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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: 35640

FusionGeneSummary for SPEF2_SLC6A18

check button Fusion gene summary
Fusion gene informationFusion gene name: SPEF2_SLC6A18
Fusion gene ID: 35640
HgeneTgene
Gene symbol

SPEF2

SLC6A18

Gene ID

79925

348932

Gene namesperm flagellar 2solute carrier family 6 member 18
SynonymsCT122|KPL2Xtrp2
Cytomap

5p13.2

5p15.33

Type of geneprotein-codingprotein-coding
Descriptionsperm flagellar protein 2cancer/testis antigen 122testis tissue sperm-binding protein Li 47asodium-dependent neutral amino acid transporter B(0)AT3sodium channel-like proteinsodium- and chloride-dependent transporter XTRP2solute carrier family 6 (neurotransmitter transporter), member 18solute carrier family 6 (neutral amino acid transporter)
Modification date2018051920180523
UniProtAcc

Q9C093

Q96N87

Ensembl transtripts involved in fusion geneENST00000282469, ENST00000509059, 
ENST00000356031, ENST00000440995, 
ENST00000303129, 
ENST00000296821, 
ENST00000324642, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 2=8
# samples 12
** MAII scorelog2(1/1*10)=3.32192809488736log2(2/8*10)=1.32192809488736
Context

PubMed: SPEF2 [Title/Abstract] AND SLC6A18 [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
TCGARVLIHCTCGA-CC-5264-01ASPEF2chr5

35649527

+SLC6A18chr5

1242822

+
* 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-intronENST00000282469ENST00000296821SPEF2chr5

35649527

+SLC6A18chr5

1242822

+
5CDS-intronENST00000282469ENST00000324642SPEF2chr5

35649527

+SLC6A18chr5

1242822

+
5CDS-intronENST00000509059ENST00000296821SPEF2chr5

35649527

+SLC6A18chr5

1242822

+
5CDS-intronENST00000509059ENST00000324642SPEF2chr5

35649527

+SLC6A18chr5

1242822

+
5CDS-intronENST00000356031ENST00000296821SPEF2chr5

35649527

+SLC6A18chr5

1242822

+
5CDS-intronENST00000356031ENST00000324642SPEF2chr5

35649527

+SLC6A18chr5

1242822

+
5CDS-intronENST00000440995ENST00000296821SPEF2chr5

35649527

+SLC6A18chr5

1242822

+
5CDS-intronENST00000440995ENST00000324642SPEF2chr5

35649527

+SLC6A18chr5

1242822

+
intron-intronENST00000303129ENST00000296821SPEF2chr5

35649527

+SLC6A18chr5

1242822

+
intron-intronENST00000303129ENST00000324642SPEF2chr5

35649527

+SLC6A18chr5

1242822

+

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FusionProtFeatures for SPEF2_SLC6A18


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SPEF2

Q9C093

SLC6A18

Q96N87

Required for correct axoneme development. {ECO:0000250}. Functions as a sodium and chloride-dependent neutralamino acid transporter. {ECO:0000250}.

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 SPEF2_SLC6A18


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 SPEF2_SLC6A18


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
SPEF2APOA1, TSC22D2SLC6A18


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 SPEF2_SLC6A18


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 SPEF2_SLC6A18


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneSLC6A18C0020538Hypertensive disease1CTD_human