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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:KCNMB4-ARHGAP9

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: KCNMB4-ARHGAP9
FusionPDB ID: 41507
FusionGDB2.0 ID: 41507
HgeneTgene
Gene symbol

KCNMB4

ARHGAP9

Gene ID

27345

64333

Gene namepotassium calcium-activated channel subfamily M regulatory beta subunit 4Rho GTPase activating protein 9
Synonyms-10C|RGL1
Cytomap

12q15

12q13.3

Type of geneprotein-codingprotein-coding
Descriptioncalcium-activated potassium channel subunit beta-4BK channel beta subunit 4BK channel subunit beta-4BKbeta4MaxiK channel beta-subunit 4big potassium channel beta subunit 4calcium-activated potassium channel, subfamily M subunit beta-4charybdotoxin rho GTPase-activating protein 9rho-type GTPase-activating protein 9
Modification date2020031320200320
UniProtAcc

Q86W47

.
Ensembl transtripts involved in fusion geneENST idsENST00000258111, ENST00000550454, 
ENST00000356411, ENST00000393791, 
ENST00000393797, ENST00000424809, 
ENST00000430041, ENST00000550288, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 4 X 7=3083 X 3 X 3=27
# samples 123
** MAII scorelog2(12/308*10)=-1.35989594508638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: KCNMB4 [Title/Abstract] AND ARHGAP9 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)KCNMB4(70760850)-ARHGAP9(57871052), # samples:3
Anticipated loss of major functional domain due to fusion event.KCNMB4-ARHGAP9 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.
KCNMB4-ARHGAP9 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.
KCNMB4-ARHGAP9 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.
KCNMB4-ARHGAP9 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
HgeneKCNMB4

GO:0001508

action potential

10692449

HgeneKCNMB4

GO:0005513

detection of calcium ion

10692449

HgeneKCNMB4

GO:0006813

potassium ion transport

10692449

HgeneKCNMB4

GO:0019228

neuronal action potential

10692449


check buttonFusion gene breakpoints across KCNMB4 (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 ARHGAP9 (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
ChimerDB4SARCTCGA-DX-AATS-01AKCNMB4chr12

70760850

+ARHGAP9chr12

57871052

-
ChimerDB4SARCTCGA-SG-A6Z7-01AKCNMB4chr12

70760850

+ARHGAP9chr12

57871052

-
ChimerDB4SARCTCGA-SG-A6Z7KCNMB4chr12

70760850

+ARHGAP9chr12

57871052

-


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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)
ENST00000258111KCNMB4chr1270760850+ENST00000393791ARHGAP9chr1257871052-24977951562234692
ENST00000258111KCNMB4chr1270760850+ENST00000356411ARHGAP9chr1257871052-25537951562291711
ENST00000258111KCNMB4chr1270760850+ENST00000424809ARHGAP9chr1257871052-23827951561961601
ENST00000258111KCNMB4chr1270760850+ENST00000393797ARHGAP9chr1257871052-25457951562291711
ENST00000258111KCNMB4chr1270760850+ENST00000550288ARHGAP9chr1257871052-24697951562012618
ENST00000258111KCNMB4chr1270760850+ENST00000430041ARHGAP9chr1257871052-24827951562234692

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
ENST00000258111ENST00000393791KCNMB4chr1270760850+ARHGAP9chr1257871052-0.0392411350.9607589
ENST00000258111ENST00000356411KCNMB4chr1270760850+ARHGAP9chr1257871052-0.038354270.9616457
ENST00000258111ENST00000424809KCNMB4chr1270760850+ARHGAP9chr1257871052-0.049637520.95036244
ENST00000258111ENST00000393797KCNMB4chr1270760850+ARHGAP9chr1257871052-0.037115160.9628848
ENST00000258111ENST00000550288KCNMB4chr1270760850+ARHGAP9chr1257871052-0.0501084030.9498916
ENST00000258111ENST00000430041KCNMB4chr1270760850+ARHGAP9chr1257871052-0.037657080.962343

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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

