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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:KRT77-VIM

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: KRT77-VIM
FusionPDB ID: 43653
FusionGDB2.0 ID: 43653
HgeneTgene
Gene symbol

KRT77

VIM

Gene ID

374454

7431

Gene namekeratin 77vimentin
SynonymsK1B|KRT1B-
Cytomap

12q13.13

10p13

Type of geneprotein-codingprotein-coding
Descriptionkeratin, type II cytoskeletal 1bCK-1BK77cytokeratin-1Bkeratin 1Bkeratin 77, type IItype-II keratin Kb39vimentinepididymis secretory sperm binding protein
Modification date2020031320200327
UniProtAcc

Q7Z794

VMAC

Ensembl transtripts involved in fusion geneENST idsENST00000341809, ENST00000537195, 
ENST00000485947, ENST00000224237, 
ENST00000544301, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score1 X 1 X 1=142 X 25 X 11=11550
# samples 141
** MAII scorelog2(1/1*10)=3.32192809488736log2(41/11550*10)=-4.81612513168534
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: KRT77 [Title/Abstract] AND VIM [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)KRT77(53086205)-VIM(17277845), # samples:1
Anticipated loss of major functional domain due to fusion event.KRT77-VIM 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.
KRT77-VIM 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.
KRT77-VIM 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.
KRT77-VIM 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.
KRT77-VIM seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
KRT77-VIM 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)

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 KRT77 (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 VIM (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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
ChimerDB4GBMTCGA-27-1830-01AKRT77chr12

53086205

-VIMchr10

17277845

+


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000341809KRT77chr1253086205-ENST00000544301VIMchr1017277845+19421456111627538
ENST00000341809KRT77chr1253086205-ENST00000224237VIMchr1017277845+19501456111627538

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
ENST00000341809ENST00000544301KRT77chr1253086205-VIMchr1017277845+0.0121957930.9878042
ENST00000341809ENST00000224237KRT77chr1253086205-VIMchr1017277845+0.012160280.98783964

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>43653_43653_1_KRT77-VIM_KRT77_chr12_53086205_ENST00000341809_VIM_chr10_17277845_ENST00000224237_length(amino acids)=538AA_BP=176
MDAPANMSHQFSSQSAFSSMSRRVYSTSSSAGSGGGSPAVGSVCYARGRCGGGGYGIHGRGFGSRSLYNLGGSRSISINLMGRSTSGFCQ
GGGVGGFGGGRGFGVGSTGAGGFGGGGFGGAGFGTSNFGLGGFGPYCPPGGIQEVTINQSLLEPLHLEVDPEIQRIKTQEREQIMVLNNK
FASFIDKVRFLEQQNQVLQTKWELLQQVNTSTGTNNLEPLLENYIGDLRRQVDLLSAEQMRQNAEVRSMQDVVEDYKSKYEDEINKRTGS
ENDFVVLKKDVDAAYVSKVDLESRVDTLTGEVNFLKYLFLTELSQVQTHISDTNVILSMDNNRSLDLDSIIDAVRTQYELIAQRSKDEAE
ALYQTKYQELQITAGRHGDDLKNSKMEIAELNRTVQRLQAEISNVKKQIEQMQSLISDAEERGEQALQDAWQKLQDLEEALQQSKEELAR

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

>43653_43653_2_KRT77-VIM_KRT77_chr12_53086205_ENST00000341809_VIM_chr10_17277845_ENST00000544301_length(amino acids)=538AA_BP=176
MDAPANMSHQFSSQSAFSSMSRRVYSTSSSAGSGGGSPAVGSVCYARGRCGGGGYGIHGRGFGSRSLYNLGGSRSISINLMGRSTSGFCQ
GGGVGGFGGGRGFGVGSTGAGGFGGGGFGGAGFGTSNFGLGGFGPYCPPGGIQEVTINQSLLEPLHLEVDPEIQRIKTQEREQIMVLNNK
FASFIDKVRFLEQQNQVLQTKWELLQQVNTSTGTNNLEPLLENYIGDLRRQVDLLSAEQMRQNAEVRSMQDVVEDYKSKYEDEINKRTGS
ENDFVVLKKDVDAAYVSKVDLESRVDTLTGEVNFLKYLFLTELSQVQTHISDTNVILSMDNNRSLDLDSIIDAVRTQYELIAQRSKDEAE
ALYQTKYQELQITAGRHGDDLKNSKMEIAELNRTVQRLQAEISNVKKQIEQMQSLISDAEERGEQALQDAWQKLQDLEEALQQSKEELAR

