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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:CCSER2-HINFP (FusionGDB2 ID:14268)

Fusion Gene Summary for CCSER2-HINFP

check button Fusion gene summary
Fusion gene informationFusion gene name: CCSER2-HINFP
Fusion gene ID: 14268
HgeneTgene
Gene symbol

CCSER2

HINFP

Gene ID

54462

25988

Gene namecoiled-coil serine rich protein 2histone H4 transcription factor
SynonymsFAM190B|Gcap14|KIAA1128|bA486O22.1HiNF-P|MIZF|ZNF743
Cytomap

10q23.1

11q23.3

Type of geneprotein-codingprotein-coding
Descriptionserine-rich coiled-coil domain-containing protein 2family with sequence similarity 190, member Bprotein FAM190Bprotein GCAP14 homologhistone H4 transcription factorMBD2 (methyl-CpG-binding protein)-interacting zinc finger proteinMBD2-interacting zinc finger 1MBD2-interacting zinc finger proteinhistone H4 gene-specific protein HiNF-Phistone nuclear factor Pmethyl-CpG-binding prote
Modification date2020031320200313
UniProtAcc

Q9H7U1

Q9BQA5

Ensembl transtripts involved in fusion geneENST00000224756, ENST00000359979, 
ENST00000372088, ENST00000494144, 
ENST00000543283, 
ENST00000350777, 
ENST00000527354, ENST00000527410, 
Fusion gene scores* DoF score7 X 7 X 4=1962 X 2 X 1=4
# samples 82
** MAII scorelog2(8/196*10)=-1.29278174922785
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: CCSER2 [Title/Abstract] AND HINFP [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCCSER2(86154692)-HINFP(119005747), # samples:1
Anticipated loss of major functional domain due to fusion event.
* 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
TgeneHINFP

GO:0045892

negative regulation of transcription, DNA-templated

11553631|14752047|15541338|17163457

TgeneHINFP

GO:0045893

positive regulation of transcription, DNA-templated

14585971|17163457|17974976


check buttonFusion gene breakpoints across CCSER2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across HINFP (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ADN916609CCSER2chr10

86154692

+HINFPchr11

119005747

-


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Fusion Gene ORF analysis for CCSER2-HINFP

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-3UTRENST00000224756ENST00000350777CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-3UTRENST00000359979ENST00000350777CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-3UTRENST00000372088ENST00000350777CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-3UTRENST00000494144ENST00000350777CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-3UTRENST00000543283ENST00000350777CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-intronENST00000224756ENST00000527354CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-intronENST00000224756ENST00000527410CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-intronENST00000359979ENST00000527354CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-intronENST00000359979ENST00000527410CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-intronENST00000372088ENST00000527354CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-intronENST00000372088ENST00000527410CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-intronENST00000494144ENST00000527354CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-intronENST00000494144ENST00000527410CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-intronENST00000543283ENST00000527354CCSER2chr10

86154692

+HINFPchr11

119005747

-
intron-intronENST00000543283ENST00000527410CCSER2chr10

86154692

+HINFPchr11

119005747

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for CCSER2-HINFP


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for CCSER2-HINFP


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:86154692/:119005747)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CCSER2

Q9H7U1

HINFP

Q9BQA5

FUNCTION: Microtubule-binding protein which might play a role in microtubule bundling. {ECO:0000250|UniProtKB:Q3UHI0}.FUNCTION: Transcriptional repressor that binds to the consensus sequence 5'-CGGACGTT-3' and to the RB1 promoter. Transcriptional activator that promotes histone H4 gene transcription at the G1/S phase transition in conjunction with NPAT. Also activates transcription of the ATM and PRKDC genes. Autoregulates its expression by associating with its own promoter. {ECO:0000269|PubMed:11553631, ECO:0000269|PubMed:14585971, ECO:0000269|PubMed:14752047, ECO:0000269|PubMed:15988025, ECO:0000269|PubMed:17163457, ECO:0000269|PubMed:17974976, ECO:0000269|PubMed:18850719}.

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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Fusion Gene Sequence for CCSER2-HINFP


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for CCSER2-HINFP


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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Related Drugs for CCSER2-HINFP


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for CCSER2-HINFP


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