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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:CERK-KIAA1644 (FusionGDB2 ID:15953)

Fusion Gene Summary for CERK-KIAA1644

check button Fusion gene summary
Fusion gene informationFusion gene name: CERK-KIAA1644
Fusion gene ID: 15953
HgeneTgene
Gene symbol

CERK

KIAA1644

Gene ID

64781

85352

Gene nameceramide kinaseshisa like 1
SynonymsLK4|dA59H18.2|dA59H18.3|hCERKKIAA1644
Cytomap

22q13.31

22q13.31

Type of geneprotein-codingprotein-coding
Descriptionceramide kinaseacylsphingosine kinaselipid kinase 4lipid kinase LK4protein shisa-like-1
Modification date2020031320200313
UniProtAcc

Q8TCT0

.
Ensembl transtripts involved in fusion geneENST00000541677, ENST00000216264, 
ENST00000471929, 
ENST00000381176, 
Fusion gene scores* DoF score18 X 11 X 7=13862 X 2 X 1=4
# samples 182
** MAII scorelog2(18/1386*10)=-2.94485844580754
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: CERK [Title/Abstract] AND KIAA1644 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCERK(47115983)-KIAA1644(44645565), # samples:2
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneCERK

GO:0006672

ceramide metabolic process

19501188


check buttonFusion gene breakpoints across CERK (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 KIAA1644 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4SKCMTCGA-DA-A1I7-06ACERKchr22

47115983

-KIAA1644chr22

44645565

-


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Fusion Gene ORF analysis for CERK-KIAA1644

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-3CDSENST00000541677ENST00000381176CERKchr22

47115983

-KIAA1644chr22

44645565

-
In-frameENST00000216264ENST00000381176CERKchr22

47115983

-KIAA1644chr22

44645565

-
intron-3CDSENST00000471929ENST00000381176CERKchr22

47115983

-KIAA1644chr22

44645565

-

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)
ENST00000216264CERKchr2247115983-ENST00000381176KIAA1644chr2244645565-651149229012263212

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
ENST00000216264ENST00000381176CERKchr2247115983-KIAA1644chr2244645565-0.406774880.5932251

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Fusion Genomic Features for CERK-KIAA1644


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.
genomic feature

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 CERK-KIAA1644


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/chr22:47115983/chr22:44645565)
- 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
CERK

Q8TCT0

.
FUNCTION: Catalyzes specifically the phosphorylation of ceramide to form ceramide 1-phosphate (PubMed:11956206, PubMed:16269826, PubMed:19168031). Acts efficiently on natural and analog ceramides (C6, C8, C16 ceramides, and C8-dihydroceramide), to a lesser extent on C2-ceramide and C6-dihydroceramide, but not on other lipids, such as various sphingosines (PubMed:11956206, PubMed:16269826, PubMed:19168031). Shows a greater preference for D-erythro isomer of ceramides (PubMed:16269826). Binds phosphoinositides (PubMed:19168031). {ECO:0000269|PubMed:11956206, ECO:0000269|PubMed:16269826, ECO:0000269|PubMed:19168031}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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
HgeneCERKchr22:47115983chr22:44645565ENST00000216264-3131_115126538.0RegionEssential for enzyme activity
HgeneCERKchr22:47115983chr22:44645565ENST00000216264-3131_125126538.0RegionRequired for binding to sulfatide and phosphoinositides

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCERKchr22:47115983chr22:44645565ENST00000216264-313128_278126538.0DomainDAGKc
HgeneCERKchr22:47115983chr22:44645565ENST00000216264-313138_140126538.0Nucleotide bindingATP
HgeneCERKchr22:47115983chr22:44645565ENST00000216264-313170_174126538.0Nucleotide bindingATP
HgeneCERKchr22:47115983chr22:44645565ENST00000216264-313239_241126538.0Nucleotide bindingATP
HgeneCERKchr22:47115983chr22:44645565ENST00000216264-313502_504126538.0Nucleotide bindingATP
HgeneCERKchr22:47115983chr22:44645565ENST00000216264-313195_198126538.0RegionSubstrate binding
TgeneKIAA1644chr22:47115983chr22:44645565ENST0000038117635119_199199200.0Topological domainCytoplasmic
TgeneKIAA1644chr22:47115983chr22:44645565ENST000003811763526_97199200.0Topological domainExtracellular
TgeneKIAA1644chr22:47115983chr22:44645565ENST000003811763598_118199200.0TransmembraneHelical


