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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:CDK6-LAPTM4B

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CDK6-LAPTM4B
FusionPDB ID: 15294
FusionGDB2.0 ID: 15294
HgeneTgene
Gene symbol

CDK6

LAPTM4B

Gene ID

1021

55353

Gene namecyclin dependent kinase 6lysosomal protein transmembrane 4 beta
SynonymsMCPH12|PLSTIRELAPTM4beta|LC27
Cytomap

7q21.2

8q22.1

Type of geneprotein-codingprotein-coding
Descriptioncyclin-dependent kinase 6cell division protein kinase 6serine/threonine-protein kinase PLSTIRElysosomal-associated transmembrane protein 4Blysosomal associated protein transmembrane 4 betalysosome-associated transmembrane protein 4-beta
Modification date2020032920200313
UniProtAcc

Q00534

Q86VI4

Ensembl transtripts involved in fusion geneENST idsENST00000265734, ENST00000424848, 
ENST00000491250, 
ENST00000445593, 
ENST00000521545, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score12 X 9 X 7=75614 X 8 X 8=896
# samples 1716
** MAII scorelog2(17/756*10)=-2.15285148808337
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: CDK6 [Title/Abstract] AND LAPTM4B [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CDK6(92354939)-LAPTM4B(98817580), # samples:1
Anticipated loss of major functional domain due to fusion event.CDK6-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.
CDK6-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.
CDK6-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.
CDK6-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.
CDK6-LAPTM4B seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
CDK6-LAPTM4B seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
CDK6-LAPTM4B seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
CDK6-LAPTM4B seems lost the major protein functional domain in Hgene 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
HgeneCDK6

GO:0001954

positive regulation of cell-matrix adhesion

10205165

HgeneCDK6

GO:0003323

type B pancreatic cell development

20668294

HgeneCDK6

GO:0006468

protein phosphorylation

8114739

HgeneCDK6

GO:0010468

regulation of gene expression

15254224

HgeneCDK6

GO:0045638

negative regulation of myeloid cell differentiation

17431401

HgeneCDK6

GO:0045656

negative regulation of monocyte differentiation

26542173

HgeneCDK6

GO:0045668

negative regulation of osteoblast differentiation

15254224

HgeneCDK6

GO:0045786

negative regulation of cell cycle

14985467

HgeneCDK6

GO:2000773

negative regulation of cellular senescence

17420273

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 CDK6 (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-RD-A8MVCDK6chr7

92354939

-LAPTM4Bchr8

98817580

+


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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)
ENST00000424848CDK6chr792354939-ENST00000445593LAPTM4Bchr898817580+314210214841602372
ENST00000424848CDK6chr792354939-ENST00000521545LAPTM4Bchr898817580+160310214841602373

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
ENST00000424848ENST00000445593CDK6chr792354939-LAPTM4Bchr898817580+0.0002969460.999703
ENST00000424848ENST00000521545CDK6chr792354939-LAPTM4Bchr898817580+0.0009506060.99904937

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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

>15294_15294_1_CDK6-LAPTM4B_CDK6_chr7_92354939_ENST00000424848_LAPTM4B_chr8_98817580_ENST00000445593_length(amino acids)=372AA_BP=179
MEKDGLCRADQQYECVAEIGEGAYGKVFKARDLKNGGRFVALKRVRVQTGEEGMPLSTIREVAVLRHLETFEHPNVVRLFDVCTVSRTDR
ETKLTLVFEHVDQDLTTYLDKVPEPGVPTETIKDMMFQLLRGLDFLHSHRVVHRDLKPQNILVTSSGQIKLADFGLARIYSFQMALTSVI
INAVVLLILLSALADPDQYNFSSSELGGDFEFMDDANMCIAIAISLLMILICAMATYGAYKQRAAWIIPFFCYQIFDFALNMLVAITVLI
YPNSIQEYIRQLPPNFPYRDDVMSVNPTCLVLIILLFISIILTFKGYLISCVWNCYRYINGRNSSDVLVYVTSNDTTVLLPPYDDATVNG

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>15294_15294_2_CDK6-LAPTM4B_CDK6_chr7_92354939_ENST00000424848_LAPTM4B_chr8_98817580_ENST00000521545_length(amino acids)=373AA_BP=179
MEKDGLCRADQQYECVAEIGEGAYGKVFKARDLKNGGRFVALKRVRVQTGEEGMPLSTIREVAVLRHLETFEHPNVVRLFDVCTVSRTDR
ETKLTLVFEHVDQDLTTYLDKVPEPGVPTETIKDMMFQLLRGLDFLHSHRVVHRDLKPQNILVTSSGQIKLADFGLARIYSFQMALTSVI
INAVVLLILLSALADPDQYNFSSSELGGDFEFMDDANMCIAIAISLLMILICAMATYGAYKQRAAWIIPFFCYQIFDFALNMLVAITVLI
YPNSIQEYIRQLPPNFPYRDDVMSVNPTCLVLIILLFISIILTFKGYLISCVWNCYRYINGRNSSDVLVYVTSNDTTVLLPPYDDATVNG