>41507_41507_1_KCNMB4-ARHGAP9_KCNMB4_chr12_70760850_ENST00000258111_ARHGAP9_chr12_57871052_ENST00000356411_length(amino acids)=711AA_BP=25
MEAGAVRALPAPEGAGGSEAAAAPRGPGGGWGAGGRCRRRRRGRRWPRPLCSRALPLAAHSPAVARRRRWRRRLLPPEAVGLGAGGGRGR
GEHASRREWGAMAKLRVAYEYTEAEDKSIRLGLFLIISGVVSLFIFGFCWLSPALQDLQATEANCTVLSVQQIGEVFECTFTCGADCRGT
SQYPCVQVYVNNSESNSRALLHSDEHQLLTNPKNPGSMEGTQTLKRNNDVLQPQAKGFRSDTGTPEPLDPQGSLSLSQRTSQLDPPALQA
PRPLPQLLDDPHEVEKSGLLNMTKIAQGGRKLRKNWGPSWVVLTGNSLVFYREPPPTAPSSGWGPAGSRPESSVDLRGAALAHGRHLSSR
RNVLHIRTIPGHEFLLQSDHETELRAWHRALRTVIERLVRWVEARREAPTGRDQGSGDRENPLELRLSGSGPAELSAGEDEEEESELVSK
PLLRLSSRRSSIRGPEGTEQNRVRNKLKRLIAKRPPLQSLQERGLLRDQVFGCQLESLCQREGDTVPSFLRLCIAAVDKRGLDVDGIYRV
SGNLAVVQKLRFLVDRERAVTSDGRYVFPEQPGQEGRLDLDSTEWDDIHVVTGALKLFLRELPQPLVPPLLLPHFRAALALSESEQCLSQ

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

>41507_41507_2_KCNMB4-ARHGAP9_KCNMB4_chr12_70760850_ENST00000258111_ARHGAP9_chr12_57871052_ENST00000393791_length(amino acids)=692AA_BP=25
MEAGAVRALPAPEGAGGSEAAAAPRGPGGGWGAGGRCRRRRRGRRWPRPLCSRALPLAAHSPAVARRRRWRRRLLPPEAVGLGAGGGRGR
GEHASRREWGAMAKLRVAYEYTEAEDKSIRLGLFLIISGVVSLFIFGFCWLSPALQDLQATEANCTVLSVQQIGEVFECTFTCGADCRGT
SQYPCVQVYVNNSESNSRALLHSDEHQLLTNPKNPGSMEGTQTLKRNNDVLQPQAKGFRSDTGTPEPLDPQGSLSLSQRTSQLDPPALQA
PRPLPQLLDDPHEVEKSGLLNMTKIAQGGRKLRKNWGPSWVVLTGNSLVFYREPPPTAPSSGWGPAGSRPESSVDLRGAALAHGRHLSSR
RNVLHIRTIPGHEFLLQSDHETELRAWHRALRTVIERLDRENPLELRLSGSGPAELSAGEDEEEESELVSKPLLRLSSRRSSIRGPEGTE
QNRVRNKLKRLIAKRPPLQSLQERGLLRDQVFGCQLESLCQREGDTVPSFLRLCIAAVDKRGLDVDGIYRVSGNLAVVQKLRFLVDRERA
VTSDGRYVFPEQPGQEGRLDLDSTEWDDIHVVTGALKLFLRELPQPLVPPLLLPHFRAALALSESEQCLSQIQELIGSMPKPNHDTLRYL

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

>41507_41507_3_KCNMB4-ARHGAP9_KCNMB4_chr12_70760850_ENST00000258111_ARHGAP9_chr12_57871052_ENST00000393797_length(amino acids)=711AA_BP=25
MEAGAVRALPAPEGAGGSEAAAAPRGPGGGWGAGGRCRRRRRGRRWPRPLCSRALPLAAHSPAVARRRRWRRRLLPPEAVGLGAGGGRGR
GEHASRREWGAMAKLRVAYEYTEAEDKSIRLGLFLIISGVVSLFIFGFCWLSPALQDLQATEANCTVLSVQQIGEVFECTFTCGADCRGT
SQYPCVQVYVNNSESNSRALLHSDEHQLLTNPKNPGSMEGTQTLKRNNDVLQPQAKGFRSDTGTPEPLDPQGSLSLSQRTSQLDPPALQA
PRPLPQLLDDPHEVEKSGLLNMTKIAQGGRKLRKNWGPSWVVLTGNSLVFYREPPPTAPSSGWGPAGSRPESSVDLRGAALAHGRHLSSR
RNVLHIRTIPGHEFLLQSDHETELRAWHRALRTVIERLVRWVEARREAPTGRDQGSGDRENPLELRLSGSGPAELSAGEDEEEESELVSK
PLLRLSSRRSSIRGPEGTEQNRVRNKLKRLIAKRPPLQSLQERGLLRDQVFGCQLESLCQREGDTVPSFLRLCIAAVDKRGLDVDGIYRV
SGNLAVVQKLRFLVDRERAVTSDGRYVFPEQPGQEGRLDLDSTEWDDIHVVTGALKLFLRELPQPLVPPLLLPHFRAALALSESEQCLSQ

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

>41507_41507_4_KCNMB4-ARHGAP9_KCNMB4_chr12_70760850_ENST00000258111_ARHGAP9_chr12_57871052_ENST00000424809_length(amino acids)=601AA_BP=25
MEAGAVRALPAPEGAGGSEAAAAPRGPGGGWGAGGRCRRRRRGRRWPRPLCSRALPLAAHSPAVARRRRWRRRLLPPEAVGLGAGGGRGR
GEHASRREWGAMAKLRVAYEYTEAEDKSIRLGLFLIISGVVSLFIFGFCWLSPALQDLQATEANCTVLSVQQIGEVFECTFTCGADCRGT
SQYPCVQVYVNNSESNSRALLHSDEHQLLTNPKNPGSMEGTQTLKRNNDVLQPQAKGFRSDTGTPEPLDPQGSLSLSQRTSQLDPPALQA
PRPLPQLLDDPHEVEKSGLLNMTKIAQGGRKLRKNWGPSWVVLTGNSLVFYREPPPTAPSSGWGPAGSRPESSVDLRGAALAHGRHLSSR
RNVLHIRTIPGHEFLLQSDHETELRAWHRALRTVIERLDRENPLELRLSGSGPAELSAGEDEEEESELVSKPLLRLSSRRSSIRGPEGTE
QNRVRNKLKRLIAKRPPLQSLQERGLLRDQVFGCQLESLCQREGDTVPSFLRLCIAAVDKRGLDVDGIYRVSGNLAVVQKLRFLVDRERA

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

>41507_41507_5_KCNMB4-ARHGAP9_KCNMB4_chr12_70760850_ENST00000258111_ARHGAP9_chr12_57871052_ENST00000430041_length(amino acids)=692AA_BP=25
MEAGAVRALPAPEGAGGSEAAAAPRGPGGGWGAGGRCRRRRRGRRWPRPLCSRALPLAAHSPAVARRRRWRRRLLPPEAVGLGAGGGRGR
GEHASRREWGAMAKLRVAYEYTEAEDKSIRLGLFLIISGVVSLFIFGFCWLSPALQDLQATEANCTVLSVQQIGEVFECTFTCGADCRGT
SQYPCVQVYVNNSESNSRALLHSDEHQLLTNPKNPGSMEGTQTLKRNNDVLQPQAKGFRSDTGTPEPLDPQGSLSLSQRTSQLDPPALQA
PRPLPQLLDDPHEVEKSGLLNMTKIAQGGRKLRKNWGPSWVVLTGNSLVFYREPPPTAPSSGWGPAGSRPESSVDLRGAALAHGRHLSSR
RNVLHIRTIPGHEFLLQSDHETELRAWHRALRTVIERLDRENPLELRLSGSGPAELSAGEDEEEESELVSKPLLRLSSRRSSIRGPEGTE
QNRVRNKLKRLIAKRPPLQSLQERGLLRDQVFGCQLESLCQREGDTVPSFLRLCIAAVDKRGLDVDGIYRVSGNLAVVQKLRFLVDRERA
VTSDGRYVFPEQPGQEGRLDLDSTEWDDIHVVTGALKLFLRELPQPLVPPLLLPHFRAALALSESEQCLSQIQELIGSMPKPNHDTLRYL

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

>41507_41507_6_KCNMB4-ARHGAP9_KCNMB4_chr12_70760850_ENST00000258111_ARHGAP9_chr12_57871052_ENST00000550288_length(amino acids)=618AA_BP=25
MEAGAVRALPAPEGAGGSEAAAAPRGPGGGWGAGGRCRRRRRGRRWPRPLCSRALPLAAHSPAVARRRRWRRRLLPPEAVGLGAGGGRGR
GEHASRREWGAMAKLRVAYEYTEAEDKSIRLGLFLIISGVVSLFIFGFCWLSPALQDLQATEANCTVLSVQQIGEVFECTFTCGADCRGT
SQYPCVQVYVNNSESNSRALLHSDEHQLLTNPKNPGSMEGTQTLKRNNDVLQPQAKGFRSDTGTPEPLDPQGSLSLSQRTSQLDPPALQA
PRPLPQLLDDPHEVEKSGLLNMTKIAQGGRKLRKNWGPSWVVLTGNSLVFYREPPPTAPSSGWGPAGSRPESSVDLRGAALAHGRHLSSR
RNVLHIRTIPGHEFLLQSDHETELRAWHRALRTVIERLDRENPLELRLSGSGPAELSAGEDEEEESELVSKPLLRLSSRRSSIRGPEGTE
QNRVRNKLKRLIAKRPPLQSLQERGLLRDQVFGCQLESLCQREGDTVPSFLRLCIAAVDKRGLDVDGIYRVSGNLAVVQKLRFLVDRERA

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

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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/chr12:70760850/chr12:57871052)
- 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
KCNMB4

Q86W47

.
FUNCTION: Regulatory subunit of the calcium activated potassium KCNMA1 (maxiK) channel. Modulates the calcium sensitivity and gating kinetics of KCNMA1, thereby contributing to KCNMA1 channel diversity. Decreases the gating kinetics and calcium sensitivity of the KCNMA1 channel, but with fast deactivation kinetics. May decrease KCNMA1 channel openings at low calcium concentrations but increases channel openings at high calcium concentrations. Makes KCNMA1 channel resistant to 100 nM charybdotoxin (CTX) toxin concentrations. {ECO:0000269|PubMed:10692449, ECO:0000269|PubMed:10792058, ECO:0000269|PubMed:10828459}.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
HgeneKCNMB4chr12:70760850chr12:57871052ENST00000258111+131_19112.0211.0Topological domainCytoplasmic
HgeneKCNMB4chr12:70760850chr12:57871052ENST00000258111+1320_40112.0211.0TransmembraneHelical%3B Name%3D1
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000356411318322_435252.0751.0DomainPH
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000356411318542_749252.0751.0DomainRho-GAP
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000393791318322_435252.0732.0DomainPH
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000393791318542_749252.0732.0DomainRho-GAP
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000424809216322_435252.0641.0DomainPH
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000424809216542_749252.0641.0DomainRho-GAP
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000430041116213_24768.0548.0DomainWW
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000430041116322_43568.0548.0DomainPH
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000430041116542_74968.0548.0DomainRho-GAP
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000356411318342_345252.0751.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000356411318397_399252.0751.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000356411318432_669252.0751.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000393791318342_345252.0732.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000393791318397_399252.0732.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000393791318432_669252.0732.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000424809216342_345252.0641.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000424809216397_399252.0641.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000424809216432_669252.0641.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000430041116342_34568.0548.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000430041116397_39968.0548.0RegionNote=Lipid binding
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000430041116432_66968.0548.0RegionNote=Lipid binding

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneKCNMB4chr12:70760850chr12:57871052ENST00000258111+13189_210112.0211.0Topological domainCytoplasmic
HgeneKCNMB4chr12:70760850chr12:57871052ENST00000258111+1341_167112.0211.0Topological domainExtracellular
HgeneKCNMB4chr12:70760850chr12:57871052ENST00000258111+13168_188112.0211.0TransmembraneHelical%3B Name%3D2
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000356411318213_247252.0751.0DomainWW
TgeneARHGAP9chr12:70760850chr12:57871052ENST0000035641131822_88252.0751.0DomainSH3
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000393791318213_247252.0732.0DomainWW
TgeneARHGAP9chr12:70760850chr12:57871052ENST0000039379131822_88252.0732.0DomainSH3
TgeneARHGAP9chr12:70760850chr12:57871052ENST00000424809216213_247252.0641.0DomainWW
TgeneARHGAP9chr12:70760850chr12:57871052ENST0000042480921622_88252.0641.0DomainSH3
TgeneARHGAP9chr12:70760850chr12:57871052ENST0000043004111622_8868.0548.0DomainSH3


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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 >>>1452_KCNMB4_70760850_ARHGAP9_57871052_ranked_0.pdbKCNMB47076085070760850ENST00000430041ARHGAP9chr1257871052-
MEAGAVRALPAPEGAGGSEAAAAPRGPGGGWGAGGRCRRRRRGRRWPRPLCSRALPLAAHSPAVARRRRWRRRLLPPEAVGLGAGGGRGR
GEHASRREWGAMAKLRVAYEYTEAEDKSIRLGLFLIISGVVSLFIFGFCWLSPALQDLQATEANCTVLSVQQIGEVFECTFTCGADCRGT
SQYPCVQVYVNNSESNSRALLHSDEHQLLTNPKNPGSMEGTQTLKRNNDVLQPQAKGFRSDTGTPEPLDPQGSLSLSQRTSQLDPPALQA
PRPLPQLLDDPHEVEKSGLLNMTKIAQGGRKLRKNWGPSWVVLTGNSLVFYREPPPTAPSSGWGPAGSRPESSVDLRGAALAHGRHLSSR
RNVLHIRTIPGHEFLLQSDHETELRAWHRALRTVIERLVRWVEARREAPTGRDQGSGDRENPLELRLSGSGPAELSAGEDEEEESELVSK
PLLRLSSRRSSIRGPEGTEQNRVRNKLKRLIAKRPPLQSLQERGLLRDQVFGCQLESLCQREGDTVPSFLRLCIAAVDKRGLDVDGIYRV
SGNLAVVQKLRFLVDRERAVTSDGRYVFPEQPGQEGRLDLDSTEWDDIHVVTGALKLFLRELPQPLVPPLLLPHFRAALALSESEQCLSQ
711


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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.
KCNMB4_pLDDT.png
all structure
all structure
ARHGAP9_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
KCNMB4
ARHGAP9


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 KCNMB4-ARHGAP9


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 KCNMB4-ARHGAP9


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