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Fusion Gene Sequence for CERK-KIAA1644


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.
>15953_15953_1_CERK-KIAA1644_CERK_chr22_47115983_ENST00000216264_KIAA1644_chr22_44645565_ENST00000381176_length(transcript)=6511nt_BP=492nt
CCGCCTCCCGCCGCCCGCCGCCCGCCGCCCGGGCCACTGCAGGGGCCGCTAACGGTCCGGCGCCCCTCGGCGTCCGCGCGCCCCCAGCCT
GGCGGACGAGCCCGGCGGCGGAGATGGGGGCGACGGGGGCGGCGGAGCCGCTGCAATCCGTGCTGTGGGTGAAGCAGCAGCGCTGCGCCG
TGAGCCTGGAGCCCGCGCGGGCTCTGCTGCGCTGGTGGCGGAGCCCGGGGCCCGGAGCCGGCGCCCCCGGCGCGGATGCCTGCTCTGTGC
CTGTATCTGAGATCATCGCCGTTGAGGAAACAGACGTTCACGGGAAACATCAAGGCAGTGGAAAATGGCAGAAAATGGAAAAGCCTTACG
CTTTTACAGTTCACTGTGTAAAGAGAGCACGACGGCACCGCTGGAAGTGGGCGCAGGTGACTTTCTGGTGTCCAGAGGAGCAGCTGTGTC
ACTTGTGGCTGCAGACCCTGCGGGAGATGCTGGAGAAGCTGAAAAACGCTTTTGCTGTGCCTCAGGATGGGGGAGATGAGATCTGAAGCA
CCCGGTGCAGCCTCCGAGAAGAACAACTTCTACAGAGATGCCAGGGACAGCCGAGGTAGCGGCGGTGGCACAGGAGGAAATGCTGCCTGT
GCCCAAAGCCCCCTTCCGCGGACTTCTAAGATTAGGAGCAAACTCAGGGGTAGGGGCTGGGGGTGCAGGGGAGGGGATTCTGAGCCACCT
GTCCGCAAGCAATAGTCCTATTTTGGGCTGGTGGCTTCTGAGAGGTGACTCATTGTGGACTCAGGATGACCAAGACAAAGCAACTCTGGC
TGATTCCAGCCAGGAGGATTGAGGCCTGTGAGTTATACCTGTGGTTGAAAACCGAAGCTTCCCTTGCCCCTGCTCCCTCCAGTAGTGGCC
CCTTGGGGCTATTTGTGTCAGAATATTGAATGTGCGTGTGTGTGTGCGTGTGTGTGATTTGGGGTGTTCTTTTTGTTTGCTTGGTTGGTT
GGTTTTTATTGGGGCTTCCCCCCTCAAGTTCTCTGATGGGCATGAGTCACCCTCCGGCTGGGGGTTCTCATCCGTGTCAATGTCCGAGCC
GCAAGCTTATTGCTAAGCACAGGGTACGGCCCCTCTGTGTCTCGGGGAGCACTGGGGATTTGAAAATGCCAGTCAGGGTTGTTTCTTACA
GAATTCGTTCCTGTAACAATAGTAATACTAAGGGCTGCATCTCAGGCTGACCACAGGGCAGGTGCCAAGTTAAGTGTTTTCATGCACTCC
CTCTCTCACCACCTGGGAGGCAGGTATGATTAACCCCCTGCAGAAAAACTCACAGTGGGGAAGCGGTGCCGGAACCCAAAGTCCAGGCTC
CAACTCCCTGGACGTGACATGCTCGCCAGCCGGGGTACACCCTGCACAATGCTGGGAGCATCTCCTTGATGCCTCCACCATCACCGCCTG
GAGCGCTGATCCACTCAGCACATTCTGGCTAAGCATCTGCTGTGTGCCAGGCCCCGTGCTGGGCAGTGATGGGAATGAAAGATGAGTTAG
