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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: 8958

FusionGeneSummary for CTTN_ST8SIA1

check button Fusion gene summary
Fusion gene informationFusion gene name: CTTN_ST8SIA1
Fusion gene ID: 8958
HgeneTgene
Gene symbol

CTTN

ST8SIA1

Gene ID

2017

6489

Gene namecortactinST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1
SynonymsEMS1GD3S|SIAT8|SIAT8-A|SIAT8A|ST8SiaI
Cytomap

11q13.3

12p12.1

Type of geneprotein-codingprotein-coding
Descriptionsrc substrate cortactin1110020L01Rikamplaxinems1 sequence (mammary tumor and squamous cell carcinoma-associated (p80/85 src substrate)oncogene EMS1alpha-N-acetylneuraminide alpha-2,8-sialyltransferaseST8 alpha-N-acetylneuraminate alpha-2,8-sialyltransferase 1alpha-2,8-sialyltransferase 8Adisialoganglioside (GD3) synthaseganglioside GD3 synthaseganglioside GT3 synthaseganglioside-specific alpha
Modification date2018052220180519
UniProtAcc

Q14247

Q92185

Ensembl transtripts involved in fusion geneENST00000346329, ENST00000301843, 
ENST00000527622, ENST00000376561, 
ENST00000538675, 
ENST00000396037, 
ENST00000539510, ENST00000536558, 
ENST00000404299, ENST00000381424, 
Fusion gene scores* DoF score24 X 15 X 9=324011 X 9 X 7=693
# samples 2611
** MAII scorelog2(26/3240*10)=-3.63941028474353
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/693*10)=-2.65535182861255
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CTTN [Title/Abstract] AND ST8SIA1 [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
TCGALDBRCATCGA-GI-A2C9-01ACTTNchr11

70256066

+ST8SIA1chr12

22219369

-
* 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-intronENST00000346329ENST00000396037CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000346329ENST00000539510CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000346329ENST00000536558CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000346329ENST00000404299CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000346329ENST00000381424CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000301843ENST00000396037CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000301843ENST00000539510CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000301843ENST00000536558CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000301843ENST00000404299CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000301843ENST00000381424CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
3UTR-intronENST00000527622ENST00000396037CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
3UTR-intronENST00000527622ENST00000539510CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
3UTR-intronENST00000527622ENST00000536558CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
3UTR-intronENST00000527622ENST00000404299CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
3UTR-intronENST00000527622ENST00000381424CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000376561ENST00000396037CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000376561ENST00000539510CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000376561ENST00000536558CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000376561ENST00000404299CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
5CDS-intronENST00000376561ENST00000381424CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
intron-intronENST00000538675ENST00000396037CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
intron-intronENST00000538675ENST00000539510CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
intron-intronENST00000538675ENST00000536558CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
intron-intronENST00000538675ENST00000404299CTTNchr11

70256066

+ST8SIA1chr12

22219369

-
intron-intronENST00000538675ENST00000381424CTTNchr11

70256066

+ST8SIA1chr12

22219369

-

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FusionProtFeatures for CTTN_ST8SIA1


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

Q14247

ST8SIA1

Q92185

Contributes to the organization of the actincytoskeleton and cell shape (PubMed:21296879). Plays a role in theformation of lamellipodia and in cell migration. Plays a role inthe regulation of neuron morphology, axon growth and formation ofneuronal growth cones (By similarity). Through its interactionwith CTTNBP2, involved in the regulation of neuronal spine density(By similarity). Plays a role in the invasiveness of cancer cells,and the formation of metastases (PubMed:16636290). Plays a role infocal adhesion assembly and turnover (By similarity). In complexwith ABL1 and MYLK regulates cortical actin-based cytoskeletalrearrangement critical to sphingosine 1-phosphate (S1P)-mediatedendothelial cell (EC) barrier enhancement (PubMed:20861316). Playsa role in intracellular protein transport and endocytosis, and inmodulating the levels of potassium channels present at the cellmembrane (PubMed:17959782). Plays a role in receptor-mediatedendocytosis via clathrin-coated pits (By similarity). Required forstabilization of KCNH1 channels at the cell membrane(PubMed:23144454). {ECO:0000250|UniProtKB:Q60598,ECO:0000250|UniProtKB:Q66HL2, ECO:0000269|PubMed:16636290,ECO:0000269|PubMed:17959782, ECO:0000269|PubMed:21296879,ECO:0000269|PubMed:23144454}. Involved in the production of gangliosides GD3 and GT3from GM3; gangliosides are a subfamily of complexglycosphinglolipds that contain one or more residues of sialicacid. {ECO:0000269|PubMed:7937974, ECO:0000269|PubMed:8058740,ECO:0000269|PubMed:8195250, ECO:0000269|PubMed:8631981}.

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 CTTN_ST8SIA1


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 CTTN_ST8SIA1


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
CTTNSHANK2, WIPF1, CTNND1, CHD3, FER, WASL, ARHGAP17, CRB2, CASP3, MYLK, ACTR2, ACTR3, ARPC2, ARPC4, ARPC3, KCNA2, SYK, SDC3, SIRT1, EP300, HDAC6, RAD21, BTRC, ELAVL1, ARRB1, ARRB2, CD2AP, ASAP1, SH3PXD2A, PTK2, TINF2, ACD, CBLL1, CUL3, PXN, TNK2, GRB2, SDHAF2, SART3, THY1, PLAUR, UBL4A, SUCLG2, OXCT1, ABI1, NONO, CORO1B, DNM2, ATF2, NCF1, PAN2, NPM1, LMNA, ACTG1, APEH, ATG7, ATP6V1C1, CTNNA1, GARS, IDE, ME1, RDX, SHMT1, SHMT2, SSB, STAT1, VTA1, GSPT1, GSPT2, SARS, SNX1, SNX2, UGDH, RPA3, RPA2, RPA1, CTTN, CDC37, SPRR2A, OBSL1, EGFR, COPS7A, HEXIM1, MYO1E, USO1, NTRK1, EWSR1, CAPZA2, DBN1, FLNA, KIFC3, MLH1, MYH9, PPP1CB, IQGAP1, SYNCRIP, SYNPO, MYO5C, MYO19, NOP9, MYO18A, TRIM15, NEDD9, SNW1, KCNA3, SMURF1, YES1, CDH1, PDHA1, TES, KEAP1, TXNIPST8SIA1POTEF, RPIA, BRAT1, INTS12, NMD3, IPO13, HOOK2, INTS1, RUFY1, ZMYM2


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 CTTN_ST8SIA1


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 CTTN_ST8SIA1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCTTNC0007137Squamous cell carcinoma1CTD_human
HgeneCTTNC0023531Leukoplakia1CTD_human
HgeneCTTNC3495559Juvenile arthritis1CTD_human
TgeneST8SIA1C0023895Liver diseases1CTD_human
TgeneST8SIA1C0235032Neurotoxicity Syndromes1CTD_human