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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:ZCCHC7-MICU1 (FusionGDB2 ID:100019)

Fusion Gene Summary for ZCCHC7-MICU1

check button Fusion gene summary
Fusion gene informationFusion gene name: ZCCHC7-MICU1
Fusion gene ID: 100019
HgeneTgene
Gene symbol

ZCCHC7

MICU1

Gene ID

84186

10367

Gene namezinc finger CCHC-type containing 7mitochondrial calcium uptake 1
SynonymsAIR1|HSPC086CALC|CBARA1|EFHA3|MPXPS|ara CALC
Cytomap

9p13.2

10q22.1

Type of geneprotein-codingprotein-coding
Descriptionzinc finger CCHC domain-containing protein 7TRAMP-like complex RNA-binding factor ZCCHC7zinc finger, CCHC domain containing 7calcium uptake protein 1, mitochondrialatopy-related autoantigen CALCcalcium-binding atopy-related autoantigen 1
Modification date2020032020200313
UniProtAcc.

Q9BPX6

Ensembl transtripts involved in fusion geneENST00000336755, ENST00000534928, 
ENST00000461038, ENST00000322831, 
ENST00000401998, ENST00000361114, 
ENST00000398761, ENST00000418483, 
ENST00000398763, ENST00000604025, 
Fusion gene scores* DoF score29 X 11 X 11=350922 X 15 X 11=3630
# samples 2930
** MAII scorelog2(29/3509*10)=-3.59693514238723
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(30/3630*10)=-3.59693514238723
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZCCHC7 [Title/Abstract] AND MICU1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointZCCHC7(37126939)-MICU1(74183129), # samples:1
Anticipated loss of major functional domain due to fusion event.ZCCHC7-MICU1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
ZCCHC7-MICU1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* 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
TgeneMICU1

GO:0006851

mitochondrial calcium ion transmembrane transport

24560927

TgeneMICU1

GO:0051260

protein homooligomerization

24514027

TgeneMICU1

GO:0051561

positive regulation of mitochondrial calcium ion concentration

24560927

TgeneMICU1

GO:0070509

calcium ion import

20693986


check buttonFusion gene breakpoints across ZCCHC7 (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 MICU1 (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
ChimerDB4BRCATCGA-E9-A243ZCCHC7chr9

37126939

+MICU1chr10

74183129

-


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Fusion Gene ORF analysis for ZCCHC7-MICU1

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
Frame-shiftENST00000336755ENST00000401998ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
Frame-shiftENST00000336755ENST00000361114ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
Frame-shiftENST00000336755ENST00000398761ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
Frame-shiftENST00000336755ENST00000418483ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
Frame-shiftENST00000336755ENST00000398763ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
5CDS-intronENST00000336755ENST00000604025ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
intron-3CDSENST00000534928ENST00000401998ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
intron-3CDSENST00000534928ENST00000361114ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
intron-3CDSENST00000534928ENST00000398761ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
intron-3CDSENST00000534928ENST00000418483ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
intron-3CDSENST00000534928ENST00000398763ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
intron-intronENST00000534928ENST00000604025ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
3UTR-3CDSENST00000461038ENST00000401998ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
3UTR-3CDSENST00000461038ENST00000361114ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
3UTR-3CDSENST00000461038ENST00000398761ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
3UTR-3CDSENST00000461038ENST00000418483ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
3UTR-3CDSENST00000461038ENST00000398763ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
3UTR-intronENST00000461038ENST00000604025ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
Frame-shiftENST00000322831ENST00000401998ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
Frame-shiftENST00000322831ENST00000361114ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
Frame-shiftENST00000322831ENST00000398761ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
Frame-shiftENST00000322831ENST00000418483ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
Frame-shiftENST00000322831ENST00000398763ZCCHC7chr9

37126939

+MICU1chr10

74183129

-
5CDS-intronENST00000322831ENST00000604025ZCCHC7chr9

37126939

+MICU1chr10

74183129

-

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 ZCCHC7-MICU1


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 ZCCHC7-MICU1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.MICU1

Q9BPX6

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Key regulator of mitochondrial calcium uniporter (MCU) that senses calcium level via its EF-hand domains (PubMed:20693986, PubMed:23101630, PubMed:23747253, PubMed:24313810, PubMed:24332854, PubMed:24503055, PubMed:24560927, PubMed:26341627, PubMed:26903221, PubMed:27099988). MICU1 and MICU2 form a disulfide-linked heterodimer that stimulates and inhibits MCU activity, depending on the concentration of calcium. MICU1 acts both as an activator or inhibitor of mitochondrial calcium uptake (PubMed:26903221). Acts as a gatekeeper of MCU at low concentration of calcium, preventing channel opening (PubMed:26903221). Enhances MCU opening at high calcium concentration, allowing a rapid response of mitochondria to calcium signals generated in the cytoplasm (PubMed:24560927, PubMed:26903221). Regulates glucose-dependent insulin secretion in pancreatic beta-cells by regulating mitochondrial calcium uptake (PubMed:22904319). Induces T-helper 1-mediated autoreactivity, which is accompanied by the release of IFNG (PubMed:16002733). {ECO:0000269|PubMed:16002733, ECO:0000269|PubMed:20693986, ECO:0000269|PubMed:22904319, ECO:0000269|PubMed:23101630, ECO:0000269|PubMed:23747253, ECO:0000269|PubMed:24313810, ECO:0000269|PubMed:24332854, ECO:0000269|PubMed:24503055, ECO:0000269|PubMed:24560927, ECO:0000269|PubMed:26341627, ECO:0000269|PubMed:26903221, ECO:0000269|PubMed:27099988}.

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 ZCCHC7-MICU1


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 ZCCHC7-MICU1


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 ZCCHC7-MICU1


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 ZCCHC7-MICU1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneMICU1C3810285MYOPATHY WITH EXTRAPYRAMIDAL SIGNS2CTD_human;GENOMICS_ENGLAND;ORPHANET
TgeneMICU1C0004782Basal Ganglia Diseases1CTD_human
TgeneMICU1C0015371Extrapyramidal Disorders1CTD_human
TgeneMICU1C0023186Learning Disorders1CTD_human
TgeneMICU1C0026650Movement Disorders1CTD_human
TgeneMICU1C0026848Myopathy1CTD_human
TgeneMICU1C0266487Etat Marbre1CTD_human
TgeneMICU1C0750951Lenticulostriate Disorders1CTD_human
TgeneMICU1C0751262Adult Learning Disorders1CTD_human
TgeneMICU1C0751263Learning Disturbance1CTD_human
TgeneMICU1C0751265Learning Disabilities1CTD_human
TgeneMICU1C1330966Developmental Academic Disorder1CTD_human