ATCTCATCTCTGCCCCCGGGGAGCCTCCCATCTGGTGGGAGACACAGACACGTGGATCTTTGCTGGAAAGGGTAACAAGGCCATGGAAAC
CCAGGCAGGAGCGTTCTAGAAATCCATCCACTTTCAAGTAGGACTTCCATGCCCGTAACATCCACCCACCGAGCTAATCACCCCCACTCC
TGCCCCGCTGCCCTGGGACACCTATGAGATGGCATCACCTAAATCATCACAAACATCTCCAAAGGCCATGCTGCCAGTGTAGACACACTC
ATTCCATGGGTGTTAGTGATACCAAATCTCCCCCAGCTCTTAGCTCGGGAGGCCCTGCTTGATCAATGTGTGTGTCCTCTGACGCAGTTT
CCTCATTTCATCAGACCTAGTGTTCTCACACTGACCACCCATCCATTCACCAGACACGACAGTGAGCAAGGCAGGTCCCTGCTCACTGTG
CTAGCTTTCTAGCTGGGGCAGGAAGACAGTGAAGAAGGAAGGTGGCGAAGGCAGTGAGTGCTCTGCCGGGAACTCAGTGCCAGGAACTCA
GTTCGAGGGACACGTGAGTGAGACCCTTGTGGACCTGGGGTGGTCTGGGAAGGCCGCCTTGAGCAGATGATTGAAGCCCAGATTTGAATG
ACACACAGGAGCCAGTAATGGGCGTTAAAGATAGGAAAAGAGCATTCCAGGCAGAAGGAACGGCTAGTGCAAAGATCCTGCGGCAGCCAC
AGGCTTGGTGGTTTCAAGGAAGCACAAGAAAGCCAGGTGGCACAAGAAAGCCAGGTGGCTGGGGACCCAGAGGGAAGGCAGAAGGAGATG
AGGGTGATAGTGCCCAGCTCTGGGCTCTGCTGTGAGTCAAGCTGTGCAAACACAATGTCCTGCCTTTGGAAAAGCAGAACAAACTTGCTA
GGGTATAAAGCATCCTCCATTCTGCCTGGCTGTCCATCCTCTCAACAGCCCCATGAAGAAGGGGCTCTCCCCATTTTATGGACAAGAAGA
CAGACTCAGCTGGGTCAAGTGGCTTGCCCAGGATCACACAGGTCAGCTGTGGAAGACCCAGGCCCCTGGCTTCAGTCTTTGGGTCCAGCT
GTCTCCTCCAGGCAGTGCTGCCAGTGTCCAGGCATATGGCTTGGCAAAGTGGGAGAACCTCTGCTTGGGGTCTCGATTGGAGAAAGGAAT
GGCTTCCTCTCCCCTGATGTGAGCCGTCCCAGGGCCATGTTGCCGTAAGGGGGTGCACAGCCTGTCCACTAGCCCAGCTGCGGAAGCCAC
AGCTGTGTCCCACGTGCAGTGCCTCAGAAGGCAGAGGAAGCCTTGAGGTGGGGGCCCAAGACCCAGATTCTGACATCAGCTCTGCCACTG
AGAACAGCGTGACCTCAGGCAAGGTCTGTTACCTCAGTTTCCCCATCGGTAAGAGGAAGGAGTCAGATGGGTATTTAAGGAGTTTGCAAC
CCTCGTGTCCTGCTGTCCTGGACAATGCTCTGTAGGTGCTTCCTCTGCCAAAAAGGAACTGGTGGCCTTGCCTCCCTCTCCTGGACACCT
GGGGTCAAAGGTCACTGCCAAATAGACAGCTAGAACTGGGGTTCACCTAAGCATCCCTTGAGATGTACAACCTTCTAGGAGGACATTCCT
CCTGCCTGCCCCCCTCCCCGCAAGAGGTCTTTTCAGGAATAACTGAAAAACCCATGGGGTTTGTGGTCCTGCTGCTCTGCCAAGTCCCTC
TTGGGCAGCTGGGCTGAGGACTGGAACATTCTGTGGCAAGCAGGAGGCCTCAGCAGAGATCACCAAGACCCAGCACACCTGGTGCAGACA
GCCACGGCATCCTCCTTCCTGCAGGTCACCCCCACGAGCCACTTAACCTCTCAGAGCCTCTGCTTCTCACCTGTCAAGTGTGTGAGGTAG
