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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:PLEKHG1-DTYMK (FusionGDB2 ID:66259)

Fusion Gene Summary for PLEKHG1-DTYMK

check button Fusion gene summary
Fusion gene informationFusion gene name: PLEKHG1-DTYMK
Fusion gene ID: 66259
HgeneTgene
Gene symbol

PLEKHG1

DTYMK

Gene ID

57480

1841

Gene namepleckstrin homology and RhoGEF domain containing G1deoxythymidylate kinase
SynonymsARHGEF41CDC8|PP3731|TMPK|TYMK
Cytomap

6q25.1

2q37.3

Type of geneprotein-codingprotein-coding
Descriptionpleckstrin homology domain-containing family G member 1pleckstrin homology domain containing, family G (with RhoGef domain) member 1thymidylate kinasedTMP kinasedeoxythymidylate kinase (thymidylate kinase)
Modification date2020031320200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000358517, ENST00000367328, 
ENST00000493095, ENST00000305784, 
Fusion gene scores* DoF score11 X 11 X 10=12105 X 3 X 4=60
# samples 195
** MAII scorelog2(19/1210*10)=-2.67093572383101
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PLEKHG1 [Title/Abstract] AND DTYMK [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointPLEKHG1(151140910)-DTYMK(242625292), # 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)

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

check buttonFusion gene breakpoints across PLEKHG1 (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 DTYMK (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 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4SKCMTCGA-DA-A1I0-06APLEKHG1chr6

151140910

+DTYMKchr2

242625292

-


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Fusion Gene ORF analysis for PLEKHG1-DTYMK

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-5UTRENST00000358517ENST00000493095PLEKHG1chr6

151140910

+DTYMKchr2

242625292

-
5CDS-5UTRENST00000367328ENST00000493095PLEKHG1chr6

151140910

+DTYMKchr2

242625292

-
In-frameENST00000358517ENST00000305784PLEKHG1chr6

151140910

+DTYMKchr2

242625292

-
In-frameENST00000367328ENST00000305784PLEKHG1chr6

151140910

+DTYMKchr2

242625292

-

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)
ENST00000367328PLEKHG1chr6151140910+ENST00000305784DTYMKchr2242625292-261417202252228667
ENST00000358517PLEKHG1chr6151140910+ENST00000305784DTYMKchr2242625292-25131619552127690

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
ENST00000367328ENST00000305784PLEKHG1chr6151140910+DTYMKchr2242625292-0.0070530970.9929469
ENST00000358517ENST00000305784PLEKHG1chr6151140910+DTYMKchr2242625292-0.0063354950.9936645

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Fusion Genomic Features for PLEKHG1-DTYMK


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

check buttonDistribution 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 PLEKHG1-DTYMK


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/chr6:151140910/chr2:242625292)
- 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
HgenePLEKHG1chr6:151140910chr2:242625292ENST00000358517+1216113_2934691386.0DomainDH
HgenePLEKHG1chr6:151140910chr2:242625292ENST00000358517+1216317_4164691386.0DomainPH
HgenePLEKHG1chr6:151140910chr2:242625292ENST00000367328+1317113_2934691386.0DomainDH
HgenePLEKHG1chr6:151140910chr2:242625292ENST00000367328+1317317_4164691386.0DomainPH

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneDTYMKchr6:151140910chr2:242625292ENST000003057840513_2043213.0Nucleotide bindingATP


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Fusion Gene Sequence for PLEKHG1-DTYMK


