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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:CLCC1-KREMEN1 (FusionGDB2 ID:16971)

Fusion Gene Summary for CLCC1-KREMEN1

check button Fusion gene summary
Fusion gene informationFusion gene name: CLCC1-KREMEN1
Fusion gene ID: 16971
HgeneTgene
Gene symbol

CLCC1

KREMEN1

Gene ID

23155

83999

Gene namechloride channel CLIC like 1kringle containing transmembrane protein 1
SynonymsMCLCECTD13|KREMEN|KRM1
Cytomap

1p13.3

22q12.1

Type of geneprotein-codingprotein-coding
Descriptionchloride channel CLIC-like protein 1Mid-1-related chloride channel protein 1kremen protein 1dickkopf receptorkringle domain-containing transmembrane protein 1kringle-coding gene marking the eye and the nosekringle-containing protein marking the eye and the nose
Modification date2020031320200313
UniProtAcc

Q96S66

Q96MU8

Ensembl transtripts involved in fusion geneENST00000302500, ENST00000348264, 
ENST00000356970, ENST00000369968, 
ENST00000369969, ENST00000369970, 
ENST00000369971, ENST00000369976, 
ENST00000415331, ENST00000482889, 
ENST00000400335, ENST00000400338, 
ENST00000327813, ENST00000407188, 
ENST00000479755, 
Fusion gene scores* DoF score4 X 4 X 2=325 X 9 X 5=225
# samples 49
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(9/225*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CLCC1 [Title/Abstract] AND KREMEN1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCLCC1(109495192)-KREMEN1(29538667), # 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

check buttonFusion gene breakpoints across CLCC1 (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 KREMEN1 (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/AAW073990CLCC1chr1

109495192

+KREMEN1chr22

29538667

-


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Fusion Gene ORF analysis for CLCC1-KREMEN1

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-3UTRENST00000302500ENST00000400335CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000302500ENST00000400338CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000348264ENST00000400335CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000348264ENST00000400338CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000356970ENST00000400335CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000356970ENST00000400338CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000369968ENST00000400335CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000369968ENST00000400338CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000369969ENST00000400335CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000369969ENST00000400338CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000369970ENST00000400335CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000369970ENST00000400338CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000369971ENST00000400335CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000369971ENST00000400338CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000369976ENST00000400335CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000369976ENST00000400338CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000415331ENST00000400335CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000415331ENST00000400338CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000482889ENST00000400335CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-3UTRENST00000482889ENST00000400338CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000302500ENST00000327813CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000302500ENST00000407188CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000302500ENST00000479755CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000348264ENST00000327813CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000348264ENST00000407188CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000348264ENST00000479755CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000356970ENST00000327813CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000356970ENST00000407188CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000356970ENST00000479755CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369968ENST00000327813CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369968ENST00000407188CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369968ENST00000479755CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369969ENST00000327813CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369969ENST00000407188CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369969ENST00000479755CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369970ENST00000327813CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369970ENST00000407188CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369970ENST00000479755CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369971ENST00000327813CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369971ENST00000407188CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369971ENST00000479755CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369976ENST00000327813CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369976ENST00000407188CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000369976ENST00000479755CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000415331ENST00000327813CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000415331ENST00000407188CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000415331ENST00000479755CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000482889ENST00000327813CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000482889ENST00000407188CLCC1chr1

109495192

+KREMEN1chr22

29538667

-
intron-intronENST00000482889ENST00000479755CLCC1chr1

109495192

+KREMEN1chr22

29538667

-

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 CLCC1-KREMEN1


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 CLCC1-KREMEN1


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/:109495192/:29538667)
- 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
CLCC1

Q96S66

KREMEN1

Q96MU8

FUNCTION: Seems to act as a chloride ion channel (PubMed:30157172). Plays a role in retina development (PubMed:30157172). {ECO:0000269|PubMed:30157172}.FUNCTION: Receptor for Dickkopf proteins. Cooperates with DKK1/2 to inhibit Wnt/beta-catenin signaling by promoting the endocytosis of Wnt receptors LRP5 and LRP6. In the absence of DKK1, potentiates Wnt-beta-catenin signaling by maintaining LRP5 or LRP6 at the cell membrane. Can trigger apoptosis in a Wnt-independent manner and this apoptotic activity is inhibited upon binding of the ligand DKK1. Plays a role in limb development; attenuates Wnt signaling in the developing limb to allow normal limb patterning and can also negatively regulate bone formation. Modulates cell fate decisions in the developing cochlea with an inhibitory role in hair cell fate specification. {ECO:0000250|UniProtKB:Q90Y90, ECO:0000250|UniProtKB:Q99N43}.

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 CLCC1-KREMEN1


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 CLCC1-KREMEN1


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 CLCC1-KREMEN1


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 CLCC1-KREMEN1


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