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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: 41269

FusionGeneSummary for UTRN_NFIA

check button Fusion gene summary
Fusion gene informationFusion gene name: UTRN_NFIA
Fusion gene ID: 41269
HgeneTgene
Gene symbol

UTRN

NFIA

Gene ID

7402

4774

Gene nameutrophinnuclear factor I A
SynonymsDMDL|DRP|DRP1BRMUTD|CTF|NF-I/A|NF1-A|NFI-A|NFI-L
Cytomap

6q24.2

1p31.3

Type of geneprotein-codingprotein-coding
DescriptionutrophinDRP-1dystrophin-related protein 1nuclear factor 1 A-typeCCAAT-box-binding transcription factorTGGCA-binding protein
Modification date2018051920180523
UniProtAcc

P46939

Q12857

Ensembl transtripts involved in fusion geneENST00000367545, ENST00000367526, 
ENST00000480333, 
ENST00000371191, 
ENST00000407417, ENST00000479364, 
ENST00000371189, ENST00000403491, 
ENST00000371187, ENST00000485903, 
ENST00000371185, ENST00000371184, 
ENST00000357977, 
Fusion gene scores* DoF score24 X 22 X 7=369611 X 13 X 6=858
# samples 2515
** MAII scorelog2(25/3696*10)=-3.88596475675397
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/858*10)=-2.51601514700366
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: UTRN [Title/Abstract] AND NFIA [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
TgeneNFIA

GO:0045944

positive regulation of transcription by RNA polymerase II

17010934


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
ChiTaRS3.1AU142016UTRNchr6

144766736

+NFIAchr1

61926695

+
* 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-intronENST00000367545ENST00000371191UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367545ENST00000407417UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367545ENST00000479364UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367545ENST00000371189UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-3UTRENST00000367545ENST00000403491UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367545ENST00000371187UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367545ENST00000485903UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367545ENST00000371185UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367545ENST00000371184UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367545ENST00000357977UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367526ENST00000371191UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367526ENST00000407417UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367526ENST00000479364UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367526ENST00000371189UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-3UTRENST00000367526ENST00000403491UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367526ENST00000371187UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367526ENST00000485903UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367526ENST00000371185UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367526ENST00000371184UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000367526ENST00000357977UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000480333ENST00000371191UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000480333ENST00000407417UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000480333ENST00000479364UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000480333ENST00000371189UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-3UTRENST00000480333ENST00000403491UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000480333ENST00000371187UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000480333ENST00000485903UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000480333ENST00000371185UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000480333ENST00000371184UTRNchr6

144766736

+NFIAchr1

61926695

+
intron-intronENST00000480333ENST00000357977UTRNchr6

144766736

+NFIAchr1

61926695

+

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FusionProtFeatures for UTRN_NFIA


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

P46939

NFIA

Q12857

May play a role in anchoring the cytoskeleton to theplasma membrane. {ECO:0000250}. Recognizes and binds the palindromic sequence 5'-TTGGCNNNNNGCCAA-3' present in viral and cellular promoters and inthe origin of replication of adenovirus type 2. These proteins areindividually capable of activating transcription and replication.

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 UTRN_NFIA


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 UTRN_NFIA


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 UTRN_NFIA


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneUTRNP46939DB01593ZincUtrophinsmall moleculeapproved|investigational

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RelatedDiseases for UTRN_NFIA


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