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.
>66259_66259_1_PLEKHG1-DTYMK_PLEKHG1_chr6_151140910_ENST00000358517_DTYMK_chr2_242625292_ENST00000305784_length(transcript)=2513nt_BP=1619nt
AATATTTCTACGGAAGGCGCTGCACAGACTAGCAAAGGCTGTTTCTTTTACCTGACTGAGGTCACTGCATCAGCTGAAGGCAGACGATGT
GCTTAAGCCTGAGTGGAGCAGAGATGGGCACCAGTTGCGTCTTGAAGTGCCATCAGCTGTAACCAAAGTTCCACATCCCAAGACGACAGC
CAGGCGTTCCTGCCCTCAAGAACTGAAGACAATGGAGCTCTCTGATAGTGACCGACCCGTCAGCTTCGGTTCCACATCATCCTCGGCCTC
TTCCCGCGACAGCCATGGTTCCTTCGGCAGCAGAATGACCTTAGTTTCAAATAGCCACATGGGCTTGTTTAACCAGGATAAGGAGGTAGG
GGCCATAAAACTGGAGCTGATTCCTGCCAGGCCGTTTTCCAGCAGCGAGCTGCAGAGGGACAACCCCGCCACGGGGCAACAGAACGCGGA
TGAGGGCAGCGAAAGGCCACCCAGAGCGCAGTGGAGAGTGGACTCAAACGGGGCACCCAAGACGATCGCAGACTCGGCCACGAGCCCCAA
GCTCCTCTATGTGGATAGAGTTGTTCAGGAAATTCTGGAAACCGAAAGGACTTATGTACAAGATTTAAAAAGCATCGTAGAGGATTACCT
TGACTGCATCAGGGACCAAACAAAACTTCCCCTGGGGACCGAAGAAAGATCAGCCCTTTTTGGAAACATACAGGATATCTACCACTTCAA
TAGTGAACTTCTGCAAGATTTGGAAAACTGTGAAAATGATCCTGTGGCCATAGCAGAGTGTTTTGTGTCCAAGAGTGAAGAGTTCCACAT
TTATACCCAGTATTGCACTAACTATCCAAGGTCCGTGGCTGTGCTAACAGAGTGTATGAGGAACAAGATACTGGCCAAATTCTTCAGGGA
GCGTCAGGAAACTCTGAAACACTCGCTGCCTCTGGGGTCCTATCTCTTGAAACCAGTTCAGCGGATTCTCAAGTATCATCTCCTTCTGCA
TGAAATAGAAAACCACCTTGATAAGGACACAGAAGGCTATGATGTGGTGCTTGATGCTATAGACACAATGCAGCGAGTCGCCTGGCATAT
CAATGACATGAAGCGGAAACACGAGCACGCGGTCCGGTTACAGGAGATACAGAGTTTGCTCACTAACTGGAAGGGGCCAGACCTGACCAG
CTACGGGGAACTGGTGCTTGAGGGAACCTTCCGCATCCAGCGAGCCAAGAATGAGCGGACGCTCTTCCTCTTCGACAAGCTGCTGCTCAT
CACGAAGAAGAGAGATGACACGTTTACATACAAAGCTCACATCCTGTGTGGCAACCTCATGCTTGTGGAGGTGATTCCAAAAGAGCCGCT
CAGCTTCAGCGTCTTCCACTACAAGAATCCCAAGCTGCAGCACACAGTCCAGGCCAAATCCCAGCAAGACAAACGCCTCTGGGTTCTGCA
CCTAAAGAGACTGATTCTGGAGAACCATGCAGCCAAGATTCCAGCTAAGGCCAAGCAAGCAATCCTTGAAATGGATGCCATTCATCATCC
AGGCTTCTGTTACAGTCCTGAGGGAGGGACGAAAGCACTGTTCGGCTCTAAAGAAGGTTCTGCTCCATATCGGCTGAGAAGAAAATCTGA
AAGATCAACTGAAATCGGCAAACTTCTGAGTTCCTACTTGCAAAAGAAAAGTGACGTGGAGGATCACTCGGTGCACCTGCTTTTTTCTGC
AAATCGCTGGGAACAAGTGCCGTTAATTAAGGAAAAGTTGAGCCAGGGCGTGACCCTCGTCGTGGACAGATACGCATTTTCTGGTGTGGC
CTTCACCGGTGCCAAGGAGAATTTTTCCCTAGATTGGTGTAAACAGCCAGACGTGGGCCTTCCCAAACCCGACCTGGTCCTGTTCCTCCA
GTTACAGCTGGCGGATGCTGCCAAGCGGGGAGCGTTTGGCCATGAGCGCTATGAGAACGGGGCTTTCCAGGAGCGGGCGCTCCGGTGTTT
CCACCAGCTCATGAAAGACACGACTTTGAACTGGAAGATGGTGGATGCTTCCAAAAGCATCGAAGCTGTCCATGAGGACATCCGCGTGCT
CTCTGAGGACGCCATCCGCACTGCCACAGAGAAGCCGCTGGGGGAGCTATGGAAGTGACCCAAGGCTGCCCACTGGAGACGCCTCTCCCT
GCAGTCCCCCGAGAGGTGGGAGACTCGCGGAAGGCCCCGTCCCCAGCAGAGTCCAGACCCCACAACTTCAGGAGCTCTTTCCCGGCAGCA
GAGATCTGCAGGCTGCCTCTTCTGCCCCGGAGCTGGGGTGCACTGGGGACCCCCGTGGTGGGGACCTTGGCAGTGTGGACATGAGCAGAG
CGATGGAGCAGTCTCCTGCCCTCTCCCCTGTCCTGATGGCACTCTGTTGTATTTTCTTACTGAAGTTCAGTGATAACTCTGAGCAGTTTC

