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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: 18066

FusionGeneSummary for JMJD1C_EGR2

check button Fusion gene summary
Fusion gene informationFusion gene name: JMJD1C_EGR2
Fusion gene ID: 18066
HgeneTgene
Gene symbol

JMJD1C

EGR2

Gene ID

221037

1959

Gene namejumonji domain containing 1Cearly growth response 2
SynonymsKDM3C|TRIP-8|TRIP8AT591|CMT1D|CMT4E|KROX20
Cytomap

10q21.3

10q21.3

Type of geneprotein-codingprotein-coding
Descriptionprobable JmjC domain-containing histone demethylation protein 2CTR-interacting protein 8thyroid hormone receptor interactor 8thyroid receptor-interacting protein 8E3 SUMO-protein ligase EGR2E3 SUMO-protein transferase ERG2KROX-20, Drosophila, homolog (early growth response-2)early growth response protein 2zinc finger protein Krox-20
Modification date2018052320180523
UniProtAcc

Q15652

P11161

Ensembl transtripts involved in fusion geneENST00000399262, ENST00000402544, 
ENST00000399251, ENST00000542921, 
ENST00000489372, 
ENST00000493899, 
ENST00000242480, ENST00000411732, 
ENST00000439032, 
Fusion gene scores* DoF score13 X 8 X 6=6241 X 1 X 1=1
# samples 131
** MAII scorelog2(13/624*10)=-2.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: JMJD1C [Title/Abstract] AND EGR2 [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
TgeneEGR2

GO:0045944

positive regulation of transcription by RNA polymerase II

12687019


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
TCGALDOVTCGA-24-1928-01AJMJD1Cchr10

65281498

-EGR2chr10

64575729

-
* 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
intron-5UTRENST00000399262ENST00000493899JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000399262ENST00000242480JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000399262ENST00000411732JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000399262ENST00000439032JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000402544ENST00000493899JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000402544ENST00000242480JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000402544ENST00000411732JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000402544ENST00000439032JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000399251ENST00000493899JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000399251ENST00000242480JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000399251ENST00000411732JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000399251ENST00000439032JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000542921ENST00000493899JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000542921ENST00000242480JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000542921ENST00000411732JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000542921ENST00000439032JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000489372ENST00000493899JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000489372ENST00000242480JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000489372ENST00000411732JMJD1Cchr10

65281498

-EGR2chr10

64575729

-
intron-5UTRENST00000489372ENST00000439032JMJD1Cchr10

65281498

-EGR2chr10

64575729

-

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FusionProtFeatures for JMJD1C_EGR2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
JMJD1C

Q15652

EGR2

P11161

Sequence-specific DNA-binding transcription factor.Binds to two specific DNA sites located in the promoter region ofHOXA4. {ECO:0000269|PubMed:21836637}. E3 SUMO-protein ligase helping SUMO1 conjugation to itscoregulators NAB1 and NAB2, whose sumoylation down-regulates EGR2own transcriptional activity. {ECO:0000269|PubMed:21836637}.

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 JMJD1C_EGR2


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 JMJD1C_EGR2


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
JMJD1CVHL, ESR2, PPARG, NUDT21, TK1, GADD45A, AR, RNF8, RNF168, MT2A, PSMC1, SRPK2, RBPJ, NR3C1, TXNIPEGR2HCFC1, ACP5, MED31, NFATC1, UBE2I, NAB2, WWP2, DTX1, SRA1, HN1L, BPGM, NDUFS2, RBM15B, RIMKLB, RPL7L1, SNAI1, DNMT3L


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 JMJD1C_EGR2


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 JMJD1C_EGR2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneJMJD1CC0004352Autistic Disorder1CTD_human
HgeneJMJD1CC0010606Adenoid Cystic Carcinoma1CTD_human
HgeneJMJD1CC3495559Juvenile arthritis1CTD_human
TgeneEGR2C1843247Charcot-Marie-Tooth disease, Type 1D (disorder)5CTD_human;ORPHANET;UNIPROT
TgeneEGR2C0011195Dejerine-Sottas Disease (disorder)3ORPHANET;UNIPROT
TgeneEGR2C0036341Schizophrenia3PSYGENET
TgeneEGR2C0005586Bipolar Disorder2PSYGENET
TgeneEGR2C0004352Autistic Disorder1CTD_human
TgeneEGR2C0035372Rett Syndrome1CTD_human
TgeneEGR2C0151744Myocardial Ischemia1CTD_human
TgeneEGR2C0393818Congenital hypomyelinating neuropathy1CTD_human;ORPHANET;UNIPROT
TgeneEGR2C0553580Ewings sarcoma1CTD_human