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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:KCNN3-LAPTM4B

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: KCNN3-LAPTM4B
FusionPDB ID: 41527
FusionGDB2.0 ID: 41527
HgeneTgene
Gene symbol

KCNN3

LAPTM4B

Gene ID

3782

55353

Gene namepotassium calcium-activated channel subfamily N member 3lysosomal protein transmembrane 4 beta
SynonymsKCa2.3|SK3|SKCA3|ZLS3|hSK3LAPTM4beta|LC27
Cytomap

1q21.3

8q22.1

Type of geneprotein-codingprotein-coding
Descriptionsmall conductance calcium-activated potassium channel protein 3SKCa 3potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3potassium intermediate/small conductance calcium-activated channel, subfamily N, member lysosomal-associated transmembrane protein 4Blysosomal associated protein transmembrane 4 betalysosome-associated transmembrane protein 4-beta
Modification date2020032920200313
UniProtAcc

Q9UGI6

Q86VI4

Ensembl transtripts involved in fusion geneENST idsENST00000358505, ENST00000271915, 
ENST00000361147, ENST00000515643, 
ENST00000445593, ENST00000521545, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score6 X 6 X 5=18014 X 8 X 8=896
# samples 816
** MAII scorelog2(8/180*10)=-1.16992500144231
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/896*10)=-2.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: KCNN3 [Title/Abstract] AND LAPTM4B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)KCNN3(154794565)-LAPTM4B(98817581), # samples:1
Anticipated loss of major functional domain due to fusion event.KCNN3-LAPTM4B 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.
KCNN3-LAPTM4B 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.
KCNN3-LAPTM4B 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.
KCNN3-LAPTM4B 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.
KCNN3-LAPTM4B seems lost the major protein functional domain in Hgene 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
TgeneLAPTM4B

GO:0032509

endosome transport via multivesicular body sorting pathway

25588945

TgeneLAPTM4B

GO:0032911

negative regulation of transforming growth factor beta1 production

26126825


check buttonFusion gene breakpoints across KCNN3 (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 LAPTM4B (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-CG-4449-01AKCNN3chr1

154794565

-LAPTM4Bchr8

98817581

+


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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)
ENST00000271915KCNN3chr1154794565-ENST00000445593LAPTM4Bchr898817581+34661345581926622
ENST00000271915KCNN3chr1154794565-ENST00000521545LAPTM4Bchr898817581+19271345581926623
ENST00000361147KCNN3chr1154794565-ENST00000445593LAPTM4Bchr898817581+2366245131826231
ENST00000361147KCNN3chr1154794565-ENST00000521545LAPTM4Bchr898817581+827245131826232

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
ENST00000271915ENST00000445593KCNN3chr1154794565-LAPTM4Bchr898817581+0.0091465080.9908535
ENST00000271915ENST00000521545KCNN3chr1154794565-LAPTM4Bchr898817581+0.039073870.9609261
ENST00000361147ENST00000445593KCNN3chr1154794565-LAPTM4Bchr898817581+0.0003999520.9996001
ENST00000361147ENST00000521545KCNN3chr1154794565-LAPTM4Bchr898817581+0.0005186490.9994814

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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

>41527_41527_1_KCNN3-LAPTM4B_KCNN3_chr1_154794565_ENST00000271915_LAPTM4B_chr8_98817581_ENST00000445593_length(amino acids)=622AA_BP=428
MREFFHPLFFLQAPLLLSLPAQYNAFLSGSVWTPGSPREPKQAKERTGAKILVGEIGCLAFFEDIFGARVALGWGLVLQGIQPGPKMDTS
GHFHDSGVGDLDEDPKCPCPSSGDEQQQQQQQQQQQQPPPPAPPAAPQQPLGPSLQPQPPQLQQQQQQQQQQQQQQPPHPLSQLAQLQSQ
PVHPGLLHSSPTAFRAPPSSNSTAILHPSSRQGSQLNLNDHLLGHSPSSTATSGPGGGSRHRQASPLVHRRDSNPFTEIAMSSCKYSGGV
MKPLSRLSASRRNLIEAETEGQPLQLFSPSNPPEIVISSREDNHAHQTLLHHPNATHNHQHAGTTASSTTFPKANKRKNQNIGYKLGHRR
ALFEKRKRLSDYALIFGMFGIVVMVIETELSWGLYSKDSMFSLALKCLISLSTIILLGLIIAYHTREVQIINAVVLLILLSALADPDQYN
FSSSELGGDFEFMDDANMCIAIAISLLMILICAMATYGAYKQRAAWIIPFFCYQIFDFALNMLVAITVLIYPNSIQEYIRQLPPNFPYRD

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

>41527_41527_2_KCNN3-LAPTM4B_KCNN3_chr1_154794565_ENST00000271915_LAPTM4B_chr8_98817581_ENST00000521545_length(amino acids)=623AA_BP=428
MREFFHPLFFLQAPLLLSLPAQYNAFLSGSVWTPGSPREPKQAKERTGAKILVGEIGCLAFFEDIFGARVALGWGLVLQGIQPGPKMDTS
GHFHDSGVGDLDEDPKCPCPSSGDEQQQQQQQQQQQQPPPPAPPAAPQQPLGPSLQPQPPQLQQQQQQQQQQQQQQPPHPLSQLAQLQSQ
PVHPGLLHSSPTAFRAPPSSNSTAILHPSSRQGSQLNLNDHLLGHSPSSTATSGPGGGSRHRQASPLVHRRDSNPFTEIAMSSCKYSGGV
MKPLSRLSASRRNLIEAETEGQPLQLFSPSNPPEIVISSREDNHAHQTLLHHPNATHNHQHAGTTASSTTFPKANKRKNQNIGYKLGHRR
ALFEKRKRLSDYALIFGMFGIVVMVIETELSWGLYSKDSMFSLALKCLISLSTIILLGLIIAYHTREVQIINAVVLLILLSALADPDQYN
FSSSELGGDFEFMDDANMCIAIAISLLMILICAMATYGAYKQRAAWIIPFFCYQIFDFALNMLVAITVLIYPNSIQEYIRQLPPNFPYRD

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

>41527_41527_3_KCNN3-LAPTM4B_KCNN3_chr1_154794565_ENST00000361147_LAPTM4B_chr8_98817581_ENST00000445593_length(amino acids)=231AA_BP=37
MERPIKDSMFSLALKCLISLSTIILLGLIIAYHTREVQIINAVVLLILLSALADPDQYNFSSSELGGDFEFMDDANMCIAIAISLLMILI
CAMATYGAYKQRAAWIIPFFCYQIFDFALNMLVAITVLIYPNSIQEYIRQLPPNFPYRDDVMSVNPTCLVLIILLFISIILTFKGYLISC

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

>41527_41527_4_KCNN3-LAPTM4B_KCNN3_chr1_154794565_ENST00000361147_LAPTM4B_chr8_98817581_ENST00000521545_length(amino acids)=232AA_BP=37
MERPIKDSMFSLALKCLISLSTIILLGLIIAYHTREVQIINAVVLLILLSALADPDQYNFSSSELGGDFEFMDDANMCIAIAISLLMILI
CAMATYGAYKQRAAWIIPFFCYQIFDFALNMLVAITVLIYPNSIQEYIRQLPPNFPYRDDVMSVNPTCLVLIILLFISIILTFKGYLISC

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

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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/chr1:154794565/chr8:98817581)
- 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
KCNN3

Q9UGI6

LAPTM4B

Q86VI4

FUNCTION: Forms a voltage-independent potassium channel activated by intracellular calcium (PubMed:31155282). Activation is followed by membrane hyperpolarization. Thought to regulate neuronal excitability by contributing to the slow component of synaptic afterhyperpolarization. The channel is blocked by apamin. {ECO:0000269|PubMed:31155282}.FUNCTION: Required for optimal lysosomal function (PubMed:21224396). Blocks EGF-stimulated EGFR intraluminal sorting and degradation. Conversely by binding with the phosphatidylinositol 4,5-bisphosphate, regulates its PIP5K1C interaction, inhibits HGS ubiquitination and relieves LAPTM4B inhibition of EGFR degradation (PubMed:25588945). Recruits SLC3A2 and SLC7A5 (the Leu transporter) to the lysosome, promoting entry of leucine and other essential amino acid (EAA) into the lysosome, stimulating activation of proton-transporting vacuolar (V)-ATPase protein pump (V-ATPase) and hence mTORC1 activation (PubMed:25998567). Plays a role as negative regulator of TGFB1 production in regulatory T cells (PubMed:26126825). Binds ceramide and facilitates its exit from late endosome in order to control cell death pathways (PubMed:26280656). {ECO:0000269|PubMed:21224396, ECO:0000269|PubMed:25588945, ECO:0000269|PubMed:25998567, ECO:0000269|PubMed:26126825, ECO:0000269|PubMed:26280656}.

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
TgeneLAPTM4Bchr1:154794565chr8:98817581ENST0000044559307163_183124.0318.0TransmembraneHelical
TgeneLAPTM4Bchr1:154794565chr8:98817581ENST0000044559307191_211124.0318.0TransmembraneHelical
TgeneLAPTM4Bchr1:154794565chr8:98817581ENST0000044559307244_264124.0318.0TransmembraneHelical
TgeneLAPTM4Bchr1:154794565chr8:98817581ENST0000052154507117_13733.0227.0TransmembraneHelical
TgeneLAPTM4Bchr1:154794565chr8:98817581ENST0000052154507163_18333.0227.0TransmembraneHelical
TgeneLAPTM4Bchr1:154794565chr8:98817581ENST0000052154507191_21133.0227.0TransmembraneHelical
TgeneLAPTM4Bchr1:154794565chr8:98817581ENST0000052154507244_26433.0227.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-2830_9430.0419.0Compositional biasNote=Gln-rich
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-2842_6430.0419.0Compositional biasNote=Pro-rich
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-28683_68730.0419.0Compositional biasNote=Poly-Gln
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-28727_73030.0419.0Compositional biasNote=Poly-Ser
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-2830_9438.0427.0Compositional biasNote=Gln-rich
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-2842_6438.0427.0Compositional biasNote=Pro-rich
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-28683_68738.0427.0Compositional biasNote=Poly-Gln
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-28727_73038.0427.0Compositional biasNote=Poly-Ser
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-28494_51430.0419.0IntramembranePore-forming%3B Name%3DSegment H5
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-28494_51438.0427.0IntramembranePore-forming%3B Name%3DSegment H5
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-28561_63730.0419.0RegionCalmodulin-binding
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-28561_63738.0427.0RegionCalmodulin-binding
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-28288_30830.0419.0TransmembraneHelical%3B Name%3DSegment S1
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-28315_33530.0419.0TransmembraneHelical%3B Name%3DSegment S2
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-28366_38630.0419.0TransmembraneHelical%3B Name%3DSegment S3
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-28405_42530.0419.0TransmembraneHelical%3B Name%3DSegment S4
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-28454_47430.0419.0TransmembraneHelical%3B Name%3DSegment S5
HgeneKCNN3chr1:154794565chr8:98817581ENST00000358505-28523_54330.0419.0TransmembraneHelical%3B Name%3DSegment S6
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-28288_30838.0427.0TransmembraneHelical%3B Name%3DSegment S1
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-28315_33538.0427.0TransmembraneHelical%3B Name%3DSegment S2
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-28366_38638.0427.0TransmembraneHelical%3B Name%3DSegment S3
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-28405_42538.0427.0TransmembraneHelical%3B Name%3DSegment S4
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-28454_47438.0427.0TransmembraneHelical%3B Name%3DSegment S5
HgeneKCNN3chr1:154794565chr8:98817581ENST00000361147-28523_54338.0427.0TransmembraneHelical%3B Name%3DSegment S6
TgeneLAPTM4Bchr1:154794565chr8:98817581ENST0000044559307117_137124.0318.0TransmembraneHelical


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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
KCNN3
LAPTM4B


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 KCNN3-LAPTM4B


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 KCNN3-LAPTM4B


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