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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/chr7:92354939/chr8:98817580)
- 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
CDK6

Q00534

LAPTM4B

Q86VI4

FUNCTION: Serine/threonine-protein kinase involved in the control of the cell cycle and differentiation; promotes G1/S transition. Phosphorylates pRB/RB1 and NPM1. Interacts with D-type G1 cyclins during interphase at G1 to form a pRB/RB1 kinase and controls the entrance into the cell cycle. Involved in initiation and maintenance of cell cycle exit during cell differentiation; prevents cell proliferation and regulates negatively cell differentiation, but is required for the proliferation of specific cell types (e.g. erythroid and hematopoietic cells). Essential for cell proliferation within the dentate gyrus of the hippocampus and the subventricular zone of the lateral ventricles. Required during thymocyte development. Promotes the production of newborn neurons, probably by modulating G1 length. Promotes, at least in astrocytes, changes in patterns of gene expression, changes in the actin cytoskeleton including loss of stress fibers, and enhanced motility during cell differentiation. Prevents myeloid differentiation by interfering with RUNX1 and reducing its transcription transactivation activity, but promotes proliferation of normal myeloid progenitors. Delays senescence. Promotes the proliferation of beta-cells in pancreatic islets of Langerhans. May play a role in the centrosome organization during the cell cycle phases (PubMed:23918663). {ECO:0000269|PubMed:12833137, ECO:0000269|PubMed:14985467, ECO:0000269|PubMed:15254224, ECO:0000269|PubMed:15809340, ECO:0000269|PubMed:17420273, ECO:0000269|PubMed:17431401, ECO:0000269|PubMed:20333249, ECO:0000269|PubMed:20668294, ECO:0000269|PubMed:23918663, ECO:0000269|PubMed:8114739}.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
HgeneCDK6chr7:92354939chr8:98817580ENST00000265734-4819_27179.0327.0Nucleotide bindingATP
HgeneCDK6chr7:92354939chr8:98817580ENST00000424848-4819_27179.0327.0Nucleotide bindingATP
TgeneLAPTM4Bchr7:92354939chr8:98817580ENST0000044559307163_183124.0318.0TransmembraneHelical
TgeneLAPTM4Bchr7:92354939chr8:98817580ENST0000044559307191_211124.0318.0TransmembraneHelical
TgeneLAPTM4Bchr7:92354939chr8:98817580ENST0000044559307244_264124.0318.0TransmembraneHelical
TgeneLAPTM4Bchr7:92354939chr8:98817580ENST0000052154507117_13733.0227.0TransmembraneHelical
TgeneLAPTM4Bchr7:92354939chr8:98817580ENST0000052154507163_18333.0227.0TransmembraneHelical
TgeneLAPTM4Bchr7:92354939chr8:98817580ENST0000052154507191_21133.0227.0TransmembraneHelical
TgeneLAPTM4Bchr7:92354939chr8:98817580ENST0000052154507244_26433.0227.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCDK6chr7:92354939chr8:98817580ENST00000265734-4813_300179.0327.0DomainProtein kinase
HgeneCDK6chr7:92354939chr8:98817580ENST00000424848-4813_300179.0327.0DomainProtein kinase
TgeneLAPTM4Bchr7:92354939chr8:98817580ENST0000044559307117_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
CDK6CDKN2C, CDKN2A, CCND1, CDKN2D, PPP2CA, PPM1B, CDK2, CCND2, CCND3, CDKN1B, CDC37, FBXO7, CDKN1A, UHRF2, CDK5R1, ELAVL1, CCNE1, CCNA2, KIF26B, RB1, CDK7, ATXN1, HIST1H1A, PML, HSP90AA1, FOXM1, ZSCAN1, SYNPO2, DEDD2, SRSF12, ZNF101, SNIP1, ZNF335, PRX, EBF4, EIF4ENIF1, RBM23, BCL11A, TCEB3B, PPHLN1, TRA2A, SENP3, NIPBL, CBY1, SSBP2, SIRT1, POGZ, LPIN1, ANKRD12, TPX2, TRAK1, CASC3, CLASRP, PPARGC1A, MSL3, SORBS1, ABI2, N4BP1, VGLL4, TJP2, SRSF11, ZMYM3, ZNF174, SLBP, ZFP36, MZF1, KLF10, TFDP1, ZEB1, SOX5, SOX10, SRSF1, SRSF2, SRSF7, TRA2B, RBL1, RBL2, NUMA1, NFATC3, MYC, MEF2D, MLLT3, ISL1, HSF1, EZH2, FOXO3, ELK1, ATF6B, DDIT3, CDC6, MCM2, MCM10, UCHL1, CDKN2B, WDR33, CDKL3, CDK6, DMBT1, AMY2A, PIGR, CDK4, DAB1, PSMA3, RTFDC1, HSP90AA5P, UBE2W, CCNT2, CCNT1, RCHY1, EIF2AK1, CDKN1C, NTRK1, RUNX1, CTNNB1, AR, VHL, FGFR3, USP17L2, MCF2L2, PAK4, FKBP5, FAM26E, TRIM25, HHV8GK18_gp82, EGLN2, RBPMS, HEXIM1, LARP7, KIAA1429, GBF1, SUMO1, UBE2I, ARNT, BECN1, AKT1, CD44, EPHA2, FGFR4, LATS2, STK11, FZR1, GLIS2, MAP2K3, MAP2K5, NF2, RAF1, RASSF1, ARAF, CBLC, KEAP1, MAP3K5, TEAD2, TERT, TSC1, ERBB2, GLIS1, GRM1, HGF, HIF1A, KAT2A, KDELR2, MAPK14, MET, PDGFRA, TNFRSF1A, TP53, TRIM28, APOBEC1, CCNI, CCNH, OTP, TRIM15, UBE2N, FASN, ACACA, NUPR1, USP51, ATG7, BSPRY, KLC3, CA4, NEU2, METTL21B, PPM1M, FAM96A, EPB41L5, HSP90AB1, PCNA, MAP1LC3B, CALCOCO2,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
CDK6all structure
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 CDK6-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 CDK6-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
HgeneCDK6C0004238Atrial Fibrillation2CTD_human
HgeneCDK6C0025149Medulloblastoma2CTD_human
HgeneCDK6C0205833Medullomyoblastoma2CTD_human
HgeneCDK6C0235480Paroxysmal atrial fibrillation2CTD_human
HgeneCDK6C0278510Childhood Medulloblastoma2CTD_human
HgeneCDK6C0278876Adult Medulloblastoma2CTD_human
HgeneCDK6C0751291Desmoplastic Medulloblastoma2CTD_human
HgeneCDK6C1275668Melanotic medulloblastoma2CTD_human
HgeneCDK6C2585653Persistent atrial fibrillation2CTD_human
HgeneCDK6C3468561familial atrial fibrillation2CTD_human
HgeneCDK6C0002871Anemia1CTD_human
HgeneCDK6C0003873Rheumatoid Arthritis1CTD_human
HgeneCDK6C0004403Autosome Abnormalities1CTD_human
HgeneCDK6C0008625Chromosome Aberrations1CTD_human
HgeneCDK6C0017636Glioblastoma1CTD_human
HgeneCDK6C0023452Childhood Acute Lymphoblastic Leukemia1CTD_human
HgeneCDK6C0023453L2 Acute Lymphoblastic Leukemia1CTD_human
HgeneCDK6C0023467Leukemia, Myelocytic, Acute1CTD_human
HgeneCDK6C0024668Mammary Neoplasms, Experimental1CTD_human
HgeneCDK6C0026998Acute Myeloid Leukemia, M11CTD_human
HgeneCDK6C0038454Cerebrovascular accident1CTD_human
HgeneCDK6C0263454Chloracne1CTD_human
HgeneCDK6C0334588Giant Cell Glioblastoma1CTD_human
HgeneCDK6C0345967Malignant mesothelioma1CTD_human
HgeneCDK6C0677866Brain Stem Neoplasms1CTD_human
HgeneCDK6C0751886Brain Stem Neoplasms, Primary1CTD_human
HgeneCDK6C0751887Medullary Neoplasms1CTD_human
HgeneCDK6C0751888Mesencephalic Neoplasms1CTD_human
HgeneCDK6C0751889Pontine Tumors1CTD_human
HgeneCDK6C0751956Acute Cerebrovascular Accidents1CTD_human
HgeneCDK6C1168401Squamous cell carcinoma of the head and neck1CTD_human
HgeneCDK6C1621958Glioblastoma Multiforme1CTD_human
HgeneCDK6C1879321Acute Myeloid Leukemia (AML-M2)1CTD_human
HgeneCDK6C1961102Precursor Cell Lymphoblastic Leukemia Lymphoma1CTD_human
HgeneCDK6C3711387Autosomal Recessive Primary Microcephaly1ORPHANET
HgeneCDK6C4015156MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE1CTD_human;GENOMICS_ENGLAND;UNIPROT