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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: 43659

FusionGeneSummary for ZNF720_SAP30L

check button Fusion gene summary
Fusion gene informationFusion gene name: ZNF720_SAP30L
Fusion gene ID: 43659
HgeneTgene
Gene symbol

ZNF720

SAP30L

Gene ID

124411

79685

Gene namezinc finger protein 720SAP30 like
Synonyms-NS4ATP2
Cytomap

16p11.2

5q33.2

Type of geneprotein-codingprotein-coding
Descriptionputative protein ZNF720histone deacetylase complex subunit SAP30LHCV non-structural protein 4A-transactivated protein 2Sin3A associated protein p30-likesin3 corepressor complex subunit SAP30Lsin3-associated protein p30-like
Modification date2018052220180523
UniProtAcc

Q7Z2F6

Q9HAJ7

Ensembl transtripts involved in fusion geneENST00000539915, ENST00000316491, 
ENST00000531864, ENST00000399681, 
ENST00000398696, ENST00000534369, 
ENST00000297109, ENST00000523198, 
ENST00000440364, ENST00000426761, 
Fusion gene scores* DoF score2 X 2 X 2=82 X 2 X 2=8
# samples 22
** MAII scorelog2(2/8*10)=1.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: ZNF720 [Title/Abstract] AND SAP30L [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
ChiTaRS3.1AW952907ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
* 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
3UTR-intronENST00000539915ENST00000297109ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
3UTR-intronENST00000539915ENST00000523198ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
3UTR-intronENST00000539915ENST00000440364ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
3UTR-intronENST00000539915ENST00000426761ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
3UTR-intronENST00000316491ENST00000297109ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
3UTR-intronENST00000316491ENST00000523198ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
3UTR-intronENST00000316491ENST00000440364ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
3UTR-intronENST00000316491ENST00000426761ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000531864ENST00000297109ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000531864ENST00000523198ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000531864ENST00000440364ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000531864ENST00000426761ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000399681ENST00000297109ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000399681ENST00000523198ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000399681ENST00000440364ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000399681ENST00000426761ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000398696ENST00000297109ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000398696ENST00000523198ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000398696ENST00000440364ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000398696ENST00000426761ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000534369ENST00000297109ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000534369ENST00000523198ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000534369ENST00000440364ZNF720chr16

31770872

+SAP30Lchr5

153830352

+
intron-intronENST00000534369ENST00000426761ZNF720chr16

31770872

+SAP30Lchr5

153830352

+

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FusionProtFeatures for ZNF720_SAP30L


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ZNF720

Q7Z2F6

SAP30L

Q9HAJ7

Isoform 1: Functions as transcription repressor,probably via its interaction with histone deacetylase complexes(PubMed:16820529, PubMed:18070604). Involved in the functionalrecruitment of the class 1 Sin3-histone deacetylase complex (HDAC)to the nucleolus (PubMed:16820529). Binds DNA, apparently withoutsequence-specificity, and bends bound double-stranded DNA(PubMed:19015240). Binds phosphoinositol phosphates(phosphoinositol 3-phosphate, phosphoinositol 4-phosphate andphosphoinositol 5-phosphate) via the same basic sequence motifthat mediates DNA binding and nuclear import (PubMed:19015240,PubMed:26609676). {ECO:0000269|PubMed:16820529,ECO:0000269|PubMed:18070604, ECO:0000269|PubMed:19015240,ECO:0000269|PubMed:26609676}. Isoform 2: Functions as transcription repressor; isoform2 has lower transcription repressor activity than isoform 1 andisoform 3. {ECO:0000269|PubMed:18070604}. Isoform 3: Functions as transcription repressor; itsactivity is marginally lower than that of isoform 1.{ECO:0000269|PubMed:18070604}.

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 ZNF720_SAP30L


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 ZNF720_SAP30L


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 ZNF720_SAP30L


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 ZNF720_SAP30L


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSAP30LC0032460Polycystic Ovary Syndrome1CTD_human