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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: 43144

FusionGeneSummary for ZNF266_MECOM

check button Fusion gene summary
Fusion gene informationFusion gene name: ZNF266_MECOM
Fusion gene ID: 43144
HgeneTgene
Gene symbol

ZNF266

MECOM

Gene ID

10781

2122

Gene namezinc finger protein 266MDS1 and EVI1 complex locus
SynonymsHZF1AML1-EVI-1|EVI1|KMT8E|MDS1|MDS1-EVI1|PRDM3|RUSAT2
Cytomap

19p13.2

3q26.2

Type of geneprotein-codingprotein-coding
Descriptionzinc finger protein 266zinc finger protein 1zinc finger protein HZF1MDS1 and EVI1 complex locus proteinMDS1 and EVI1 complex locus protein EVI1AML1-EVI-1 fusion proteinMDS1 and EVI1 complex locus protein MDS1PR domain 3ecotropic virus integration site 1 protein homologmyelodysplasia syndrome-associated protein 1onc
Modification date2018052320180522
UniProtAcc

Q14584

Q03112

Ensembl transtripts involved in fusion geneENST00000361151, ENST00000361451, 
ENST00000588933, ENST00000588221, 
ENST00000592904, ENST00000590306, 
ENST00000592292, ENST00000588013, 
ENST00000264674, ENST00000392736, 
ENST00000464456, ENST00000472280, 
ENST00000494292, ENST00000468789, 
ENST00000460814, ENST00000433243, 
ENST00000485957, 
Fusion gene scores* DoF score4 X 5 X 3=608 X 7 X 6=336
# samples 410
** MAII scorelog2(4/60*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/336*10)=-1.74846123300404
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZNF266 [Title/Abstract] AND MECOM [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
TgeneMECOM

GO:0045892

negative regulation of transcription, DNA-templated

10856240|11568182

TgeneMECOM

GO:0045893

positive regulation of transcription, DNA-templated

11568182|19767769

TgeneMECOM

GO:0051726

regulation of cell cycle

11568182


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
ChiTaRS3.1BF917110ZNF266chr19

9524224

-MECOMchr3

169326285

+
* 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-intronENST00000361151ENST00000264674ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361151ENST00000392736ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361151ENST00000464456ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361151ENST00000472280ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361151ENST00000494292ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361151ENST00000468789ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361151ENST00000460814ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361151ENST00000433243ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361151ENST00000485957ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361451ENST00000264674ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361451ENST00000392736ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361451ENST00000464456ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361451ENST00000472280ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361451ENST00000494292ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361451ENST00000468789ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361451ENST00000460814ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361451ENST00000433243ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000361451ENST00000485957ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588933ENST00000264674ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588933ENST00000392736ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588933ENST00000464456ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588933ENST00000472280ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588933ENST00000494292ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588933ENST00000468789ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588933ENST00000460814ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588933ENST00000433243ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588933ENST00000485957ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588221ENST00000264674ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588221ENST00000392736ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588221ENST00000464456ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588221ENST00000472280ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588221ENST00000494292ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588221ENST00000468789ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588221ENST00000460814ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588221ENST00000433243ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588221ENST00000485957ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592904ENST00000264674ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592904ENST00000392736ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592904ENST00000464456ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592904ENST00000472280ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592904ENST00000494292ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592904ENST00000468789ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592904ENST00000460814ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592904ENST00000433243ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592904ENST00000485957ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000590306ENST00000264674ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000590306ENST00000392736ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000590306ENST00000464456ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000590306ENST00000472280ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000590306ENST00000494292ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000590306ENST00000468789ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000590306ENST00000460814ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000590306ENST00000433243ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000590306ENST00000485957ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592292ENST00000264674ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592292ENST00000392736ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592292ENST00000464456ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592292ENST00000472280ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592292ENST00000494292ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592292ENST00000468789ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592292ENST00000460814ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592292ENST00000433243ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000592292ENST00000485957ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588013ENST00000264674ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588013ENST00000392736ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588013ENST00000464456ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588013ENST00000472280ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588013ENST00000494292ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588013ENST00000468789ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588013ENST00000460814ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588013ENST00000433243ZNF266chr19

9524224

-MECOMchr3

169326285

+
intron-intronENST00000588013ENST00000485957ZNF266chr19

9524224

-MECOMchr3

169326285

+

Top

FusionProtFeatures for ZNF266_MECOM


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ZNF266

Q14584

MECOM

Q03112

May be involved in transcriptional regulation.

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


Top

FusionGeneSequence for ZNF266_MECOM


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).

Top

FusionGenePPI for ZNF266_MECOM


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


Top

RelatedDrugs for ZNF266_MECOM


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

Top

RelatedDiseases for ZNF266_MECOM


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMECOMC0009375Colonic Neoplasms1CTD_human
TgeneMECOMC0023448Lymphoid leukemia1CTD_human
TgeneMECOMC0023470Myeloid Leukemia1CTD_human
TgeneMECOMC0027439Nasopharyngeal Neoplasms1CTD_human
TgeneMECOMC0919267ovarian neoplasm1CTD_human
TgeneMECOMC1458155Mammary Neoplasms1CTD_human
TgeneMECOMC4225221RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 21UNIPROT