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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: 16576

FusionGeneSummary for HNRNPF_ZNF569

check button Fusion gene summary
Fusion gene informationFusion gene name: HNRNPF_ZNF569
Fusion gene ID: 16576
HgeneTgene
Gene symbol

HNRNPF

ZNF569

Gene ID

3185

148266

Gene nameheterogeneous nuclear ribonucleoprotein Fzinc finger protein 569
SynonymsHNRPF|OK/SW-cl.23|mcs94-1ZAP1|ZNF
Cytomap

10q11.21

19q13.12

Type of geneprotein-codingprotein-coding
Descriptionheterogeneous nuclear ribonucleoprotein FHnRNP F proteinnucleolin-like protein mcs94-1zinc finger protein 569DNA-binding protein
Modification date2018052220180522
UniProtAcc

P52597

Q5MCW4

Ensembl transtripts involved in fusion geneENST00000443950, ENST00000544000, 
ENST00000357065, ENST00000356053, 
ENST00000337970, ENST00000498176, 
ENST00000392149, ENST00000316950, 
ENST00000392150, ENST00000592490, 
ENST00000589833, ENST00000591073, 
Fusion gene scores* DoF score6 X 5 X 4=1203 X 3 X 3=27
# samples 63
** MAII scorelog2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: HNRNPF [Title/Abstract] AND ZNF569 [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
HgeneHNRNPF

GO:0043484

regulation of RNA splicing

20526337


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
TCGARVOVTCGA-13-0916-01AHNRNPFchr10

43904579

-ZNF569chr19

37956375

-
* 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-intronENST00000443950ENST00000392149HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000443950ENST00000316950HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000443950ENST00000392150HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000443950ENST00000592490HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000443950ENST00000589833HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000443950ENST00000591073HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000544000ENST00000392149HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000544000ENST00000316950HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000544000ENST00000392150HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000544000ENST00000592490HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000544000ENST00000589833HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000544000ENST00000591073HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000357065ENST00000392149HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000357065ENST00000316950HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000357065ENST00000392150HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000357065ENST00000592490HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000357065ENST00000589833HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000357065ENST00000591073HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000356053ENST00000392149HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000356053ENST00000316950HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000356053ENST00000392150HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000356053ENST00000592490HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000356053ENST00000589833HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000356053ENST00000591073HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000337970ENST00000392149HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000337970ENST00000316950HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000337970ENST00000392150HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000337970ENST00000592490HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000337970ENST00000589833HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000337970ENST00000591073HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000498176ENST00000392149HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000498176ENST00000316950HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000498176ENST00000392150HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000498176ENST00000592490HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-intronENST00000498176ENST00000589833HNRNPFchr10

43904579

-ZNF569chr19

37956375

-
intron-5UTRENST00000498176ENST00000591073HNRNPFchr10

43904579

-ZNF569chr19

37956375

-

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FusionProtFeatures for HNRNPF_ZNF569


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

P52597

ZNF569

Q5MCW4

Component of the heterogeneous nuclear ribonucleoprotein(hnRNP) complexes which provide the substrate for the processingevents that pre-mRNAs undergo before becoming functional,translatable mRNAs in the cytoplasm. Plays a role in theregulation of alternative splicing events. Binds G-rich sequencesin pre-mRNAs and keeps target RNA in an unfolded state.{ECO:0000269|PubMed:20526337}. May be involved in transcriptional regulation.{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

- 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 HNRNPF_ZNF569


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 HNRNPF_ZNF569


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
HNRNPFNCBP1, NCBP2, HNRNPH1, TXNL4A, SRRM2, TADA2A, UBC, MYC, HDAC5, ZWINT, PSMA3, NDRG1, VAV2, MBNL1, ELAVL1, ARRB2, SIRT7, HNRNPA1, FBXO25, CUL3, CUL4A, CUL4B, CUL5, CUL2, CDK2, CUL1, COPS5, COPS6, DCUN1D1, CAND1, NEDD8, PRAME, KCND3, RBFOX1, RBMX, HNRNPK, HNRNPR, SRSF1, HNRNPM, SRSF7, U2AF2, HNRNPUL1, DHX9, HNRNPD, DHX15, HNRNPA0, DDX5, HNRNPDL, HSPA5, HNRNPH3, RANBP2, EIF3A, RHOT2, MOGS, NOL11, ZMPSTE24, PLP2, PEX3, RAB21, NDUFAF4, RAB14, RDX, ESR1, MAGOH, EIF4A3, SMURF1, VCAM1, FN1, SNRPC, SF3B4, SF1, RBM4, TOE1, RBFOX2, IQCB1, NOS2, UBL4A, ITGA4, ZNF689, ADRB2, TGM2, CDK8, CLK2, YWHAQ, FBXO6, PARK2, PRPF40A, ACTR3, ABCF3, DHPS, MAP4, DNAAF5, OSGEP, PPME1, PPP1R7, PSMD9, ZPR1, RPA3, RPA2, RPA1, WWOX, ERG, UBASH3B, IVNS1ABP, STAU1, CDC20, CEP250, NEDD1, TP53, FUS, AES, DZIP3, TFG, IKZF3, EIF4ENIF1, CCDC33, C1orf94, HSFY1, CUL7, OBSL1, CCDC8, EED, SUMO2, ILK, IRAK1, HSPB1, FBXW11, NTRK1, BASP1, ALG9, ANKMY2, CCNH, CDK7, CSE1L, EDF1, ELAC2, HARS, HNRNPA1L2, HNRNPA2B1, HNRNPA3, MCM3, NCSTN, PDCD10, TWF1, USP7, PUF60, HNRNPH2, MATR3, GAN, CRY1, MCM2, SNW1, CDC5L, ERBB3, ESRRB, CCDC84, AURKA, CDC73, RNF20, AIRE, WWP2, ZNF746, PECR, HSD17B8, AMMECR1, CDKN2AIP, ANGEL2, RBM7, OBFC1, SUPV3L1, ZCCHC8, ACOX1, SUPT5H, DPP9, CYLD, TRIM25, BRCA1, YAP1ZNF569CBX5, KRT31, KRT40, RHOU, LMNA


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 HNRNPF_ZNF569


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 HNRNPF_ZNF569


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneZNF569C0009404Colorectal Neoplasms1CTD_human