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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: 10753

FusionGeneSummary for DYNC1H1_ERBB3

check button Fusion gene summary
Fusion gene informationFusion gene name: DYNC1H1_ERBB3
Fusion gene ID: 10753
HgeneTgene
Gene symbol

DYNC1H1

ERBB3

Gene ID

1778

2065

Gene namedynein cytoplasmic 1 heavy chain 1erb-b2 receptor tyrosine kinase 3
SynonymsCMT2O|DHC1|DHC1a|DNCH1|DNCL|DNECL|DYHC|Dnchc1|HL-3|SMALED1|p22ErbB-3|HER3|LCCS2|MDA-BF-1|c-erbB-3|c-erbB3|erbB3-S|p180-ErbB3|p45-sErbB3|p85-sErbB3
Cytomap

14q32.31

12q13.2

Type of geneprotein-codingprotein-coding
Descriptioncytoplasmic dynein 1 heavy chain 1dynein heavy chain, cytosolicdynein, cytoplasmic, heavy polypeptide 1receptor tyrosine-protein kinase erbB-3human epidermal growth factor receptor 3proto-oncogene-like protein c-ErbB-3tyrosine kinase-type cell surface receptor HER3v-erb-b2 avian erythroblastic leukemia viral oncogene homolog 3
Modification date2018052320180527
UniProtAcc

Q14204

P21860

Ensembl transtripts involved in fusion geneENST00000360184, ENST00000556791, 
ENST00000267101, ENST00000450146, 
ENST00000415288, ENST00000553131, 
ENST00000411731, ENST00000549832, 
Fusion gene scores* DoF score17 X 15 X 7=178525 X 8 X 14=2800
# samples 2025
** MAII scorelog2(20/1785*10)=-3.15785216914174
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(25/2800*10)=-3.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: DYNC1H1 [Title/Abstract] AND ERBB3 [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
TgeneERBB3

GO:0007162

negative regulation of cell adhesion

7556068

TgeneERBB3

GO:0007165

signal transduction

10572067

TgeneERBB3

GO:0009968

negative regulation of signal transduction

11389077

TgeneERBB3

GO:0014065

phosphatidylinositol 3-kinase signaling

7556068

TgeneERBB3

GO:0042127

regulation of cell proliferation

11389077

TgeneERBB3

GO:0051048

negative regulation of secretion

10559227


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
TCGARVHNSCTCGA-UF-A718-01ADYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
* 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-intronENST00000360184ENST00000267101DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
5CDS-intronENST00000360184ENST00000450146DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
5CDS-intronENST00000360184ENST00000415288DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
5CDS-intronENST00000360184ENST00000553131DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
5CDS-intronENST00000360184ENST00000411731DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
5CDS-intronENST00000360184ENST00000549832DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
intron-intronENST00000556791ENST00000267101DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
intron-intronENST00000556791ENST00000450146DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
intron-intronENST00000556791ENST00000415288DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
intron-intronENST00000556791ENST00000553131DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
intron-intronENST00000556791ENST00000411731DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+
intron-intronENST00000556791ENST00000549832DYNC1H1chr14

102517128

+ERBB3chr12

56492035

+

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FusionProtFeatures for DYNC1H1_ERBB3


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
DYNC1H1

Q14204

ERBB3

P21860

Cytoplasmic dynein 1 acts as a motor for theintracellular retrograde motility of vesicles and organelles alongmicrotubules. Dynein has ATPase activity; the force-producingpower stroke is thought to occur on release of ADP. Plays a rolein mitotic spindle assembly and metaphase plate congression(PubMed:27462074). {ECO:0000269|PubMed:27462074}. Tyrosine-protein kinase that plays an essential role ascell surface receptor for neuregulins. Binds to neuregulin-1(NRG1) and is activated by it; ligand-binding increasesphosphorylation on tyrosine residues and promotes its associationwith the p85 subunit of phosphatidylinositol 3-kinase(PubMed:20682778). May also be activated by CSPG5(PubMed:15358134). {ECO:0000269|PubMed:15358134,ECO:0000269|PubMed:20682778}.

