FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 23118

FusionGeneSummary for MYO19_SSH2

check button Fusion gene summary
Fusion gene informationFusion gene name: MYO19_SSH2
Fusion gene ID: 23118
HgeneTgene
Gene symbol

MYO19

SSH2

Gene ID

80179

85464

Gene namemyosin XIXslingshot protein phosphatase 2
SynonymsMYOHD1SSH-2|SSH-2L
Cytomap

17q12

17q11.2

Type of geneprotein-codingprotein-coding
Descriptionunconventional myosin-XIXmyosin head domain containing 1myosin head domain-containing protein 1protein phosphatase Slingshot homolog 2SSH-like protein 2
Modification date2018051920180523
UniProtAcc

Q96H55

Q76I76

Ensembl transtripts involved in fusion geneENST00000431794, ENST00000268852, 
ENST00000586007, ENST00000544606, 
ENST00000590081, 
ENST00000269033, 
ENST00000540801, ENST00000324677, 
ENST00000582084, ENST00000590153, 
ENST00000579954, 
Fusion gene scores* DoF score5 X 5 X 5=12515 X 11 X 8=1320
# samples 615
** MAII scorelog2(6/125*10)=-1.05889368905357
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(15/1320*10)=-3.13750352374993
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MYO19 [Title/Abstract] AND SSH2 [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
HgeneMYO19

GO:0034642

mitochondrion migration along actin filament

19932026


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
TCGARVUCECTCGA-BK-A26L-01CMYO19chr17

34881059

-SSH2chr17

28120955

-
* 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-shiftENST00000431794ENST00000269033MYO19chr17

34881059

-SSH2chr17

28120955

-
Frame-shiftENST00000431794ENST00000540801MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000431794ENST00000324677MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000431794ENST00000582084MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000431794ENST00000590153MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000431794ENST00000579954MYO19chr17

34881059

-SSH2chr17

28120955

-
Frame-shiftENST00000268852ENST00000269033MYO19chr17

34881059

-SSH2chr17

28120955

-
Frame-shiftENST00000268852ENST00000540801MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000268852ENST00000324677MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000268852ENST00000582084MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000268852ENST00000590153MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000268852ENST00000579954MYO19chr17

34881059

-SSH2chr17

28120955

-
Frame-shiftENST00000586007ENST00000269033MYO19chr17

34881059

-SSH2chr17

28120955

-
Frame-shiftENST00000586007ENST00000540801MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000586007ENST00000324677MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000586007ENST00000582084MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000586007ENST00000590153MYO19chr17

34881059

-SSH2chr17

28120955

-
5CDS-intronENST00000586007ENST00000579954MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-3CDSENST00000544606ENST00000269033MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-3CDSENST00000544606ENST00000540801MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-intronENST00000544606ENST00000324677MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-intronENST00000544606ENST00000582084MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-intronENST00000544606ENST00000590153MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-intronENST00000544606ENST00000579954MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-3CDSENST00000590081ENST00000269033MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-3CDSENST00000590081ENST00000540801MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-intronENST00000590081ENST00000324677MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-intronENST00000590081ENST00000582084MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-intronENST00000590081ENST00000590153MYO19chr17

34881059

-SSH2chr17

28120955

-
intron-intronENST00000590081ENST00000579954MYO19chr17

34881059

-SSH2chr17

28120955

-

Top

FusionProtFeatures for MYO19_SSH2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MYO19

Q96H55

SSH2

Q76I76

Actin-based motor molecule with ATPase activity thatlocalizes to the mitochondrion outer membrane (PubMed:19932026,PubMed:23568824, PubMed:25447992). Motor protein that movestowards the plus-end of actin filaments (By similarity). Requiredfor mitochondrial inheritance during mitosis (PubMed:25447992).May be involved in mitochondrial transport or positioning(PubMed:23568824). {ECO:0000250|UniProtKB:Q5SV80,ECO:0000269|PubMed:19932026, ECO:0000269|PubMed:25447992,ECO:0000305|PubMed:23568824}. Protein phosphatase which regulates actin filamentdynamics. Dephosphorylates and activates the actinbinding/depolymerizing factor cofilin, which subsequently binds toactin filaments and stimulates their disassembly. Inhibitoryphosphorylation of cofilin is mediated by LIMK1, which may also bedephosphorylated and inactivated by this protein.{ECO:0000269|PubMed:11832213}.

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


Top

FusionGeneSequence for MYO19_SSH2


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).

Top

FusionGenePPI for MYO19_SSH2


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
MYO19MYL10, HLA-DQA1, HLA-DPA1, NRG1, ACTG1, ACTN4, ACTN1, ADD3, AP2A1, AP2B1, ANXA2, CALD1, CAPZA1, CAPZA2, CAPZB, CCT6A, CD44, CFL1, CFL2, AP2M1, CLTA, CLTB, CLTC, CPM, MAPK14, DAB2, DAPK3, DBN1, DCTN1, DSG2, CTTN, STOM, EPS15, FLII, FLNA, FLNB, FLOT2, GART, GNAI1, GNB2, GSN, HSP90AB1, ITGB4, ITPR3, ABLIM1, LMO7, MYO1B, MSN, MYH9, MYH10, MYL6, MYLK, MYO1C, MYO1E, MYO5A, MYO5B, MYO6, MYO10, PPP1R12A, PPP1R12B, NAP1L1, PIK3C2A, PLEC, PPP1CA, PPP1CC, TWF1, SIPA1, SPTAN1, SPTBN1, SPTBN2, SSFA2, ST5, SVIL, TJP1, TMOD1, TPM1, TPM2, TPM3, TPM4, VDAC1, VDAC2, CORO2A, LUZP1, CLTCL1, PICALM, IQGAP1, HIP1R, GPRC5A, LRRFIP2, TJP2, CLINT1, ARHGAP11A, SEC16A, WDR1, TOM1, ARPC4, ARPC3, ARPC1B, ACTR3, ACTR2, ARPC2, FLOT1, TUBA1B, BASP1, DCTN2, CCT4, MYL12A, GAS2L1, IMMT, SYNPO, LIMCH1, PALLD, SIPA1L3, MPRIP, COBL, SPECC1L, FBXO46, CORO1C, PLEKHG3, SIPA1L1, RAI14, ZBTB20, TMOD3, CARD10, LIMA1, GTSE1, CHCHD3, BMP2K, PPP1R9A, ACTR10, UNC45A, ERBB2IP, MYO5C, CDC42SE2, CORO1B, KIAA1211, MICAL3, ARHGAP21, ENOPH1, AFAP1, INF2, AHNAK, CYBRD1, PPP1CB, ANLN, MYO18A, ARPC5L, L3MBTL2, ANTXR1, PPP1R9B, STON2, DOCK7, SSH2, RHOT2, PHLDB2, NEXN, MYADM, SPECC1, FCHO2, MISP, CHMP4B, MYL6B, KRT72, ARHGAP42, PPP1R18, TTC9C, GAS2L3, PTRF, TPRN, MYL2, IL13RA2, CD79B, PHKG2, RAC1, TRIM25SSH2ACTB, ELAVL1, BAG3, XPO1, CAPZA2, DBN1, FLNA, MYH9, PPP1CB, IQGAP1, KIF3A, SYNPO, LIMA1, ANLN, MYO19, MYO18A, GAN, FBXW7, MYO1D, 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


Top

RelatedDrugs for MYO19_SSH2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

RelatedDiseases for MYO19_SSH2


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