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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: 14161

FusionGeneSummary for FZD3_CTBP1

check button Fusion gene summary
Fusion gene informationFusion gene name: FZD3_CTBP1
Fusion gene ID: 14161
HgeneTgene
Gene symbol

FZD3

CTBP1

Gene ID

7976

1487

Gene namefrizzled class receptor 3C-terminal binding protein 1
SynonymsFz-3BARS|HADDTS
Cytomap

8p21.1

4p16.3

Type of geneprotein-codingprotein-coding
Descriptionfrizzled-3frizzled 3, seven transmembrane spanning receptorfrizzled family receptor 3frizzled homolog 3C-terminal-binding protein 1brefeldin A-ribosylated substrate
Modification date2018052320180522
UniProtAcc

Q9NPG1

Q13363

Ensembl transtripts involved in fusion geneENST00000537916, ENST00000240093, 
ENST00000517911, 
ENST00000382952, 
ENST00000290921, ENST00000510568, 
ENST00000515690, 
Fusion gene scores* DoF score2 X 2 X 1=48 X 7 X 8=448
# samples 212
** MAII scorelog2(2/4*10)=2.32192809488736log2(12/448*10)=-1.90046432644909
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FZD3 [Title/Abstract] AND CTBP1 [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
HgeneFZD3

GO:0060070

canonical Wnt signaling pathway

20802536


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
ChiTaRS3.1DB495584FZD3chr8

28351860

+CTBP1chr4

1235309

-
* 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
5UTR-5UTRENST00000537916ENST00000382952FZD3chr8

28351860

+CTBP1chr4

1235309

-
5UTR-intronENST00000537916ENST00000290921FZD3chr8

28351860

+CTBP1chr4

1235309

-
5UTR-5UTRENST00000537916ENST00000510568FZD3chr8

28351860

+CTBP1chr4

1235309

-
5UTR-intronENST00000537916ENST00000515690FZD3chr8

28351860

+CTBP1chr4

1235309

-
5UTR-5UTRENST00000240093ENST00000382952FZD3chr8

28351860

+CTBP1chr4

1235309

-
5UTR-intronENST00000240093ENST00000290921FZD3chr8

28351860

+CTBP1chr4

1235309

-
5UTR-5UTRENST00000240093ENST00000510568FZD3chr8

28351860

+CTBP1chr4

1235309

-
5UTR-intronENST00000240093ENST00000515690FZD3chr8

28351860

+CTBP1chr4

1235309

-
intron-5UTRENST00000517911ENST00000382952FZD3chr8

28351860

+CTBP1chr4

1235309

-
intron-intronENST00000517911ENST00000290921FZD3chr8

28351860

+CTBP1chr4

1235309

-
intron-5UTRENST00000517911ENST00000510568FZD3chr8

28351860

+CTBP1chr4

1235309

-
intron-intronENST00000517911ENST00000515690FZD3chr8

28351860

+CTBP1chr4

1235309

-

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FusionProtFeatures for FZD3_CTBP1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FZD3