>66259_66259_1_PLEKHG1-DTYMK_PLEKHG1_chr6_151140910_ENST00000358517_DTYMK_chr2_242625292_ENST00000305784_length(amino acids)=690AA_BP=521
MRSLHQLKADDVLKPEWSRDGHQLRLEVPSAVTKVPHPKTTARRSCPQELKTMELSDSDRPVSFGSTSSSASSRDSHGSFGSRMTLVSNS
HMGLFNQDKEVGAIKLELIPARPFSSSELQRDNPATGQQNADEGSERPPRAQWRVDSNGAPKTIADSATSPKLLYVDRVVQEILETERTY
VQDLKSIVEDYLDCIRDQTKLPLGTEERSALFGNIQDIYHFNSELLQDLENCENDPVAIAECFVSKSEEFHIYTQYCTNYPRSVAVLTEC
MRNKILAKFFRERQETLKHSLPLGSYLLKPVQRILKYHLLLHEIENHLDKDTEGYDVVLDAIDTMQRVAWHINDMKRKHEHAVRLQEIQS
LLTNWKGPDLTSYGELVLEGTFRIQRAKNERTLFLFDKLLLITKKRDDTFTYKAHILCGNLMLVEVIPKEPLSFSVFHYKNPKLQHTVQA
KSQQDKRLWVLHLKRLILENHAAKIPAKAKQAILEMDAIHHPGFCYSPEGGTKALFGSKEGSAPYRLRRKSERSTEIGKLLSSYLQKKSD
VEDHSVHLLFSANRWEQVPLIKEKLSQGVTLVVDRYAFSGVAFTGAKENFSLDWCKQPDVGLPKPDLVLFLQLQLADAAKRGAFGHERYE

--------------------------------------------------------------
>66259_66259_2_PLEKHG1-DTYMK_PLEKHG1_chr6_151140910_ENST00000367328_DTYMK_chr2_242625292_ENST00000305784_length(transcript)=2614nt_BP=1720nt
GAGGAAGAGGAAGTCGGAGCCCGAGCCTGAGCCCGAGCCCGAGCCCGACGGCGGCTGCAGGGCGCTCCGGCAGCCCGAGCCGGCGCAGCG
CAGCCCGCACCCTCCCCGCCCGACCTGCGAGCGCCGCCCGGGCATGCGAAGCCGTCCCTCCCCGGGTGAAGACTGATGAGAAGAGTCTGT
GGGTGAAGACATTGAAAAGGTTTCAACTATAAAAATGGGCACCAGTTGCGTCTTGAAGTGCCATCAGCTGTAACCAAAGTTCCACATCCC
AAGACGACAGCCAGGCGTTCCTGCCCTCAAGAACTGAAGACAATGGAGCTCTCTGATAGTGACCGACCCGTCAGCTTCGGTTCCACATCA
TCCTCGGCCTCTTCCCGCGACAGCCATGGTTCCTTCGGCAGCAGAATGACCTTAGTTTCAAATAGCCACATGGGCTTGTTTAACCAGGAT
AAGGAGGTAGGGGCCATAAAACTGGAGCTGATTCCTGCCAGGCCGTTTTCCAGCAGCGAGCTGCAGAGGGACAACCCCGCCACGGGGCAA
CAGAACGCGGATGAGGGCAGCGAAAGGCCACCCAGAGCGCAGTGGAGAGTGGACTCAAACGGGGCACCCAAGACGATCGCAGACTCGGCC
ACGAGCCCCAAGCTCCTCTATGTGGATAGAGTTGTTCAGGAAATTCTGGAAACCGAAAGGACTTATGTACAAGATTTAAAAAGCATCGTA
GAGGATTACCTTGACTGCATCAGGGACCAAACAAAACTTCCCCTGGGGACCGAAGAAAGATCAGCCCTTTTTGGAAACATACAGGATATC
TACCACTTCAATAGTGAACTTCTGCAAGATTTGGAAAACTGTGAAAATGATCCTGTGGCCATAGCAGAGTGTTTTGTGTCCAAGAGTGAA
GAGTTCCACATTTATACCCAGTATTGCACTAACTATCCAAGGTCCGTGGCTGTGCTAACAGAGTGTATGAGGAACAAGATACTGGCCAAA
TTCTTCAGGGAGCGTCAGGAAACTCTGAAACACTCGCTGCCTCTGGGGTCCTATCTCTTGAAACCAGTTCAGCGGATTCTCAAGTATCAT
CTCCTTCTGCATGAAATAGAAAACCACCTTGATAAGGACACAGAAGGCTATGATGTGGTGCTTGATGCTATAGACACAATGCAGCGAGTC
GCCTGGCATATCAATGACATGAAGCGGAAACACGAGCACGCGGTCCGGTTACAGGAGATACAGAGTTTGCTCACTAACTGGAAGGGGCCA
GACCTGACCAGCTACGGGGAACTGGTGCTTGAGGGAACCTTCCGCATCCAGCGAGCCAAGAATGAGCGGACGCTCTTCCTCTTCGACAAG
CTGCTGCTCATCACGAAGAAGAGAGATGACACGTTTACATACAAAGCTCACATCCTGTGTGGCAACCTCATGCTTGTGGAGGTGATTCCA
AAAGAGCCGCTCAGCTTCAGCGTCTTCCACTACAAGAATCCCAAGCTGCAGCACACAGTCCAGGCCAAATCCCAGCAAGACAAACGCCTC
TGGGTTCTGCACCTAAAGAGACTGATTCTGGAGAACCATGCAGCCAAGATTCCAGCTAAGGCCAAGCAAGCAATCCTTGAAATGGATGCC
ATTCATCATCCAGGCTTCTGTTACAGTCCTGAGGGAGGGACGAAAGCACTGTTCGGCTCTAAAGAAGGTTCTGCTCCATATCGGCTGAGA
AGAAAATCTGAAAGATCAACTGAAATCGGCAAACTTCTGAGTTCCTACTTGCAAAAGAAAAGTGACGTGGAGGATCACTCGGTGCACCTG
CTTTTTTCTGCAAATCGCTGGGAACAAGTGCCGTTAATTAAGGAAAAGTTGAGCCAGGGCGTGACCCTCGTCGTGGACAGATACGCATTT
TCTGGTGTGGCCTTCACCGGTGCCAAGGAGAATTTTTCCCTAGATTGGTGTAAACAGCCAGACGTGGGCCTTCCCAAACCCGACCTGGTC
CTGTTCCTCCAGTTACAGCTGGCGGATGCTGCCAAGCGGGGAGCGTTTGGCCATGAGCGCTATGAGAACGGGGCTTTCCAGGAGCGGGCG
CTCCGGTGTTTCCACCAGCTCATGAAAGACACGACTTTGAACTGGAAGATGGTGGATGCTTCCAAAAGCATCGAAGCTGTCCATGAGGAC
ATCCGCGTGCTCTCTGAGGACGCCATCCGCACTGCCACAGAGAAGCCGCTGGGGGAGCTATGGAAGTGACCCAAGGCTGCCCACTGGAGA
CGCCTCTCCCTGCAGTCCCCCGAGAGGTGGGAGACTCGCGGAAGGCCCCGTCCCCAGCAGAGTCCAGACCCCACAACTTCAGGAGCTCTT
TCCCGGCAGCAGAGATCTGCAGGCTGCCTCTTCTGCCCCGGAGCTGGGGTGCACTGGGGACCCCCGTGGTGGGGACCTTGGCAGTGTGGA
CATGAGCAGAGCGATGGAGCAGTCTCCTGCCCTCTCCCCTGTCCTGATGGCACTCTGTTGTATTTTCTTACTGAAGTTCAGTGATAACTC
TGAGCAGTTTCATTGTGATCACTGTAAATGGTAATCAGTTGGAATTCTCCTAAATGTCTTCCAGACACTAGTAAAAAACGACCTGAAAAT

