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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: 35251

FusionGeneSummary for SNX14_EYS

check button Fusion gene summary
Fusion gene informationFusion gene name: SNX14_EYS
Fusion gene ID: 35251
HgeneTgene
Gene symbol

SNX14

EYS

Gene ID

57231

346007

Gene namesorting nexin 14eyes shut homolog (Drosophila)
SynonymsRGS-PX2|SCAR20C6orf178|C6orf179|C6orf180|EGFL10|EGFL11|RP25|SPAM|bA166P24.2|bA307F22.3|bA74E24.1|dJ1018A4.2|dJ22I17.2|dJ303F19.1
Cytomap

6q14.3

6q12

Type of geneprotein-codingprotein-coding
Descriptionsorting nexin-14protein eyes shut homologEGF-like-domain, multiple 10EGF-like-domain, multiple 11epidermal growth factor-like protein 10epidermal growth factor-like protein 11protein spacemaker homolog
Modification date2018051920180519
UniProtAcc

Q9Y5W7

Q5T1H1

Ensembl transtripts involved in fusion geneENST00000346348, ENST00000314673, 
ENST00000513865, ENST00000505648, 
ENST00000508980, ENST00000369627, 
ENST00000503581, ENST00000370621, 
ENST00000370616, ENST00000393380, 
ENST00000342421, ENST00000370618, 
ENST00000486069, 
Fusion gene scores* DoF score6 X 2 X 4=4826 X 15 X 12=4680
# samples 627
** MAII scorelog2(6/48*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(27/4680*10)=-4.11547721741994
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SNX14 [Title/Abstract] AND EYS [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
TCGARVBRCATCGA-D8-A73W-01ASNX14chr6

86303297

-EYSchr6

66205886

-
* 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
5CDS-5UTRENST00000346348ENST00000503581SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000346348ENST00000370621SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-intronENST00000346348ENST00000370616SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000346348ENST00000393380SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000346348ENST00000342421SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000346348ENST00000370618SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-intronENST00000346348ENST00000486069SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000314673ENST00000503581SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000314673ENST00000370621SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-intronENST00000314673ENST00000370616SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000314673ENST00000393380SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000314673ENST00000342421SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000314673ENST00000370618SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-intronENST00000314673ENST00000486069SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000513865ENST00000503581SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000513865ENST00000370621SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-intronENST00000513865ENST00000370616SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000513865ENST00000393380SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000513865ENST00000342421SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000513865ENST00000370618SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-intronENST00000513865ENST00000486069SNX14chr6

86303297

-EYSchr6

66205886

-
intron-5UTRENST00000505648ENST00000503581SNX14chr6

86303297

-EYSchr6

66205886

-
intron-5UTRENST00000505648ENST00000370621SNX14chr6

86303297

-EYSchr6

66205886

-
intron-intronENST00000505648ENST00000370616SNX14chr6

86303297

-EYSchr6

66205886

-
intron-5UTRENST00000505648ENST00000393380SNX14chr6

86303297

-EYSchr6

66205886

-
intron-5UTRENST00000505648ENST00000342421SNX14chr6

86303297

-EYSchr6

66205886

-
intron-5UTRENST00000505648ENST00000370618SNX14chr6

86303297

-EYSchr6

66205886

-
intron-intronENST00000505648ENST00000486069SNX14chr6

86303297

-EYSchr6

66205886

-
intron-5UTRENST00000508980ENST00000503581SNX14chr6

86303297

-EYSchr6

66205886

-
intron-5UTRENST00000508980ENST00000370621SNX14chr6

86303297

-EYSchr6

66205886

-
intron-intronENST00000508980ENST00000370616SNX14chr6

86303297

-EYSchr6

66205886

-
intron-5UTRENST00000508980ENST00000393380SNX14chr6

86303297

-EYSchr6

66205886

-
intron-5UTRENST00000508980ENST00000342421SNX14chr6

86303297

-EYSchr6

66205886

-
intron-5UTRENST00000508980ENST00000370618SNX14chr6

86303297

-EYSchr6

66205886

-
intron-intronENST00000508980ENST00000486069SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000369627ENST00000503581SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000369627ENST00000370621SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-intronENST00000369627ENST00000370616SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000369627ENST00000393380SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000369627ENST00000342421SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-5UTRENST00000369627ENST00000370618SNX14chr6

86303297

-EYSchr6

66205886

-
5CDS-intronENST00000369627ENST00000486069SNX14chr6

86303297

-EYSchr6

66205886

-

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FusionProtFeatures for SNX14_EYS


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SNX14

Q9Y5W7

EYS

Q5T1H1

Plays a role in maintaining normal neuronal excitabilityand synaptic transmission. May be involved in several stages ofintracellular trafficking (By similarity). Required forautophagosome clearance, possibly by mediating the fusion oflysosomes with autophagosomes (Probable). Bindsphosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2), a keycomponent of late endosomes/lysosomes (PubMed:25848753). Does notbind phosphatidylinositol 3-phosphate (PtdIns(3P))(PubMed:25848753, PubMed:25148684). {ECO:0000250|UniProtKB:Q8BHY8,ECO:0000269|PubMed:25148684, ECO:0000269|PubMed:25848753,ECO:0000305|PubMed:25848753}.

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 SNX14_EYS


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 SNX14_EYS


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
SNX14HNF1A, SHMT2, NXF1, TEX264, MCOLN3, IQCF1, CHRNA9, ATL3, TSPAN2, ZNRF4, CNGA3, IPPK, SLC4A8, SIGLECL1, PCDHGA5, TLR5, C3AR1, PMEL, FSHR, SLC17A2, PTGIREYSEGFR


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 SNX14_EYS


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 SNX14_EYS


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSNX14C0007758Cerebellar Ataxia1CTD_human
HgeneSNX14C3714756Intellectual Disability1CTD_human
TgeneEYSC1864446Retinitis Pigmentosa 252CTD_human;UNIPROT
TgeneEYSC0035334Retinitis Pigmentosa1CTD_human;ORPHANET