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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: 23575

FusionGeneSummary for NCDN_TMSB10

check button Fusion gene summary
Fusion gene informationFusion gene name: NCDN_TMSB10
Fusion gene ID: 23575
HgeneTgene
Gene symbol

NCDN

TMSB10

Gene ID

23154

9168

Gene nameneurochondrinthymosin beta 10
Synonyms-MIG12|TB10
Cytomap

1p34.3

2p11.2

Type of geneprotein-codingprotein-coding
Descriptionneurochondrinthymosin beta-10migration-inducing gene 12migration-inducing protein 12
Modification date2018051920180523
UniProtAcc

Q9UBB6

P63313

Ensembl transtripts involved in fusion geneENST00000373253, ENST00000356090, 
ENST00000373243, ENST00000459931, 
ENST00000233143, 
Fusion gene scores* DoF score3 X 3 X 1=99 X 9 X 1=81
# samples 311
** MAII scorelog2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(11/81*10)=0.441509710640035
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: NCDN [Title/Abstract] AND TMSB10 [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
ChiTaRS3.1M79087NCDNchr1

36031945

-TMSB10chr2

85132788

+
* 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
3UTR-5UTRENST00000373253ENST00000233143NCDNchr1

36031945

-TMSB10chr2

85132788

+
3UTR-5UTRENST00000356090ENST00000233143NCDNchr1

36031945

-TMSB10chr2

85132788

+
3UTR-5UTRENST00000373243ENST00000233143NCDNchr1

36031945

-TMSB10chr2

85132788

+
intron-5UTRENST00000459931ENST00000233143NCDNchr1

36031945

-TMSB10chr2

85132788

+

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FusionProtFeatures for NCDN_TMSB10


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

Q9UBB6

TMSB10

P63313

Probably involved in signal transduction, in the nervoussystem, via increasing cell surface localization of GRM5 andpositively regulating its signaling (By similarity). Required forthe spatial learning process. Acts as a negative regulator ofCa(2+)-calmodulin-dependent protein kinase 2 (CaMK2)phosphorylation. May play a role in modulating melanin-concentrating hormone-mediated functions via its interaction withMCHR1 that interferes with G protein-coupled signal transduction.May be involved in bone metabolism. May also be involved inneurite outgrowth. {ECO:0000250, ECO:0000269|PubMed:16945926}. Plays an important role in the organization of thecytoskeleton. Binds to and sequesters actin monomers (G actin) andtherefore inhibits actin polymerization (By similarity).{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 NCDN_TMSB10


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 NCDN_TMSB10


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


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 NCDN_TMSB10


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 NCDN_TMSB10


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneTMSB10C0005586Bipolar Disorder1PSYGENET
TgeneTMSB10C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneTMSB10C0036341Schizophrenia1PSYGENET
TgeneTMSB10C0162820Dermatitis, Allergic Contact1CTD_human