Q9NPG1

CTBP1

Q13363

Receptor for Wnt proteins. Most of frizzled receptorsare coupled to the beta-catenin canonical signaling pathway, whichleads to the activation of disheveled proteins, inhibition of GSK-3 kinase, nuclear accumulation of beta-catenin and activation ofWnt target genes. A second signaling pathway involving PKC andcalcium fluxes has been seen for some family members, but it isnot yet clear if it represents a distinct pathway or if it can beintegrated in the canonical pathway, as PKC seems to be requiredfor Wnt-mediated inactivation of GSK-3 kinase. Both pathways seemto involve interactions with G-proteins. Activation by Wnt5Astimulates PKC activity via a G-protein-dependent mechanism.Involved in transduction and intercellular transmission ofpolarity information during tissue morphogenesis and/or indifferentiated tissues. Plays a role in controlling early axongrowth and guidance processes necessary for the formation of asubset of central and peripheral major fiber tracts. Required forthe development of major fiber tracts in the central nervoussystem, including: the anterior commissure, the corpus callosum,the thalamocortical, corticothalamic and nigrostriatal tracts, thecorticospinal tract, the fasciculus retroflexus, themammillothalamic tract, the medial lemniscus, and ascending fibertracts from the spinal cord to the brain. In the peripheralnervous system, controls axon growth in distinct populations ofcranial and spinal motor neurons, including the facialbranchimotor nerve, the hypoglossal nerve, the phrenic nerve, andmotor nerves innervating dorsal limbs. Involved in the migrationof cranial neural crest cells. May also be implicated in thetransmission of sensory information from the trunk and limbs tothe brain. Controls commissural sensory axons guidance aftermidline crossing along the anterior-posterior axis in thedeveloping spinal cord in a Wnt-dependent signaling pathway.Together with FZD6, is involved in the neural tube closure andplays a role in the regulation of the establishment of planar cellpolarity (PCP), particularly in the orientation of asymmetricbundles of stereocilia on the apical faces of a subset of auditoryand vestibular sensory cells located in the inner ear. Promotesneurogenesis by maintaining sympathetic neuroblasts within thecell cycle in a beta-catenin-dependent manner (By similarity).{ECO:0000250|UniProtKB:Q61086}. Corepressor targeting diverse transcription regulatorssuch as GLIS2 or BCL6. Has dehydrogenase activity. Involved incontrolling the equilibrium between tubular and stacked structuresin the Golgi complex. Functions in brown adipose tissue (BAT)differentiation. {ECO:0000269|PubMed:12419229,ECO:0000269|PubMed:15542832, ECO:0000269|PubMed:18212045,ECO:0000269|PubMed:19103759, ECO:0000269|PubMed:9858600}.

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 FZD3_CTBP1


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 FZD3_CTBP1


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
FZD3SYNE4, VNN2, XAGE1B, UPK1A, GPR21, GPR114, ZBBXCTBP1PNN, IKZF1, SMAD6, RBBP8, TGIF1, NRIP1, MDM2, HDAC1, HDAC3, HDAC4, HDAC5, HDAC9, BRCA1, HDAC2, KAT2B, GEMIN2, TBP, GTF2B, FOXP1, FOXP2, KMT2A, CBX4, MECOM, IKZF4, CTBP2, ZEB1, ACTL6B, HTT, TBL1X, ZNF217, RCOR1, SATB1, CTBP1, TCF4, LCOR, TP53, HIC1, EHMT2, EHMT1, WIZ, APC, PLK1, TUBG1, HSD11B2, TCF7L2, KDM1A, CREBBP, EP300, KAT2A, SP1, RREB1, CDYL, UBE2I, BCORL1, SERPINH1, BCL3, AKT1, HIST3H3, SPEN, ZBP1, SOBP, ZNF219, LCORL, CHD3, RBBP5, CTNNA1, SOX2, ELAVL1, ZEB2, TERF2IP, TERF2, TFAP4, ATXN1L, BCL6, NCOR2, ECT2, CTNNB1, KLF4, DNMT1, RUNX1, BAG3, THAP11, HEMGN, NME2, ORC4, ARNT2, NOL4L, KLF12, MARCH10, CDC23, FUNDC1, IKZF2, KLF3, LNX1, PIAS2, RAI2, RNF111, ZBTB18, CEP68, NOL4, DGCR6, SNRPN, CRY2, HOXB5, PRKAA1, MAPK9, PLCB1, BCAS3, TSHZ3, DMRTB1, EGFR, HIC2, PRDM2, ZNF516, DYRK1A, TRPS1, C10orf12, BCOR, FBXO11, RCOR2, RCOR3, C2orf44, RBL1, INA, RB1, E2F7, TRMT61B, FOXK1, C15orf39, AMPD2, TOR2A, ADSS, ATIC, CARM1, CTH, ECHS1, FKBP1A, GAPDH, DUT, HYI, SSNA1, WDR1, NTRK1, MED23, OFD1, FBF1, KCNIP3, KLF8, NFATC1, NFATC2, MTMR7, RBM14-RBM4, IGFBP1, CHD4, NISCH, KIAA0430, HELZ, PCGF5, SOWAHA, PAN2, EIF4ENIF1, FANCC, FANCA, FANCF, FANCG, FANCL, FANCE, FANCD2, TRIM25


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 FZD3_CTBP1


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 FZD3_CTBP1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFZD3C0036341Schizophrenia5PSYGENET
HgeneFZD3C0033975Psychotic Disorders1PSYGENET
HgeneFZD3C0349204Nonorganic psychosis1PSYGENET
HgeneFZD3C0525045Mood Disorders1PSYGENET
TgeneCTBP1C0009404Colorectal Neoplasms1CTD_human