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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: 37643

FusionGeneSummary for TCTN1_FGGY

check button Fusion gene summary
Fusion gene informationFusion gene name: TCTN1_FGGY
Fusion gene ID: 37643
HgeneTgene
Gene symbol

TCTN1

FGGY

Gene ID

79600

55277

Gene nametectonic family member 1FGGY carbohydrate kinase domain containing
SynonymsJBTS13|TECT1-
Cytomap

12q24.11

1p32.1

Type of geneprotein-codingprotein-coding
Descriptiontectonic-1FGGY carbohydrate kinase domain-containing proteinD-ribulokinase
Modification date2018051920180519
UniProtAcc

Q2MV58

Q96C11

Ensembl transtripts involved in fusion geneENST00000550703, ENST00000551590, 
ENST00000397655, ENST00000471804, 
ENST00000377654, ENST00000397659, 
ENST00000551555, 
ENST00000474476, 
ENST00000371218, ENST00000303721, 
ENST00000371212, ENST00000371210, 
Fusion gene scores* DoF score3 X 3 X 2=1813 X 9 X 9=1053
# samples 214
** MAII scorelog2(2/18*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(14/1053*10)=-2.91100670408075
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TCTN1 [Title/Abstract] AND FGGY [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
TgeneFGGY

GO:0019321

pentose metabolic process

27909055

TgeneFGGY

GO:0046835

carbohydrate phosphorylation

27909055


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
TCGARVSARCTCGA-DX-A23V-01ATCTN1chr12

111052207

+FGGYchr1

59787208

+
* 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-intronENST00000550703ENST00000474476TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000550703ENST00000371218TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000550703ENST00000303721TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000550703ENST00000371212TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-intronENST00000550703ENST00000371210TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-intronENST00000551590ENST00000474476TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000551590ENST00000371218TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000551590ENST00000303721TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000551590ENST00000371212TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-intronENST00000551590ENST00000371210TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-intronENST00000397655ENST00000474476TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000397655ENST00000371218TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000397655ENST00000303721TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000397655ENST00000371212TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-intronENST00000397655ENST00000371210TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-intronENST00000471804ENST00000474476TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000471804ENST00000371218TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000471804ENST00000303721TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000471804ENST00000371212TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-intronENST00000471804ENST00000371210TCTN1chr12

111052207

+FGGYchr1

59787208

+
5UTR-intronENST00000377654ENST00000474476TCTN1chr12

111052207

+FGGYchr1

59787208

+
5UTR-5UTRENST00000377654ENST00000371218TCTN1chr12

111052207

+FGGYchr1

59787208

+
5UTR-5UTRENST00000377654ENST00000303721TCTN1chr12

111052207

+FGGYchr1

59787208

+
5UTR-5UTRENST00000377654ENST00000371212TCTN1chr12

111052207

+FGGYchr1

59787208

+
5UTR-intronENST00000377654ENST00000371210TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-intronENST00000397659ENST00000474476TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000397659ENST00000371218TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000397659ENST00000303721TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-5UTRENST00000397659ENST00000371212TCTN1chr12

111052207

+FGGYchr1

59787208

+
5CDS-intronENST00000397659ENST00000371210TCTN1chr12

111052207

+FGGYchr1

59787208

+
intron-intronENST00000551555ENST00000474476TCTN1chr12

111052207

+FGGYchr1

59787208

+
intron-5UTRENST00000551555ENST00000371218TCTN1chr12

111052207

+FGGYchr1

59787208

+
intron-5UTRENST00000551555ENST00000303721TCTN1chr12

111052207

+FGGYchr1

59787208

+
intron-5UTRENST00000551555ENST00000371212TCTN1chr12

111052207

+FGGYchr1

59787208

+
intron-intronENST00000551555ENST00000371210TCTN1chr12

111052207

+FGGYchr1

59787208

+

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FusionProtFeatures for TCTN1_FGGY


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TCTN1

Q2MV58

FGGY

Q96C11

Component of the tectonic-like complex, a complexlocalized at the transition zone of primary cilia and acting as abarrier that prevents diffusion of transmembrane proteins betweenthe cilia and plasma membranes. Regulator of Hedgehog (Hh),required for both activation and inhibition of the Hh pathway inthe patterning of the neural tube. During neural tube development,it is required for formation of the most ventral cell types andfor full Hh pathway activation. Functions in Hh signaltransduction to fully activate the pathway in the presence of highHh levels and to repress the pathway in the absence of Hh signals.Modulates Hh signal transduction downstream of SMO and RAB23 (Bysimilarity). {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 TCTN1_FGGY


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 TCTN1_FGGY


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
TCTN1IDS, TMEM25, DNASE2B, SIAE, KNG1, ASPH, BCAP31, BRI3BP, CALR, CALU, CANX, CCDC134, CKAP4, CNPY2, CNPY3, DDOST, DNAJB11, DNAJC10, DNAJC3, ERAP2, ERLEC1, ERLIN2, ERP29, GANAB, COLGALT1, GRAMD1A, HSP90B1, HSPA5, HYOU1, IKBIP, KDELC2, EMC1, P3H1, LMAN1, LRPAP1, MAGT1, MANF, MESDC2, MIA3, MINPP1, MLEC, MOGS, NENF, NUCB2, NUP210, OS9, P4HA1, P4HB, PDIA3, PDIA4, PDIA6, PPIB, PRDX4, PRKCSH, RCN1, RCN2, RPN1, RPN2, SDF2L1, SEC63, SEL1L, SEP15, SERPINH1, SLC39A7, STT3B, TMED2, TMTC3, TMX1, TOR1A, TTC13, TXNDC16, TXNDC5, UGGT1, UGGT2, AP3M1, APMAP, CHID1, CLCC1, EMC8, DDX47, DNM2, FKBP10, FKBP2, GARS, GFPT1, MAP2K1, MKL1, NCLN, NUP205, PLOD1, PLOD2, POFUT1, PRPS1, PRPS2, SEC11A, SIL1, SPCS3, SRSF2, TMED10, TMED9, EMC3, TOR1AIP1, ERO1L, ERO1LB, CC2D2A, TMEM231, B9D2, TUBB1, NPTX1, MKS1, SMOC1, MICA, GNB2, TCTN2, PSG8, SUSD4, NAAA, PSG1, TUBB8, SCGB2A2, PPOX, GML, FAM19A4, TCTN3FGGYEAF1, NSFL1C


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 TCTN1_FGGY


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 TCTN1_FGGY


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTCTN1C0431399Familial aplasia of the vermis1CTD_human;ORPHANET
HgeneTCTN1C4277682Chemical and Drug Induced Liver Injury1CTD_human