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

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Fusion Protein Functional Features


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/chr12:53086205/chr10:17277845)
- 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
KRT77

Q7Z794

VIM

VMAC

169

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneKRT77chr12:53086205chr10:17277845ENST00000341809-79164_477475.6666666666667579.0DomainIF rod
HgeneKRT77chr12:53086205chr10:17277845ENST00000341809-79164_200475.6666666666667579.0RegionNote=Coil 1A
HgeneKRT77chr12:53086205chr10:17277845ENST00000341809-791_163475.6666666666667579.0RegionNote=Head
HgeneKRT77chr12:53086205chr10:17277845ENST00000341809-79201_219475.6666666666667579.0RegionNote=Linker 1
HgeneKRT77chr12:53086205chr10:17277845ENST00000341809-79220_311475.6666666666667579.0RegionNote=Coil 1B
HgeneKRT77chr12:53086205chr10:17277845ENST00000341809-79312_335475.6666666666667579.0RegionNote=Linker 12
HgeneKRT77chr12:53086205chr10:17277845ENST00000341809-79336_474475.6666666666667579.0RegionNote=Coil 2
TgeneVIMchr12:53086205chr10:17277845ENST0000022423759408_466409.6666666666667467.0RegionNote=Tail
TgeneVIMchr12:53086205chr10:17277845ENST00000544301610408_466409.6666666666667467.0RegionNote=Tail

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneKRT77chr12:53086205chr10:17277845ENST00000341809-79475_578475.6666666666667579.0RegionNote=Tail
TgeneVIMchr12:53086205chr10:17277845ENST0000022423759154_245409.6666666666667467.0Coiled coilOntology_term=ECO:0000269
TgeneVIMchr12:53086205chr10:17277845ENST0000022423759303_407409.6666666666667467.0Coiled coilOntology_term=ECO:0000269
TgeneVIMchr12:53086205chr10:17277845ENST000002242375996_131409.6666666666667467.0Coiled coilOntology_term=ECO:0000269
TgeneVIMchr12:53086205chr10:17277845ENST00000544301610154_245409.6666666666667467.0Coiled coilOntology_term=ECO:0000269
TgeneVIMchr12:53086205chr10:17277845ENST00000544301610303_407409.6666666666667467.0Coiled coilOntology_term=ECO:0000269
TgeneVIMchr12:53086205chr10:17277845ENST0000054430161096_131409.6666666666667467.0Coiled coilOntology_term=ECO:0000269
TgeneVIMchr12:53086205chr10:17277845ENST0000022423759103_411409.6666666666667467.0DomainIF rod
TgeneVIMchr12:53086205chr10:17277845ENST00000544301610103_411409.6666666666667467.0DomainIF rod
TgeneVIMchr12:53086205chr10:17277845ENST0000022423759326_329409.6666666666667467.0Motif[IL]-x-C-x-x-[DE] motif
TgeneVIMchr12:53086205chr10:17277845ENST00000544301610326_329409.6666666666667467.0Motif[IL]-x-C-x-x-[DE] motif
TgeneVIMchr12:53086205chr10:17277845ENST0000022423759132_153409.6666666666667467.0RegionNote=Linker 1
TgeneVIMchr12:53086205chr10:17277845ENST0000022423759246_268409.6666666666667467.0RegionNote=Linker 12
TgeneVIMchr12:53086205chr10:17277845ENST0000022423759269_407409.6666666666667467.0RegionNote=Coil 2
TgeneVIMchr12:53086205chr10:17277845ENST00000224237592_95409.6666666666667467.0RegionNote=Head
TgeneVIMchr12:53086205chr10:17277845ENST00000544301610132_153409.6666666666667467.0RegionNote=Linker 1
TgeneVIMchr12:53086205chr10:17277845ENST00000544301610246_268409.6666666666667467.0RegionNote=Linker 12
TgeneVIMchr12:53086205chr10:17277845ENST00000544301610269_407409.6666666666667467.0RegionNote=Coil 2
TgeneVIMchr12:53086205chr10:17277845ENST000005443016102_95409.6666666666667467.0RegionNote=Head


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
KRT77
VIM


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to KRT77-VIM


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to KRT77-VIM


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

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