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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:CDKL5-SH3KBP1 (FusionGDB2 ID:15417)

Fusion Gene Summary for CDKL5-SH3KBP1

check button Fusion gene summary
Fusion gene informationFusion gene name: CDKL5-SH3KBP1
Fusion gene ID: 15417
HgeneTgene
Gene symbol

CDKL5

SH3KBP1

Gene ID

6792

30011

Gene namecyclin dependent kinase like 5SH3 domain containing kinase binding protein 1
SynonymsCFAP247|EIEE2|ISSX|STK9AGMX2|CD2BP3|CIN85|GIG10|HSB-1|HSB1|IMD61|MIG18
Cytomap

Xp22.13

Xp22.12

Type of geneprotein-codingprotein-coding
Descriptioncyclin-dependent kinase-like 5cyclin dependent kinase 5 transcriptserine/threonine kinase 9serine/threonine-protein kinase 9SH3 domain-containing kinase-binding protein 1CD2-binding protein 3SH3-domain kinase binding protein 1Src family kinase-binding protein 1c-Cbl-interacting proteincbl-interacting protein of 85 kDahuman Src family kinase-binding protein 1migration-in
Modification date2020031520200327
UniProtAcc

O76039

SHKBP1

Ensembl transtripts involved in fusion geneENST00000379996, ENST00000379989, 
ENST00000463994, 
ENST00000397821, 
ENST00000379716, ENST00000379698, 
ENST00000541422, ENST00000379697, 
ENST00000477102, 
Fusion gene scores* DoF score7 X 6 X 3=12615 X 16 X 7=1680
# samples 816
** MAII scorelog2(8/126*10)=-0.655351828612554
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(16/1680*10)=-3.39231742277876
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CDKL5 [Title/Abstract] AND SH3KBP1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCDKL5(18443816)-SH3KBP1(19626164), # samples:1
CDKL5(18528975)-SH3KBP1(19702148), # samples:1
Anticipated loss of major functional domain due to fusion event.CDKL5-SH3KBP1 seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
CDKL5-SH3KBP1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CDKL5-SH3KBP1 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
CDKL5-SH3KBP1 seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneCDKL5

GO:0046777

protein autophosphorylation

16935860

HgeneCDKL5

GO:0099175

regulation of postsynapse organization

22922712


check buttonFusion gene breakpoints across CDKL5 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across SH3KBP1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChiTaRS5.0N/ADA670155CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
ChiTaRS5.0N/ADA672235CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-


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Fusion Gene ORF analysis for CDKL5-SH3KBP1

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5UTR-3CDSENST00000379996ENST00000397821CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
5UTR-3CDSENST00000379996ENST00000379716CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
5UTR-3CDSENST00000379996ENST00000379698CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
5UTR-3CDSENST00000379996ENST00000541422CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
5UTR-3CDSENST00000379996ENST00000379697CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
5UTR-5UTRENST00000379996ENST00000477102CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-3CDSENST00000379989ENST00000397821CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-3CDSENST00000379989ENST00000379716CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-3CDSENST00000379989ENST00000379698CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-3CDSENST00000379989ENST00000541422CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-3CDSENST00000379989ENST00000379697CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-5UTRENST00000379989ENST00000477102CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-3CDSENST00000463994ENST00000397821CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-3CDSENST00000463994ENST00000379716CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-3CDSENST00000463994ENST00000379698CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-3CDSENST00000463994ENST00000541422CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-3CDSENST00000463994ENST00000379697CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
intron-5UTRENST00000463994ENST00000477102CDKL5chrX

18443816

+SH3KBP1chrX

19626164

-
Frame-shiftENST00000379996ENST00000397821CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
5CDS-intronENST00000379996ENST00000379716CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
5CDS-intronENST00000379996ENST00000379698CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
5CDS-intronENST00000379996ENST00000541422CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
5CDS-intronENST00000379996ENST00000379697CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
5CDS-intronENST00000379996ENST00000477102CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
Frame-shiftENST00000379989ENST00000397821CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
5CDS-intronENST00000379989ENST00000379716CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
5CDS-intronENST00000379989ENST00000379698CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
5CDS-intronENST00000379989ENST00000541422CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
5CDS-intronENST00000379989ENST00000379697CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
5CDS-intronENST00000379989ENST00000477102CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
intron-3CDSENST00000463994ENST00000397821CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
intron-intronENST00000463994ENST00000379716CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
intron-intronENST00000463994ENST00000379698CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
intron-intronENST00000463994ENST00000541422CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
intron-intronENST00000463994ENST00000379697CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-
intron-intronENST00000463994ENST00000477102CDKL5chrX

18528975

+SH3KBP1chrX

19702148

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

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

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Fusion Genomic Features for CDKL5-SH3KBP1


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for CDKL5-SH3KBP1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CDKL5

O76039

SH3KBP1

SHKBP1

FUNCTION: Mediates phosphorylation of MECP2 (PubMed:15917271, PubMed:16935860). May regulate ciliogenesis (PubMed:29420175). {ECO:0000269|PubMed:15917271, ECO:0000269|PubMed:16935860, ECO:0000269|PubMed:29420175}.707

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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for CDKL5-SH3KBP1


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for CDKL5-SH3KBP1


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 (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for CDKL5-SH3KBP1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for CDKL5-SH3KBP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCDKL5C1839333EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 223CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneCDKL5C0037769West Syndrome2ORPHANET
HgeneCDKL5C0014544Epilepsy1CTD_human
HgeneCDKL5C0022333Jacksonian Seizure1CTD_human
HgeneCDKL5C0035372Rett Syndrome1CTD_human
HgeneCDKL5C0036572Seizures1CTD_human
HgeneCDKL5C0086237Epilepsy, Cryptogenic1CTD_human
HgeneCDKL5C0149958Complex partial seizures1CTD_human
HgeneCDKL5C0162635Angelman Syndrome1CTD_human;GENOMICS_ENGLAND
HgeneCDKL5C0234533Generalized seizures1CTD_human
HgeneCDKL5C0234535Clonic Seizures1CTD_human
HgeneCDKL5C0236018Aura1CTD_human
HgeneCDKL5C0270824Visual seizure1CTD_human
HgeneCDKL5C0270844Tonic Seizures1CTD_human
HgeneCDKL5C0270846Epileptic drop attack1CTD_human
HgeneCDKL5C0393706Early infantile epileptic encephalopathy with suppression bursts1ORPHANET
HgeneCDKL5C0422850Seizures, Somatosensory1CTD_human
HgeneCDKL5C0422852Seizures, Auditory1CTD_human
HgeneCDKL5C0422853Olfactory seizure1CTD_human
HgeneCDKL5C0422854Gustatory seizure1CTD_human
HgeneCDKL5C0422855Vertiginous seizure1CTD_human
HgeneCDKL5C0494475Tonic - clonic seizures1CTD_human
HgeneCDKL5C0751056Non-epileptic convulsion1CTD_human
HgeneCDKL5C0751110Single Seizure1CTD_human
HgeneCDKL5C0751111Awakening Epilepsy1CTD_human
HgeneCDKL5C0751123Atonic Absence Seizures1CTD_human
HgeneCDKL5C0751494Convulsive Seizures1CTD_human
HgeneCDKL5C0751495Seizures, Focal1CTD_human
HgeneCDKL5C0751496Seizures, Sensory1CTD_human
HgeneCDKL5C1535926Neurodevelopmental Disorders1CTD_human
HgeneCDKL5C2748910Rett Syndrome, Atypical1ORPHANET
HgeneCDKL5C3495874Nonepileptic Seizures1CTD_human
HgeneCDKL5C4048158Convulsions1CTD_human
HgeneCDKL5C4316903Absence Seizures1CTD_human
HgeneCDKL5C4317109Epileptic Seizures1CTD_human
HgeneCDKL5C4317123Myoclonic Seizures1CTD_human
HgeneCDKL5C4505436Generalized Absence Seizures1CTD_human
TgeneSH3KBP1C0007102Malignant tumor of colon1CTD_human
TgeneSH3KBP1C0009375Colonic Neoplasms1CTD_human