>66259_66259_2_PLEKHG1-DTYMK_PLEKHG1_chr6_151140910_ENST00000367328_DTYMK_chr2_242625292_ENST00000305784_length(amino acids)=667AA_BP=498
MRLEVPSAVTKVPHPKTTARRSCPQELKTMELSDSDRPVSFGSTSSSASSRDSHGSFGSRMTLVSNSHMGLFNQDKEVGAIKLELIPARP
FSSSELQRDNPATGQQNADEGSERPPRAQWRVDSNGAPKTIADSATSPKLLYVDRVVQEILETERTYVQDLKSIVEDYLDCIRDQTKLPL
GTEERSALFGNIQDIYHFNSELLQDLENCENDPVAIAECFVSKSEEFHIYTQYCTNYPRSVAVLTECMRNKILAKFFRERQETLKHSLPL
GSYLLKPVQRILKYHLLLHEIENHLDKDTEGYDVVLDAIDTMQRVAWHINDMKRKHEHAVRLQEIQSLLTNWKGPDLTSYGELVLEGTFR
IQRAKNERTLFLFDKLLLITKKRDDTFTYKAHILCGNLMLVEVIPKEPLSFSVFHYKNPKLQHTVQAKSQQDKRLWVLHLKRLILENHAA
KIPAKAKQAILEMDAIHHPGFCYSPEGGTKALFGSKEGSAPYRLRRKSERSTEIGKLLSSYLQKKSDVEDHSVHLLFSANRWEQVPLIKE
KLSQGVTLVVDRYAFSGVAFTGAKENFSLDWCKQPDVGLPKPDLVLFLQLQLADAAKRGAFGHERYENGAFQERALRCFHQLMKDTTLNW

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Fusion Gene PPI Analysis for PLEKHG1-DTYMK


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 PLEKHG1-DTYMK


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 PLEKHG1-DTYMK


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource