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Center for Computational Systems Medicine level2
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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 Structure

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pLDDT scores

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Ramachandran Plot of Fusion Protein Structure

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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:KCMF1-RTN4

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: KCMF1-RTN4
FusionPDB ID: 41327
FusionGDB2.0 ID: 41327
HgeneTgene
Gene symbol

KCMF1

RTN4

Gene ID

56888

57142

Gene namepotassium channel modulatory factor 1reticulon 4
SynonymsDEBT91|FIGC|PCMF|ZZZ1ASY|NI220/250|NOGO|NSP|NSP-CL|Nbla00271|Nbla10545|RTN-X|RTN4-A|RTN4-B1|RTN4-B2|RTN4-C
Cytomap

2p11.2

2p16.1

Type of geneprotein-codingprotein-coding
DescriptionE3 ubiquitin-protein ligase KCMF1FGF-induced in gastric cancerFGF-induced ubiquitin-protein ligase in gastric cancersRING-type E3 ubiquitin transferase KCMF1ZZ-type zinc finger-containing protein 1differentially expressed in branching tubulogenesis 9reticulon-4Human NogoAMy043 proteinfoocenneurite growth inhibitor 220neurite outgrowth inhibitorneuroendocrine-specific protein C homologreticulon 5
Modification date2020031320200327
UniProtAcc

Q9P0J7

.
Ensembl transtripts involved in fusion geneENST idsENST00000409785, ENST00000354474, 
ENST00000402434, ENST00000486085, 
ENST00000317610, ENST00000337526, 
ENST00000357376, ENST00000357732, 
ENST00000394609, ENST00000394611, 
ENST00000404909, ENST00000405240, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score14 X 12 X 7=117627 X 28 X 9=6804
# samples 1835
** MAII scorelog2(18/1176*10)=-2.70781924850669
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(35/6804*10)=-4.28095631383106
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: KCMF1 [Title/Abstract] AND RTN4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)KCMF1(85198590)-RTN4(55214834), # samples:2
Anticipated loss of major functional domain due to fusion event.KCMF1-RTN4 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.
KCMF1-RTN4 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.
KCMF1-RTN4 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.
KCMF1-RTN4 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.
* 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
TgeneRTN4

GO:0030517

negative regulation of axon extension

10667797

TgeneRTN4

GO:0071787

endoplasmic reticulum tubular network formation

24262037|25612671

TgeneRTN4

GO:1905552

positive regulation of protein localization to endoplasmic reticulum

27353365


check buttonFusion gene breakpoints across KCMF1 (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 RTN4 (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
ChimerDB4STADTCGA-D7-8570-01AKCMF1chr2

85198590

+RTN4chr2

55214834

-
ChimerDB4STADTCGA-D7-8570KCMF1chr2

85198590

+RTN4chr2

55214834

-


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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)
ENST00000409785KCMF1chr285198590+ENST00000394609RTN4chr255214834-1908375359940193
ENST00000409785KCMF1chr285198590+ENST00000405240RTN4chr255214834-1908375359940193
ENST00000409785KCMF1chr285198590+ENST00000357376RTN4chr255214834-1908375359940193
ENST00000409785KCMF1chr285198590+ENST00000317610RTN4chr255214834-1908375359940193
ENST00000409785KCMF1chr285198590+ENST00000357732RTN4chr255214834-1908375359940193
ENST00000409785KCMF1chr285198590+ENST00000337526RTN4chr255214834-1908375359940193
ENST00000409785KCMF1chr285198590+ENST00000394611RTN4chr255214834-1908375359940193
ENST00000409785KCMF1chr285198590+ENST00000404909RTN4chr255214834-1908375359940193

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
ENST00000409785ENST00000394609KCMF1chr285198590+RTN4chr255214834-0.0010432230.9989568
ENST00000409785ENST00000405240KCMF1chr285198590+RTN4chr255214834-0.0010432230.9989568
ENST00000409785ENST00000357376KCMF1chr285198590+RTN4chr255214834-0.0010432230.9989568
ENST00000409785ENST00000317610KCMF1chr285198590+RTN4chr255214834-0.0010432230.9989568
ENST00000409785ENST00000357732KCMF1chr285198590+RTN4chr255214834-0.0010432230.9989568
ENST00000409785ENST00000337526KCMF1chr285198590+RTN4chr255214834-0.0010432230.9989568
ENST00000409785ENST00000394611KCMF1chr285198590+RTN4chr255214834-0.0010432230.9989568
ENST00000409785ENST00000404909KCMF1chr285198590+RTN4chr255214834-0.0010432230.9989568

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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

>41327_41327_1_KCMF1-RTN4_KCMF1_chr2_85198590_ENST00000409785_RTN4_chr2_55214834_ENST00000317610_length(amino acids)=193AA_BP=5
MSRHEVVDLLYWRDIKKTGVVFGASLFLLLSLTVFSIVSVTAYIALALLSVTISFRIYKGVIQAIQKSDEGHPFRAYLESEVAISEELVQ
KYSNSALGHVNCTIKELRRLFLVDDLVDSLKFAVLMWVFTYVGALFNGLTLLILALISLFSVPVIYERHQAQIDHYLGLANKNVKDAMAK

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

>41327_41327_2_KCMF1-RTN4_KCMF1_chr2_85198590_ENST00000409785_RTN4_chr2_55214834_ENST00000337526_length(amino acids)=193AA_BP=5
MSRHEVVDLLYWRDIKKTGVVFGASLFLLLSLTVFSIVSVTAYIALALLSVTISFRIYKGVIQAIQKSDEGHPFRAYLESEVAISEELVQ
KYSNSALGHVNCTIKELRRLFLVDDLVDSLKFAVLMWVFTYVGALFNGLTLLILALISLFSVPVIYERHQAQIDHYLGLANKNVKDAMAK

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

>41327_41327_3_KCMF1-RTN4_KCMF1_chr2_85198590_ENST00000409785_RTN4_chr2_55214834_ENST00000357376_length(amino acids)=193AA_BP=5
MSRHEVVDLLYWRDIKKTGVVFGASLFLLLSLTVFSIVSVTAYIALALLSVTISFRIYKGVIQAIQKSDEGHPFRAYLESEVAISEELVQ
KYSNSALGHVNCTIKELRRLFLVDDLVDSLKFAVLMWVFTYVGALFNGLTLLILALISLFSVPVIYERHQAQIDHYLGLANKNVKDAMAK

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

>41327_41327_4_KCMF1-RTN4_KCMF1_chr2_85198590_ENST00000409785_RTN4_chr2_55214834_ENST00000357732_length(amino acids)=193AA_BP=5
MSRHEVVDLLYWRDIKKTGVVFGASLFLLLSLTVFSIVSVTAYIALALLSVTISFRIYKGVIQAIQKSDEGHPFRAYLESEVAISEELVQ
KYSNSALGHVNCTIKELRRLFLVDDLVDSLKFAVLMWVFTYVGALFNGLTLLILALISLFSVPVIYERHQAQIDHYLGLANKNVKDAMAK

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

>41327_41327_5_KCMF1-RTN4_KCMF1_chr2_85198590_ENST00000409785_RTN4_chr2_55214834_ENST00000394609_length(amino acids)=193AA_BP=5
MSRHEVVDLLYWRDIKKTGVVFGASLFLLLSLTVFSIVSVTAYIALALLSVTISFRIYKGVIQAIQKSDEGHPFRAYLESEVAISEELVQ
KYSNSALGHVNCTIKELRRLFLVDDLVDSLKFAVLMWVFTYVGALFNGLTLLILALISLFSVPVIYERHQAQIDHYLGLANKNVKDAMAK

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

>41327_41327_6_KCMF1-RTN4_KCMF1_chr2_85198590_ENST00000409785_RTN4_chr2_55214834_ENST00000394611_length(amino acids)=193AA_BP=5
MSRHEVVDLLYWRDIKKTGVVFGASLFLLLSLTVFSIVSVTAYIALALLSVTISFRIYKGVIQAIQKSDEGHPFRAYLESEVAISEELVQ
KYSNSALGHVNCTIKELRRLFLVDDLVDSLKFAVLMWVFTYVGALFNGLTLLILALISLFSVPVIYERHQAQIDHYLGLANKNVKDAMAK

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

>41327_41327_7_KCMF1-RTN4_KCMF1_chr2_85198590_ENST00000409785_RTN4_chr2_55214834_ENST00000404909_length(amino acids)=193AA_BP=5
MSRHEVVDLLYWRDIKKTGVVFGASLFLLLSLTVFSIVSVTAYIALALLSVTISFRIYKGVIQAIQKSDEGHPFRAYLESEVAISEELVQ
KYSNSALGHVNCTIKELRRLFLVDDLVDSLKFAVLMWVFTYVGALFNGLTLLILALISLFSVPVIYERHQAQIDHYLGLANKNVKDAMAK

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

>41327_41327_8_KCMF1-RTN4_KCMF1_chr2_85198590_ENST00000409785_RTN4_chr2_55214834_ENST00000405240_length(amino acids)=193AA_BP=5
MSRHEVVDLLYWRDIKKTGVVFGASLFLLLSLTVFSIVSVTAYIALALLSVTISFRIYKGVIQAIQKSDEGHPFRAYLESEVAISEELVQ
KYSNSALGHVNCTIKELRRLFLVDDLVDSLKFAVLMWVFTYVGALFNGLTLLILALISLFSVPVIYERHQAQIDHYLGLANKNVKDAMAK

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

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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/chr2:85198590/chr2:55214834)
- 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
KCMF1

Q9P0J7

.
FUNCTION: Has intrinsic E3 ubiquitin ligase activity and promotes ubiquitination. {ECO:0000269|PubMed:15581609}.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.

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
TgeneRTN4chr2:85198590chr2:55214834ENST0000039460907143_14811.333333333333334200.0Compositional biasNote=Poly-Pro
TgeneRTN4chr2:85198590chr2:55214834ENST000003946090730_4711.333333333333334200.0Compositional biasNote=Poly-Glu
TgeneRTN4chr2:85198590chr2:55214834ENST00000317610071005_1192185.33333333333334374.0DomainReticulon
TgeneRTN4chr2:85198590chr2:55214834ENST00000337526291005_11921004.33333333333341193.0DomainReticulon
TgeneRTN4chr2:85198590chr2:55214834ENST00000357376291005_1192798.3333333333334987.0DomainReticulon
TgeneRTN4chr2:85198590chr2:55214834ENST00000357732181005_1192204.33333333333334393.0DomainReticulon
TgeneRTN4chr2:85198590chr2:55214834ENST00000394609071005_119211.333333333333334200.0DomainReticulon
TgeneRTN4chr2:85198590chr2:55214834ENST00000394611291005_1192798.3333333333334987.0DomainReticulon
TgeneRTN4chr2:85198590chr2:55214834ENST00000404909291005_1192798.3333333333334987.0DomainReticulon
TgeneRTN4chr2:85198590chr2:55214834ENST00000405240291005_1192798.3333333333334987.0DomainReticulon
TgeneRTN4chr2:85198590chr2:55214834ENST00000317610071040_1133185.33333333333334374.0Topological domainLumenal
TgeneRTN4chr2:85198590chr2:55214834ENST00000317610071155_1192185.33333333333334374.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000337526291040_11331004.33333333333341193.0Topological domainLumenal
TgeneRTN4chr2:85198590chr2:55214834ENST00000337526291155_11921004.33333333333341193.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000357376291040_1133798.3333333333334987.0Topological domainLumenal
TgeneRTN4chr2:85198590chr2:55214834ENST00000357376291155_1192798.3333333333334987.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000357732181040_1133204.33333333333334393.0Topological domainLumenal
TgeneRTN4chr2:85198590chr2:55214834ENST00000357732181155_1192204.33333333333334393.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000394609071040_113311.333333333333334200.0Topological domainLumenal
TgeneRTN4chr2:85198590chr2:55214834ENST00000394609071155_119211.333333333333334200.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000394611291040_1133798.3333333333334987.0Topological domainLumenal
TgeneRTN4chr2:85198590chr2:55214834ENST00000394611291155_1192798.3333333333334987.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000404909291040_1133798.3333333333334987.0Topological domainLumenal
TgeneRTN4chr2:85198590chr2:55214834ENST00000404909291155_1192798.3333333333334987.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000405240291040_1133798.3333333333334987.0Topological domainLumenal
TgeneRTN4chr2:85198590chr2:55214834ENST00000405240291155_1192798.3333333333334987.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000317610071019_1039185.33333333333334374.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000317610071134_1154185.33333333333334374.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000337526291019_10391004.33333333333341193.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000337526291134_11541004.33333333333341193.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000357376291019_1039798.3333333333334987.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000357376291134_1154798.3333333333334987.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000357732181019_1039204.33333333333334393.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000357732181134_1154204.33333333333334393.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000394609071019_103911.333333333333334200.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000394609071134_115411.333333333333334200.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000394611291019_1039798.3333333333334987.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000394611291134_1154798.3333333333334987.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000404909291019_1039798.3333333333334987.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000404909291134_1154798.3333333333334987.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000405240291019_1039798.3333333333334987.0TransmembraneHelical
TgeneRTN4chr2:85198590chr2:55214834ENST00000405240291134_1154798.3333333333334987.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneKCMF1chr2:85198590chr2:55214834ENST00000409785+17225_2575.333333333333333382.0Coiled coilOntology_term=ECO:0000255
HgeneKCMF1chr2:85198590chr2:55214834ENST00000409785+17333_3365.333333333333333382.0Compositional biasNote=Poly-Ser
HgeneKCMF1chr2:85198590chr2:55214834ENST00000409785+17376_3805.333333333333333382.0Compositional biasNote=Poly-Pro
HgeneKCMF1chr2:85198590chr2:55214834ENST00000409785+173_505.333333333333333382.0Zinc fingerZZ-type
HgeneKCMF1chr2:85198590chr2:55214834ENST00000409785+1778_1015.333333333333333382.0Zinc fingerC2H2-type
TgeneRTN4chr2:85198590chr2:55214834ENST0000031761007143_148185.33333333333334374.0Compositional biasNote=Poly-Pro
TgeneRTN4chr2:85198590chr2:55214834ENST000003176100730_47185.33333333333334374.0Compositional biasNote=Poly-Glu
TgeneRTN4chr2:85198590chr2:55214834ENST0000033752629143_1481004.33333333333341193.0Compositional biasNote=Poly-Pro
TgeneRTN4chr2:85198590chr2:55214834ENST000003375262930_471004.33333333333341193.0Compositional biasNote=Poly-Glu
TgeneRTN4chr2:85198590chr2:55214834ENST0000035737629143_148798.3333333333334987.0Compositional biasNote=Poly-Pro
TgeneRTN4chr2:85198590chr2:55214834ENST000003573762930_47798.3333333333334987.0Compositional biasNote=Poly-Glu
TgeneRTN4chr2:85198590chr2:55214834ENST0000035773218143_148204.33333333333334393.0Compositional biasNote=Poly-Pro
TgeneRTN4chr2:85198590chr2:55214834ENST000003577321830_47204.33333333333334393.0Compositional biasNote=Poly-Glu
TgeneRTN4chr2:85198590chr2:55214834ENST0000039461129143_148798.3333333333334987.0Compositional biasNote=Poly-Pro
TgeneRTN4chr2:85198590chr2:55214834ENST000003946112930_47798.3333333333334987.0Compositional biasNote=Poly-Glu
TgeneRTN4chr2:85198590chr2:55214834ENST0000040490929143_148798.3333333333334987.0Compositional biasNote=Poly-Pro
TgeneRTN4chr2:85198590chr2:55214834ENST000004049092930_47798.3333333333334987.0Compositional biasNote=Poly-Glu
TgeneRTN4chr2:85198590chr2:55214834ENST0000040524029143_148798.3333333333334987.0Compositional biasNote=Poly-Pro
TgeneRTN4chr2:85198590chr2:55214834ENST000004052402930_47798.3333333333334987.0Compositional biasNote=Poly-Glu
TgeneRTN4chr2:85198590chr2:55214834ENST00000317610071_1018185.33333333333334374.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000337526291_10181004.33333333333341193.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000357376291_1018798.3333333333334987.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000357732181_1018204.33333333333334393.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000394609071_101811.333333333333334200.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000394611291_1018798.3333333333334987.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000404909291_1018798.3333333333334987.0Topological domainCytoplasmic
TgeneRTN4chr2:85198590chr2:55214834ENST00000405240291_1018798.3333333333334987.0Topological domainCytoplasmic


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Fusion Protein Structures

check button PDB and CIF files of the predicted fusion proteins
* Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
Fusion protein PDB link (fusion AA seq ID in FusionPDB)HgeneHchrHbpHstrandTgeneTchrTbpTstrandAA seqLen(AA seq)
PDB file >>>241_KCMF1_85198590_RTN4_55214834_ranked_0.pdbKCMF18519859085198590ENST00000404909RTN4chr255214834-
MSRHEVVDLLYWRDIKKTGVVFGASLFLLLSLTVFSIVSVTAYIALALLSVTISFRIYKGVIQAIQKSDEGHPFRAYLESEVAISEELVQ
KYSNSALGHVNCTIKELRRLFLVDDLVDSLKFAVLMWVFTYVGALFNGLTLLILALISLFSVPVIYERHQAQIDHYLGLANKNVKDAMAK
193


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pLDDT score distribution

check button pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
KCMF1_pLDDT.png
all structure
all structure
RTN4_pLDDT.png
all structure
all structure

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
all structure


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Ramachandran Plot of Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.
Fusion AA seq ID in FusionPDB and their Ramachandran plots

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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
KCMF1
RTN4


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 KCMF1-RTN4


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 KCMF1-RTN4


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