GGTACCAGTTAGTCACGGTACTTGCTGTCTCACAGAGGAGCCGACAGGTGAGAACAGTGTGCATGTGGGTGTGAACACTCAGTGTGGAAA
GCAGGTGTGTGTGTATTCAATCCCCCAATGGTGTCAAGGGCTCCTCAAAATGCCATGGGTCCCCAGGTCATTGTGATAAACACTGTCCCC
ATCCTGCTGTGGTTGTGGCTGGAAGGTCCCTCAAGGAGTAGACTGTCCCTGAGAACAAGATGGATGCAGGGTAGTGACGAGTTCAAGCAT
AGCTAGAGTTACTGTTTTTTAGCAACTCAACCTGATTTTTTAAGCTGCCTACTTTTACTTTTTACTGTGAGCTTCTGTCCATCACCATGT
AATTTGTAATAATAATAATACAAAAAGAAAAACGAGAGAGAGAAGAGGACAAGATGTCCACAGAGGAATCTGCATTCGAGGCTGTTTGCA
GAACTACCGCGTTTGTAAGGACTGTTTCCCACTGGGAACTGTGTGTAATTAATGAGCAGTTTTATGCTTTCCCTCTCGTCTGTGTACGGT
GTGATTGTTGTGTGTTTCAGAATCTCTATTCAGAACCAATAGCTGGTAATGCCTGCTGGCTCGCTGCCCTCAAGTTAGCCTCTGAACGTG
CCCTGCACCTAGAGAAGCAGCCTTCTCACCCGCCTCACCTGGCTGCTCCAGCGGCCAGGCCAGCCACCTGACCATGACCATTGCTGATGT
GCAACAGGCCTTAATTGAAAAAACACACAAGTACATACATGCACATGCGCGCACACACACAGGTGATTTCACAGGTAGATCTGGTCCCTC
TTGCTGTCTCCAATGCTCTAGAAAGCAGCAAGTAGGCAGCTGACAGTGTTCCCAGGGTGAGTGGCATCTCCCCTCATCATCAGAAAGATT
CAGTCAAATTTTGGCCCAGAGCTGAAGAGGAGGACTTGGGAATGTCAGGGAAAACATGACAGGGCTAGGGGTTAACAGGCTTCTTTGGCC
AGGAGATGGTTTCCAGTTCACCGTCAACCCAAAAGCTCTCTTCAGGTCATGGCAAACAGACCAGGGCTGTGGGTGTGGCTGTGCTTGGCA
CTGACTCCCCCACAGGCCGCTGTCCAGGTTGGCTCAGGATTCCAGCTGCCATCCCCAGGCAGGCCCCTCCGCTGGCTCGGCTGCTTTCAC
AATCACCATGTCTGTCTATTAGAGACTGTGCCATTCAAGGAGACGGGGTCCCCGGGGGTGCAGACTTGTAAAATTTTTTAATTTTTCAAC
TTGGCTGAACTGGTCCCCATCAACAGGAAAAGCCTTCGGAAGTGAATTTACAGATTTCTCCCATGTTTGAAATTAACATAACATGAACCC
AGAAGGCAGAGCTTGCAGTGAGCTGAGATCGCACCAGTGCACTCCAGCCTGGGCAACAGAGTGAGACTCTGTCTAGGTAGGTAGGTAAGA
AGGAAGGAAGGAAGAACAGACCTGGATGGAGTTATTGGGAACATGTCTTATCAATGTTGAAGGGCCCCCTATCACTGTAGGGAGACATCC
ACGTGGGTTGTTTTCGTCTGCTGTGAAAATCTAGGGTTGGAATCATGGAAGCAAACTGCAGGAATTCTTAATCATCCTGCTCACGTGGTG
GGCATCAGAGGGTGTCTGCTTGGCCCCCACAGCACTGGGACAGTCAGAGAGGCCATGAGTGGATGACGCCCTGATCACTGCCCTTTGCAG
TCCAGGAATACCTCACTGGGCTGGGGCCATACCCTGTGCCCTCTGGAAGACAAGCCTGCGCACTTACTATGTGCCAGATGCCATGCACAG
