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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: 26948

FusionGeneSummary for PHF23_RRM1

check button Fusion gene summary
Fusion gene informationFusion gene name: PHF23_RRM1
Fusion gene ID: 26948
HgeneTgene
Gene symbol

PHF23

RRM1

Gene ID

79142

6240

Gene namePHD finger protein 23ribonucleotide reductase catalytic subunit M1
SynonymshJUNE-1bR1|RIR1|RR1
Cytomap

17p13.1

11p15.4

Type of geneprotein-codingprotein-coding
DescriptionPHD finger protein 23PDH-containing protein JUNE-1PHD finger protein 23aribonucleoside-diphosphate reductase large subunitribonucleoside-diphosphate reductase subunit M1ribonucleotide reductase M1 polypeptideribonucleotide reductase, R1 subunit
Modification date2018052320180527
UniProtAcc

Q9BUL5

P23921

Ensembl transtripts involved in fusion geneENST00000320316, ENST00000571362, 
ENST00000576955, ENST00000454255, 
ENST00000570753, 
ENST00000300738, 
ENST00000423050, ENST00000534285, 
ENST00000537197, ENST00000528470, 
Fusion gene scores* DoF score2 X 2 X 2=86 X 5 X 3=90
# samples 26
** MAII scorelog2(2/8*10)=1.32192809488736log2(6/90*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: PHF23 [Title/Abstract] AND RRM1 [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

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
ChiTaRS3.1AU125246PHF23chr17

7139380

-RRM1chr11

4144413

+
* 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-3CDSENST00000320316ENST00000300738PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000320316ENST00000423050PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000320316ENST00000534285PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000320316ENST00000537197PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3UTRENST00000320316ENST00000528470PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000571362ENST00000300738PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000571362ENST00000423050PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000571362ENST00000534285PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000571362ENST00000537197PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3UTRENST00000571362ENST00000528470PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000576955ENST00000300738PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000576955ENST00000423050PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000576955ENST00000534285PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000576955ENST00000537197PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3UTRENST00000576955ENST00000528470PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000454255ENST00000300738PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000454255ENST00000423050PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000454255ENST00000534285PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000454255ENST00000537197PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3UTRENST00000454255ENST00000528470PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000570753ENST00000300738PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000570753ENST00000423050PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000570753ENST00000534285PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3CDSENST00000570753ENST00000537197PHF23chr17

7139380

-RRM1chr11

4144413

+
intron-3UTRENST00000570753ENST00000528470PHF23chr17

7139380

-RRM1chr11

4144413

+

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FusionProtFeatures for PHF23_RRM1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
PHF23

Q9BUL5

RRM1

P23921

Acts as a negative regulator of autophagy, throughpromoting ubiquitination and degradation of LRSAM1, an E3ubiquitin ligase that promotes autophagy in response to starvationor infecting bacteria. {ECO:0000269|PubMed:25484098}. Provides the precursors necessary for DNA synthesis.Catalyzes the biosynthesis of deoxyribonucleotides from thecorresponding ribonucleotides.

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 PHF23_RRM1


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 PHF23_RRM1


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 PHF23_RRM1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneRRM1P23921DB00441GemcitabineRibonucleoside-diphosphate reductase large subunitsmall moleculeapproved
TgeneRRM1P23921DB01005HydroxyureaRibonucleoside-diphosphate reductase large subunitsmall moleculeapproved
TgeneRRM1P23921DB01073FludarabineRibonucleoside-diphosphate reductase large subunitsmall moleculeapproved
TgeneRRM1P23921DB00242CladribineRibonucleoside-diphosphate reductase large subunitsmall moleculeapproved|investigational
TgeneRRM1P23921DB00631ClofarabineRibonucleoside-diphosphate reductase large subunitsmall moleculeapproved|investigational

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RelatedDiseases for PHF23_RRM1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneRRM1C0007131Non-Small Cell Lung Carcinoma1CTD_human
TgeneRRM1C0027794Neural Tube Defects1CTD_human
TgeneRRM1C0206686Adrenocortical carcinoma1CTD_human
TgeneRRM1C2239176Liver carcinoma1CTD_human