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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: 43262

FusionGeneSummary for ZNF394_RIN3

check button Fusion gene summary
Fusion gene informationFusion gene name: ZNF394_RIN3
Fusion gene ID: 43262
HgeneTgene
Gene symbol

ZNF394

RIN3

Gene ID

84124

79890

Gene namezinc finger protein 394Ras and Rab interactor 3
SynonymsZKSCAN14|ZSCAN46-
Cytomap

7q22.1

14q32.12

Type of geneprotein-codingprotein-coding
Descriptionzinc finger protein 394zinc finger protein 99zinc finger protein with KRAB and SCAN domains 14ras and Rab interactor 3RAB5 interacting protein 3ras interaction/interference protein 3
Modification date2018052320180522
UniProtAcc

Q53GI3

Q8TB24

Ensembl transtripts involved in fusion geneENST00000337673, ENST00000426306, 
ENST00000394177, 
ENST00000216487, 
ENST00000418924, ENST00000557762, 
Fusion gene scores* DoF score1 X 1 X 1=17 X 8 X 5=280
# samples 110
** MAII scorelog2(1/1*10)=3.32192809488736log2(10/280*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ZNF394 [Title/Abstract] AND RIN3 [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
ChiTaRS3.1BC062588ZNF394chr7

99095461

-RIN3chr14

93120621

+
* 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-intronENST00000337673ENST00000216487ZNF394chr7

99095461

-RIN3chr14

93120621

+
intron-intronENST00000337673ENST00000418924ZNF394chr7

99095461

-RIN3chr14

93120621

+
intron-intronENST00000337673ENST00000557762ZNF394chr7

99095461

-RIN3chr14

93120621

+
intron-intronENST00000426306ENST00000216487ZNF394chr7

99095461

-RIN3chr14

93120621

+
intron-intronENST00000426306ENST00000418924ZNF394chr7

99095461

-RIN3chr14

93120621

+
intron-intronENST00000426306ENST00000557762ZNF394chr7

99095461

-RIN3chr14

93120621

+
intron-intronENST00000394177ENST00000216487ZNF394chr7

99095461

-RIN3chr14

93120621

+
intron-intronENST00000394177ENST00000418924ZNF394chr7

99095461

-RIN3chr14

93120621

+
intron-intronENST00000394177ENST00000557762ZNF394chr7

99095461

-RIN3chr14

93120621

+

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FusionProtFeatures for ZNF394_RIN3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ZNF394

Q53GI3

RIN3

Q8TB24

May be involved in transcriptional regulation. Ras effector protein that functions as a guaninenucleotide exchange (GEF) for RAB5B and RAB31, by exchanging boundGDP for free GTP. Required for normal RAB31 function.{ECO:0000269|PubMed:12972505, ECO:0000269|PubMed:21586568}.

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 ZNF394_RIN3


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 ZNF394_RIN3


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 ZNF394_RIN3


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 ZNF394_RIN3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneRIN3C0029401Osteitis Deformans1CTD_human