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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 13660

FusionGeneSummary for FNBP1_CKB

check button Fusion gene summary
Fusion gene informationFusion gene name: FNBP1_CKB
Fusion gene ID: 13660
HgeneTgene
Gene symbol

FNBP1

CKB

Gene ID

23048

1152

Gene nameformin binding protein 1creatine kinase B
SynonymsFBP17B-CK|BCK|CKBB|CPK-B|HEL-211|HEL-S-29
Cytomap

9q34.11

14q32.33

Type of geneprotein-codingprotein-coding
Descriptionformin-binding protein 1formin-binding protein 17creatine kinase B-typebrain creatine kinasecreatine kinase B chaincreatine kinase braincreatine kinase brain-typecreatine phosphokinase B-typeepididymis luminal protein 211epididymis secretory protein Li 29
Modification date2018052920180519
UniProtAcc

Q96RU3

P12277

Ensembl transtripts involved in fusion geneENST00000446176, ENST00000420781, 
ENST00000355681, ENST00000443566, 
ENST00000478129, 
ENST00000348956, 
Fusion gene scores* DoF score3 X 5 X 1=158 X 11 X 2=176
# samples 1013
** MAII scorelog2(10/15*10)=2.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(13/176*10)=-0.437063805608843
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FNBP1 [Title/Abstract] AND CKB [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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

check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1BE928567FNBP1chr9

132797574

+CKBchr14

103988695

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
intron-3CDSENST00000446176ENST00000348956FNBP1chr9

132797574

+CKBchr14

103988695

+
intron-3CDSENST00000420781ENST00000348956FNBP1chr9

132797574

+CKBchr14

103988695

+
intron-3CDSENST00000355681ENST00000348956FNBP1chr9

132797574

+CKBchr14

103988695

+
intron-3CDSENST00000443566ENST00000348956FNBP1chr9

132797574

+CKBchr14

103988695

+
intron-3CDSENST00000478129ENST00000348956FNBP1chr9

132797574

+CKBchr14

103988695

+

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FusionProtFeatures for FNBP1_CKB


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FNBP1

Q96RU3

CKB

P12277

Reversibly catalyzes the transfer of phosphate betweenATP and various phosphogens (e.g. creatine phosphate). Creatinekinase isoenzymes play a central role in energy transduction intissues with large, fluctuating energy demands, such as skeletalmuscle, heart, brain and spermatozoa.

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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FusionGeneSequence for FNBP1_CKB


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for FNBP1_CKB


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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RelatedDrugs for FNBP1_CKB


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for FNBP1_CKB


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneCKBC0001418Adenocarcinoma1CTD_human
TgeneCKBC0027051Myocardial Infarction1CTD_human
TgeneCKBC0036341Schizophrenia1PSYGENET
TgeneCKBC0038356Stomach Neoplasms1CTD_human
TgeneCKBC0149721Left Ventricular Hypertrophy1CTD_human
TgeneCKBC0149925Small cell carcinoma of lung1CTD_human
TgeneCKBC0857501acute schizophrenia1PSYGENET
TgeneCKBC0948089Acute Coronary Syndrome1CTD_human