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 DYNC1H1_ERBB3


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 DYNC1H1_ERBB3


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
DYNC1H1ARF6, TSC22D1, SNRPB, C20orf24, TOR1A, NME2, DCTN1, NDEL1, PAFAH1B1, BICD2, EPB41, CDC5L, EGFR, RYK, MYC, SPG20, SIRT1, DISC1, TNIK, CSNK2B, ARRB2, SIRT7, CUL3, CDK2, COPS5, KATNA1, KATNB1, LRRK2, GRB2, SNCA, PSEN2, DYNLT1, DYNC1LI2, DYNC1LI1, MAX, SNRPA1, HTATSF1, SRSF9, U2AF2, SF3A1, FUS, DYNLRB1, NCOA5, YARS, STRN, STRN4, XRCC5, FLNC, RANBP9, NUP133, SAP30BP, TNKS1BP1, DYNLT3, LONP1, HNRNPL, TPM2, PLOD3, EPPK1, MCCC1, MCCC2, HEXIM1, ZC3H4, RPA2, LRRFIP1, BRCA1, IKBKAP, HSP90AA1, FN1, VCAM1, PEX14, SMAD2, FAM46A, METTL21A, METTL21C, ITGA4, YWHAQ, AKAP12, DDX1, DYNC1I2, FLNA, PRUNE2, SERBP1, EIF3K, RPS24, RPS5, YBX1, PRKCD, DYNC1I1, SPRTN, TRIM58, HDAC6, RUFY1, CUL7, OBSL1, CCDC8, SUZ12, RNF2, BMI1, USP7, FBXW11, UNK, DCTN2, NCBP1, PIN4, PRMT5, RUVBL2, NTRK1, OFD1, CNTRL, NINL, NIN, NPHP1, RPGRIP1L, SCLT1, POC5, DYNLL1, SYNCRIP, MAPRE1, PPP2R3C, HNRNPD, HSPA1A, MKLN1, CLIP1, TPD52, ACTR1A, RPRD2, GLTSCR1, DCTN4, DCTN5, NUMA1, FOXB1, SKI, CRY2, FOXL1, MCM2, ATOH1, ZNF746, MTNR1B, CYLD, COX15, DLST, DNM1L, HSD17B10, PDHA1, TESERBB3GRB2, PIK3R2, CSK, SHC1, CD82, RGS4, ODF2L, GRB7, PA2G4, EGF, RNF41, NRG1, PIK3R1, IL6ST, PTK6, EGFR, MUC1, NRG2, ERBB2, RPN1, EGR1, ZNF207, HDAC6, LRIG1, MDM2, AKT1, PTPN11, HSP90AA1, NCK2, JAK2, SH2D1A, DAB1, ABL1, HCK, FGFR1, SRC, NCK1, FER, PLCG1, RASA1, TXK, ABL2, ZAP70, SYK, CRK, CRKL, JAK3, VAV2, CHN2, ITK, RIN1, BCAR3, TENC1, TNS3, TNS4, SHC3, PIK3R3, VAV1, VAV3, DAPP1, SH2B3, NEDD4, HLA-DPA1, UQCR10, B3GALTL, PDF, TUBA4A, TUBB8, HLA-A, YBEY, SLC31A1, EIF1AX, SRPK2, HLA-B, SLC25A5, SLC25A6, AIFM1, ANXA2, AP1M2, ATP5A1, B2M, C1QBP, CANX, CDC37, DNAJB11, DNAJA1, TUFM, ERBB3, GFAP, HSPA5, HNRNPH1, HNRNPH2, HNRNPF, HSP90AB1, HSPA8, LGALS3BP, MASP1, PHLDA1, PIK3CA, PIK3CB, PTCD3, RAE1, RPL23, RPS27, RPS27A, RPS27L, MRPS14, MRPS17, MRPS23, MRPS27, MRPS28, S100A10, SSR1, TUBB, ACTA2, ACTB, ACTBL2, POTEKP, ACTC1, ACTG1, ACTG2, ACTA1, HBA1, HBB, HBD, HBE1, HBG1, HBG2, HNRNPH3, HSPA1A, LRPPRC, PON2, POTEE, POTEF, HNRNPA2B1, HNRNPAB, MRPS18B, MRPS22, MRPS25, MRPS26, MRPS34, TUBA1B, PCGF1, DPPA4, NANOG, POU5F1, EPN1, L1CAM, MET, NEDD4L, PTK2B, NDRG1, CDH1, PTPRH, UQCRH, PPM1A, PPM1B, PPM1F, PPM1K, PPM1M, ILKAP, PTPRR, PTPN6, PTPN7, PTPN12, PTPN20B, DUSP14, DUSP18, DUSP19, DUSP21, DUPD1, STYX, PTPDC1, PTEN, TPTE, MTMR1, MTMR2, MTMR6, MTMR8, MTMR9, MTMR10, CDC25C, EYA4, CSPG5, HGS


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 DYNC1H1_ERBB3


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 DYNC1H1_ERBB3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneDYNC1H1C3280220CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O4ORPHANET;UNIPROT
HgeneDYNC1H1C3281202MENTAL RETARDATION, AUTOSOMAL DOMINANT 134UNIPROT
HgeneDYNC1H1C1834690Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant2ORPHANET;UNIPROT
HgeneDYNC1H1C0025958Microcephaly1CTD_human
HgeneDYNC1H1C1955869Malformations of Cortical Development1CTD_human
HgeneDYNC1H1C3714756Intellectual Disability1CTD_human;HPO
TgeneERBB3C0036341Schizophrenia3PSYGENET
TgeneERBB3C0005586Bipolar Disorder1PSYGENET
TgeneERBB3C0011570Mental Depression1PSYGENET
TgeneERBB3C0016978gallbladder neoplasm1CTD_human
TgeneERBB3C0024121Lung Neoplasms1CTD_human
TgeneERBB3C0033578Prostatic Neoplasms1CTD_human
TgeneERBB3C0041696Unipolar Depression1PSYGENET
TgeneERBB3C1269683Major Depressive Disorder1PSYGENET
TgeneERBB3C1458155Mammary Neoplasms1CTD_human
TgeneERBB3C2931822Nasopharyngeal carcinoma1CTD_human