCTCCAAGCCACTGAAGGGCGCCCGC
ATCGCTGGCTGCCTGCACATGACCGTGGAGACGGCCGTCCTCATTGAGACCCTCGTCACCCTGGGTGCTGAGGTGCAGTGGTCCAGCTGC
AACATCTTCTCCACCCAGGACCATGCGGCGGCTGCCATTGCCAAGGCTGGCATTCCGGTGGTTGAAGGCCTTTCACTGTTGGACTTGGGA
GTATCTCCGTATTCTGGAGCAGTATTTCATGAAACTCCATTAATAATATACCTCTTTCATTTCCTAATTGACTATGCTGAATTGGTGTTT
ATGATAACTGATGCACTCACTGCTATTGCCCTGTATTTTGCAATCCAGGACTTCAATAAAGTTGTGTTTAAAAAGCAGAAACTCCTCCTA
GAACTGGACCAGTATGCCCCAGATGTGGCCGAACTCATCCGGACCCCTATGGAAATGCGTTACATCCCTTTGAAAGTGGCCCTGTTCTAT
CTCTTAAATCCTTACACGATTTTGTCTTGTGTTGCCAAGTCTACCTGTGCCATCAACAACACCCTCATTGCTTTCTTCATTTTGACTACG
ATAAAAGGCAGTGCTTTCCTCAGTGCTATTTTTCTTGCCTTAGCGACATACCAGTCTCTGTACCCACTCACCTTGTTTGTCCCAGGACTC
CTCTATCTCCTCCAGCGGCAGTACATACCTGTGAAAATGAAGAGCAAAGCCTTCTGGATCTTTTCTTGGGAGTATGCCATGATGTATGTG
GGAAGCCTAGTGGTAATCATTTGCCTCTCCTTCTTCCTTCTCAGCTCTTGGGATTTCATCCCCGCAGTCTATGGCTTTATACTTTCTGTT
CCAGATCTCACTCCAAACATTGGTCTTTTCTGGTACTTCTTTGCAGAGATGTTTGAGCACTTCAGCCTCTTCTTTGTATGTGTGTTTCAG
ATCAACGTCTTCTTCTACACCATCCCCTTAGCCATAAAGCTAAAGGAGCACCCCATCTTCTTCATGTTTATCCAGATCGCTGTCATCGCC
ATCTTTAAGTCCTACCCGACAGTGGGGGACGTGGCGCTCTACATGGCCTTCTTCCCCGTGTGGAACCATCTCTACAGATTCCTGAGAAAC
ATCTTTGTCCTCACCTGCATCATCATCGTCTGTTCCCTGCTCTTCCCTGTCCTGTGGCACCTCTGGATTTATGCAGGAAGTGCCAACTCT
AATTTCTTTTATGCCATCACACTGACCTTCAACGTTGGGCAGATGGGCTTCTGTGGTGATAGAATGGCAGGTACTTGTCCTGAGGCCATC
AGAGCTGCTGGTGACAGGACACCTTCCTGAACTCCTCCAGGCGCCTCTGATCTCTCCTTAGCTGCTGTTGTGTTACCTTCAGATCCTGCT
CATCTCTGATTACTTCTATGCCTTCCTGCGGCGGGAGTACTACCTCACACATGGCCTCTACTTGACCGCCAAGGATGGCACAGAGGCCAT
GCTCGTGCTCAAGTAGGCCTGGCTGGCACAGGGCTGCATGGACCTCA

>3071_3071_2_AHCY-PIGU_AHCY_chr20_32881886_ENST00000538132_PIGU_chr20_33245048_ENST00000452740_length(amino acids)=497AA_BP=117
MCALRPLSAPSPPLRAQDLIVCKSKHGKADIGLAAWGRKALDIAENEMPGLMRMRERYSASKPLKGARIAGCLHMTVETAVLIETLVTLG
AEVQWSSCNIFSTQDHAAAAIAKAGIPVVEGLSLLDLGVSPYSGAVFHETPLIIYLFHFLIDYAELVFMITDALTAIALYFAIQDFNKVV
FKKQKLLLELDQYAPDVAELIRTPMEMRYIPLKVALFYLLNPYTILSCVAKSTCAINNTLIAFFILTTIKGSAFLSAIFLALATYQSLYP
LTLFVPGLLYLLQRQYIPVKMKSKAFWIFSWEYAMMYVGSLVVIICLSFFLLSSWDFIPAVYGFILSVPDLTPNIGLFWYFFAEMFEHFS
LFFVCVFQINVFFYTIPLAIKLKEHPIFFMFIQIAVIAIFKSYPTVGDVALYMAFFPVWNHLYRFLRNIFVLTCIIIVCSLLFPVLWHLW
IYAGSANSNFFYAITLTFNVGQMGFCGDRMAGTCPEAIRAAGDRTPS

--------------------------------------------------------------

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Fusion Gene PPI Analysis for AHCY-PIGU


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for AHCY-PIGU


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for AHCY-PIGU


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneAHCYC3151058S-adenosylhomocysteine hydrolase deficiency13CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneAHCYC4510276Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency10CLINGEN
HgeneAHCYC0002514Amino Acid Metabolism, Inborn Errors1CTD_human
HgeneAHCYC0003129Anoxemia1CTD_human
HgeneAHCYC0003130Anoxia1CTD_human
HgeneAHCYC0019202Hepatolenticular Degeneration1CTD_human
HgeneAHCYC0152013Adenocarcinoma of lung (disorder)1CTD_human
HgeneAHCYC0242184Hypoxia1CTD_human
HgeneAHCYC0268621Hepatic methionine adenosyltransferase deficiency1CTD_human
HgeneAHCYC0400966Non-alcoholic Fatty Liver Disease1CTD_human
HgeneAHCYC0700292Hypoxemia1CTD_human
HgeneAHCYC0750905Amino Acid Metabolism, Inherited Disorders1CTD_human
HgeneAHCYC1527352Hepatic Form of Wilson Disease1CTD_human
HgeneAHCYC1847720Hypermethioninemia due to deficiency of glycine N-methyltransferase1CTD_human
HgeneAHCYC3241937Nonalcoholic Steatohepatitis1CTD_human
HgeneAHCYC4048705Hypermethioninemia1CTD_human
TgeneC0036439Scoliosis, unspecified1GENOMICS_ENGLAND
TgeneC0036572Seizures1GENOMICS_ENGLAND
TgeneC0235946Cerebral atrophy1GENOMICS_ENGLAND
TgeneC0266470Cerebellar Hypoplasia1GENOMICS_ENGLAND
TgeneC0557874Global developmental delay1GENOMICS_ENGLAND
TgeneC3714756Intellectual Disability1GENOMICS_ENGLAND
TgeneC4023501Focal myoclonic seizures1GENOMICS_ENGLAND
TgeneC4317123Myoclonic Seizures1GENOMICS_ENGLAND