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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: 36887

FusionGeneSummary for SYN1_RDH14

check button Fusion gene summary
Fusion gene informationFusion gene name: SYN1_RDH14
Fusion gene ID: 36887
HgeneTgene
Gene symbol

SYN1

RDH14

Gene ID

6853

57665

Gene namesynapsin Iretinol dehydrogenase 14
SynonymsSYN1a|SYN1b|SYNIPAN2|SDR7C4
Cytomap

Xp11.3-p11.23

2p24.2

Type of geneprotein-codingprotein-coding
Descriptionsynapsin-1brain protein 4.1synapsin Ibretinol dehydrogenase 14alcohol dehydrogenase PAN2pancreas protein 2retinol dehydrogenase 14 (all-trans and 9-cis)retinol dehydrogenase 14 (all-trans/9-cis/11-cis)short chain dehydrogenase/reductase family 7C member 4
Modification date2018052720180523
UniProtAcc

P17600

Q9HBH5

Ensembl transtripts involved in fusion geneENST00000340666, ENST00000295987, 
ENST00000381249, ENST00000468071, 
Fusion gene scores* DoF score9 X 9 X 2=1621 X 1 X 1=1
# samples 91
** MAII scorelog2(9/162*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: SYN1 [Title/Abstract] AND RDH14 [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
ChiTaRS3.1AW965197SYN1chrX

47446105

-RDH14chr2

18736702

+
* 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-3CDSENST00000340666ENST00000381249SYN1chrX

47446105

-RDH14chr2

18736702

+
intron-5UTRENST00000340666ENST00000468071SYN1chrX

47446105

-RDH14chr2

18736702

+
intron-3CDSENST00000295987ENST00000381249SYN1chrX

47446105

-RDH14chr2

18736702

+
intron-5UTRENST00000295987ENST00000468071SYN1chrX

47446105

-RDH14chr2

18736702

+

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FusionProtFeatures for SYN1_RDH14


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SYN1

P17600

RDH14

Q9HBH5

Neuronal phosphoprotein that coats synaptic vesicles,binds to the cytoskeleton, and is believed to function in theregulation of neurotransmitter release. The complex formed withNOS1 and CAPON proteins is necessary for specific nitric-oxidfunctions at a presynaptic level. Exhibits an oxidoreductive catalytic activity towardsretinoids. Most efficient as an NADPH-dependent retinal reductase.Displays high activity toward 9-cis and all-trans-retinol. Nosteroid dehydrogenase activity detected.{ECO:0000269|PubMed:12226107}.

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 SYN1_RDH14


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 SYN1_RDH14


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 SYN1_RDH14


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneRDH14Q9HBH5DB00162Vitamin ARetinol dehydrogenase 14small moleculeapproved|nutraceutical|vet_approved

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RelatedDiseases for SYN1_RDH14


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSYN1C0011570Mental Depression4PSYGENET
HgeneSYN1C0011581Depressive disorder4PSYGENET
HgeneSYN1C0036341Schizophrenia2PSYGENET