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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: 26946

FusionGeneSummary for PHF21B_NOC4L

check button Fusion gene summary
Fusion gene informationFusion gene name: PHF21B_NOC4L
Fusion gene ID: 26946
HgeneTgene
Gene symbol

PHF21B

NOC4L

Gene ID

112885

79050

Gene namePHD finger protein 21Bnucleolar complex associated 4 homolog
SynonymsBHC80L|PHF4NET49|NOC4|UTP19
Cytomap

22q13.31

12q24.33

Type of geneprotein-codingprotein-coding
DescriptionPHD finger protein 21BPHD finger protein 4nucleolar complex protein 4 homologNOC4 protein homologNOC4-like proteinnucleolar complex-associated protein 4-like protein
Modification date2018051920180523
UniProtAcc

Q96EK2

Q9BVI4

Ensembl transtripts involved in fusion geneENST00000403565, ENST00000313237, 
ENST00000396103, ENST00000404079, 
ENST00000447824, ENST00000462631, 
ENST00000330579, ENST00000535343, 
ENST00000538784, 
Fusion gene scores* DoF score4 X 2 X 4=327 X 2 X 10=140
# samples 412
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(12/140*10)=-0.222392421336448
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PHF21B [Title/Abstract] AND NOC4L [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
TCGARVPRADTCGA-XK-AAJR-01APHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
* 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-3CDSENST00000403565ENST00000330579PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
5UTR-intronENST00000403565ENST00000535343PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
5UTR-5UTRENST00000403565ENST00000538784PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
Frame-shiftENST00000313237ENST00000330579PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
5CDS-intronENST00000313237ENST00000535343PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
5CDS-5UTRENST00000313237ENST00000538784PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
Frame-shiftENST00000396103ENST00000330579PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
5CDS-intronENST00000396103ENST00000535343PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
5CDS-5UTRENST00000396103ENST00000538784PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
Frame-shiftENST00000404079ENST00000330579PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
5CDS-intronENST00000404079ENST00000535343PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
5CDS-5UTRENST00000404079ENST00000538784PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
Frame-shiftENST00000447824ENST00000330579PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
5CDS-intronENST00000447824ENST00000535343PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
5CDS-5UTRENST00000447824ENST00000538784PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
intron-3CDSENST00000462631ENST00000330579PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
intron-intronENST00000462631ENST00000535343PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+
intron-5UTRENST00000462631ENST00000538784PHF21Bchr22

45404426

-NOC4Lchr12

132635526

+

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FusionProtFeatures for PHF21B_NOC4L


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PHF21B

Q96EK2

NOC4L

Q9BVI4


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 PHF21B_NOC4L


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 PHF21B_NOC4L


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
PHF21BHDAC1NOC4LVIM, PLSCR1, DAZAP2, KRT15, SSSCA1, TSC22D4, USHBP1, NECAB2, NT5C2, PRSS23, SIRT7, NOP58, PES1, POLR3C, RPL29, ZNF148, ARL6IP5, SIRT1, CEP250, BHLHE40, DNAJA3, IKZF1, OBSL1, HIST1H1A, STX7, STX12, NIFK, BYSL, PRR11, KRR1, DDX52, DKC1, RPS11, RPS7, IFI16, LCA5, RPGRIP1L, CDC14B, ZNF414, SEC31A, ZNF324B, RPS14, RPL7, GPATCH4, PDGFB, RRS1, SART3, RRP8, HIST1H1T, NCL, FOXA1, URI1


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 PHF21B_NOC4L


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 PHF21B_NOC4L


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