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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: 20832

FusionGeneSummary for MAP3K10_C19orf47

check button Fusion gene summary
Fusion gene informationFusion gene name: MAP3K10_C19orf47
Fusion gene ID: 20832
HgeneTgene
Gene symbol

MAP3K10

C19orf47

Gene ID

4294

126526

Gene namemitogen-activated protein kinase kinase kinase 10chromosome 19 open reading frame 47
SynonymsMEKK10|MLK2|MST-
Cytomap

19q13.2

19q13.2

Type of geneprotein-codingprotein-coding
Descriptionmitogen-activated protein kinase kinase kinase 10MKN28 derived nonreceptor_type serine/threonine kinaseMKN28 kinasemixed lineage kinase 2protein kinase MSTuncharacterized protein C19orf47
Modification date2018052320180519
UniProtAcc

Q02779

Q8N9M1

Ensembl transtripts involved in fusion geneENST00000253055, ENST00000593906, 
ENST00000582783, ENST00000392035, 
ENST00000584868, 
Fusion gene scores* DoF score4 X 4 X 4=643 X 2 X 2=12
# samples 43
** MAII scorelog2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MAP3K10 [Title/Abstract] AND C19orf47 [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
HgeneMAP3K10

GO:0018105

peptidyl-serine phosphorylation

19801649

HgeneMAP3K10

GO:0018107

peptidyl-threonine phosphorylation

19801649


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
TCGARVLUSCTCGA-85-A510-01AMAP3K10chr19

40715126

+C19orf47chr19

40847797

-
* 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
Frame-shiftENST00000253055ENST00000582783MAP3K10chr19

40715126

+C19orf47chr19

40847797

-
5CDS-5UTRENST00000253055ENST00000392035MAP3K10chr19

40715126

+C19orf47chr19

40847797

-
5CDS-intronENST00000253055ENST00000584868MAP3K10chr19

40715126

+C19orf47chr19

40847797

-
intron-3CDSENST00000593906ENST00000582783MAP3K10chr19

40715126

+C19orf47chr19

40847797

-
intron-5UTRENST00000593906ENST00000392035MAP3K10chr19

40715126

+C19orf47chr19

40847797

-
intron-intronENST00000593906ENST00000584868MAP3K10chr19

40715126

+C19orf47chr19

40847797

-

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FusionProtFeatures for MAP3K10_C19orf47


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MAP3K10

Q02779

C19orf47

Q8N9M1

Activates the JUN N-terminal pathway. {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 MAP3K10_C19orf47


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 MAP3K10_C19orf47


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
MAP3K10NEUROD1, CDC42, RAC1, KIF17, KIF3A, KIFAP3, YWHAE, HPCA, HTT, MAPK8IP1, MAPK8IP2, DNM1, CLTC, DLG4, HGS, ABL2, KIAA1804, COPS2, MAPK9, MAP3K10, MAPK1, MAPK14, GARS, MAP2K4, SMURF1C19orf47PRKAA2, NTM, CCDC8, MORF4L1, LRP8, THOC5, EMC2, THOC1, RNASEH2A, C17orf85, THOC2, THOC7


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 MAP3K10_C19orf47


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 MAP3K10_C19orf47


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