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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: 8189

FusionGeneSummary for COX7B2_PIP4K2A

check button Fusion gene summary
Fusion gene informationFusion gene name: COX7B2_PIP4K2A
Fusion gene ID: 8189
HgeneTgene
Gene symbol

COX7B2

PIP4K2A

Gene ID

170712

5305

Gene namecytochrome c oxidase subunit 7B2phosphatidylinositol-5-phosphate 4-kinase type 2 alpha
Synonyms-PI5P4KA|PIP5K2A|PIP5KII-alpha|PIP5KIIA|PIPK
Cytomap

4p12

10p12.2

Type of geneprotein-codingprotein-coding
Descriptioncytochrome c oxidase subunit 7B2, mitochondrialcytochrome c oxidase polypeptide VIIb2cytochrome c oxidase subunit VIIb2phosphatidylinositol 5-phosphate 4-kinase type-2 alpha1-phosphatidylinositol 5-phosphate 4-kinase 2-alpha1-phosphatidylinositol-4-phosphate kinase1-phosphatidylinositol-4-phosphate-5-kinasePI(5)P 4-kinase type II alphaPIP4KII-alphaPIP5KIIIPIP5KIIal
Modification date2018032920180522
UniProtAcc

Q8TF08

P48426

Ensembl transtripts involved in fusion geneENST00000396533, ENST00000355591, 
ENST00000543208, ENST00000302930, 
ENST00000376573, ENST00000545335, 
ENST00000323883, ENST00000422321, 
Fusion gene scores* DoF score1 X 1 X 1=14 X 2 X 4=32
# samples 14
** MAII scorelog2(1/1*10)=3.32192809488736log2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: COX7B2 [Title/Abstract] AND PIP4K2A [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
TCGARVLUSCTCGA-NC-A5HM-01ACOX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
* 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
5UTR-3CDSENST00000396533ENST00000376573COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
5UTR-5UTRENST00000396533ENST00000545335COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
5UTR-intronENST00000396533ENST00000323883COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
5UTR-intronENST00000396533ENST00000422321COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
5UTR-3CDSENST00000355591ENST00000376573COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
5UTR-5UTRENST00000355591ENST00000545335COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
5UTR-intronENST00000355591ENST00000323883COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
5UTR-intronENST00000355591ENST00000422321COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
intron-3CDSENST00000543208ENST00000376573COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
intron-5UTRENST00000543208ENST00000545335COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
intron-intronENST00000543208ENST00000323883COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
intron-intronENST00000543208ENST00000422321COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
intron-3CDSENST00000302930ENST00000376573COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
intron-5UTRENST00000302930ENST00000545335COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
intron-intronENST00000302930ENST00000323883COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-
intron-intronENST00000302930ENST00000422321COX7B2chr4

46911177

-PIP4K2Achr10

22898646

-

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FusionProtFeatures for COX7B2_PIP4K2A


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
COX7B2

Q8TF08

PIP4K2A

P48426

This protein is one of the nuclear-coded polypeptidechains of cytochrome c oxidase, the terminal oxidase inmitochondrial electron transport. Catalyzes the phosphorylation of phosphatidylinositol 5-phosphate (PtdIns5P) on the fourth hydroxyl of the myo-inositolring, to form phosphatidylinositol 4,5-bisphosphate(PtdIns(4,5)P2). May exert its function by regulating the levelsof PtdIns5P, which functions in the cytosol by increasing AKTactivity and in the nucleus signals through ING2. May regulate thepool of cytosolic PtdIns5P in response to the activation oftyrosine phosphorylation. May negatively regulate insulin-stimulated glucose uptake by lowering the levels of PtdIns5P. Maybe involved in thrombopoiesis, and the terminal maturation ofmegakaryocytes and regulation of their size.{ECO:0000269|PubMed:18364242}.

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 COX7B2_PIP4K2A


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 COX7B2_PIP4K2A


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
COX7B2PIP4K2AGRK5, GSTK1, CSNK2A2, ARL6IP4, EAF1, ZRANB2, EPB41L3, CSNK2A1, CSNK2B, DDX23, MTPN, PRPF8, SKP1, KRAS, IFI16, MED4, RPS6KB1, PIP4K2B, DIP2C, UBTF, AFF3, RTF1, AFF4, HDGFRP2, BRD3, MLLT3, PIP4K2C, PNISR, MEX3B, STRADA, MLLT1, AFF1, ELL3, BRD2, GPATCH8, CHD9, AHCYL2, STK11, BRD4, NAF1, GPALPP1, MEX3C, PIP5K1A, EAF2, BRPF1, GPBP1L1, ACIN1, SETD1B, RNPS1, ELL2, AHCYL1, KANK1, CWC22, LENG8, RAD18, PPRC1, STRADB, C12orf43, DNAJC13, PLCD3, NFKBIL1, CAB39, AP3B1, NOLC1, PNN, RFWD3, ELL, CLASRP, PPIG, JMJD6, CXXC1, SBF1, LZTS2, CCNT1, GTF2F1, IWS1, EDC4, SRSF8, C11orf31, ARHGAP22, TCOF1, SRRM2, CCDC102A, WDR26, AP3M1, C18orf25, PRICKLE3, SETD2, SPEN, TMEM194A, NOS1AP, MTMR1, CHD8, EPB41L5, PIN1, ST6GAL1, NKAP, CCDC9, RAB11FIP1, ZNF428, SUN2


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 COX7B2_PIP4K2A


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 COX7B2_PIP4K2A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePIP4K2AC0036341Schizophrenia4PSYGENET
TgenePIP4K2AC0005586Bipolar Disorder3PSYGENET
TgenePIP4K2AC0025202melanoma1CTD_human