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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: 19001

FusionGeneSummary for KLHDC3_ATN1

check button Fusion gene summary
Fusion gene informationFusion gene name: KLHDC3_ATN1
Fusion gene ID: 19001
HgeneTgene
Gene symbol

KLHDC3

ATN1

Gene ID

116138

1822

Gene namekelch domain containing 3atrophin 1
SynonymsPEAS|dJ20C7.3B37|D12S755E|DRPLA|HRS|NOD
Cytomap

6p21.1

12p13.31

Type of geneprotein-codingprotein-coding
Descriptionkelch domain-containing protein 3testis intracellular mediator proteinatrophin-1dentatorubral-pallidoluysian atrophy protein
Modification date2018052320180523
UniProtAcc

Q9BQ90

P54259

Ensembl transtripts involved in fusion geneENST00000326974, ENST00000244670, 
ENST00000332245, 
ENST00000356654, 
ENST00000396684, 
Fusion gene scores* DoF score3 X 4 X 1=128 X 8 X 2=128
# samples 48
** MAII scorelog2(4/12*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(8/128*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: KLHDC3 [Title/Abstract] AND ATN1 [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
TgeneATN1

GO:0000122

negative regulation of transcription by RNA polymerase II

10973986

TgeneATN1

GO:0051402

neuron apoptotic process

10085113


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
ChiTaRS3.1L10377KLHDC3chr6

42988543

+ATN1chr12

7045837

+
* 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-3CDSENST00000326974ENST00000356654KLHDC3chr6

42988543

+ATN1chr12

7045837

+
3UTR-3CDSENST00000326974ENST00000396684KLHDC3chr6

42988543

+ATN1chr12

7045837

+
3UTR-3CDSENST00000244670ENST00000356654KLHDC3chr6

42988543

+ATN1chr12

7045837

+
3UTR-3CDSENST00000244670ENST00000396684KLHDC3chr6

42988543

+ATN1chr12

7045837

+
3UTR-3CDSENST00000332245ENST00000356654KLHDC3chr6

42988543

+ATN1chr12

7045837

+
3UTR-3CDSENST00000332245ENST00000396684KLHDC3chr6

42988543

+ATN1chr12

7045837

+

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FusionProtFeatures for KLHDC3_ATN1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
KLHDC3

Q9BQ90

ATN1

P54259

May be involved in meiotic recombination process. Transcriptional corepressor. Recruits NR2E1 to represstranscription. Promotes vascular smooth cell (VSMC) migration andorientation (By similarity). Corepressor of MTG8 transcriptionalrepression. Has some intrinsic repression activity which isindependent of the number of poly-Gln (polyQ) repeats.{ECO:0000250, ECO:0000269|PubMed:10085113,ECO:0000269|PubMed:10973986}.

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 KLHDC3_ATN1


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 KLHDC3_ATN1


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 KLHDC3_ATN1


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 KLHDC3_ATN1


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