TGCCCTAGTTCCTTGCTGTAGCACCAACACGTCCCACGCTGGTGCTTAAATGCACGCAAACAACTTTGGTGGTTGTGGCCCGAAAAGCTC
AAATGTTAAAGTTAAGCAGTCAGGCAAGCTAGAAGAGGTGAGGAGCCTCCTAGAAAACTCATTCGATGACACGCGCTTCCCTCACCTATT
CAGATACTTGCCGAGTGCCTGCCACTTGCCTGGCCCTGTACCCAGGGCCCATCTGGGAGCCATTCCTGCTATAGCTGGGACCACTTGTGA
AACGGCTAGTTGTGCCTAACAGACATGCTCAGATTCACAAAATGAATTCAGAACACTTACCTGTCCCACCCGTGAAAGTGACCTTGGAGG
TGTCATTGCCCCCCACCACCCCAGTTTCTAGTCCAAGCCAACAGCTGGTGCTAGATAGATGCTTGATGAATGAGCAGATTTGACTGTTAG
TTACTCTGTACCTAAAACTCCTATCTTTACATCAAAGCCCTGACAGATTTGCCCTTGACAGACTGAAATCCGGGGCTGCTGCAGGGTTCA
CCTCCAGGAGGCACCATTCACGACACTGTCCCATAAATGGTAATGGGCTCCCAGGGATACTGTTTACATAGACTGCACTGAGAACGGTGA
CCCTTAGGTTTGTACAATGAGGTACCCTGTTGAATGACCCTAAACCAGCCTCCAAAATGTGCAGGATCCCACATTGGTCAGCGCCAACCC
TGAGCACAGGATCTAAAACTATAGATGATATGGCCACCCTGGCCACAGCTGGAACCAAGCTGGTGGCCCAAGAGAGAGCCTCTTCTTGGA
ATTGCATGTCAGTTTCTCATACGCAGTTTCTTCCTATTTTTCCCATTTCCCGTTTTAAAGCTAGTGGCATACCTCACAGTCAAATAACCA
AGTGGTCAGTGTCTCGACAATGTGCAGTAACGAGGTGGGGGCTGCAAGGGTGAGGGGCTCAGTCACCTTAACAAGGCAGGAGACCTCCCA
CAAAAGGCTGATGTGTCGTCCCCAGGGCCAGCTGGACAAGGGCATGCAGCGCAGGGGTAGGGGGATGGAAATATTTTCTCTCCCGTAAAC
TCTGACTTCATGTGAGCAGGCATGGGGTCTCCCTGAGAGCTGATAACCGGGAAAACCAAAACCAATAATATTCCTAATAATAATACTAGA
ATGTAAGAATAATCATGTGTTTTTCACTGACCGCTGTTGCTCTGCTTTTGTCTTTATATACAGTAGTTTTTATAACAATGTCCCTAGGTT

>15953_15953_1_CERK-KIAA1644_CERK_chr22_47115983_ENST00000216264_KIAA1644_chr22_44645565_ENST00000381176_length(amino acids)=212AA_BP=
MPEVTLFSVAELMSESGSWAPTSRLPLPSEALHVGHSCGFRSWASGQAVHPLTATWPWDGSHQGRGSHSFLQSRPQAEVLPLCQAICLDT
GSTAWRRQLDPKTEARGLGLPQLTCVILGKPLDPAESVFLSIKWGEPLLHGAVERMDSQAEWRMLYTLASLFCFSKGRTLCLHSLTHSRA

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Fusion Gene PPI Analysis for CERK-KIAA1644


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 CERK-KIAA1644


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 CERK-KIAA1644


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource