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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: 42409

FusionGeneSummary for YWHAG_OPA3

check button Fusion gene summary
Fusion gene informationFusion gene name: YWHAG_OPA3
Fusion gene ID: 42409
HgeneTgene
Gene symbol

YWHAG

OPA3

Gene ID

7532

80207

Gene nametyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gammaOPA3, outer mitochondrial membrane lipid metabolism regulator
Synonyms14-3-3GAMMA|EIEE56|PPP1R170MGA3
Cytomap

7q11.23

19q13.32

Type of geneprotein-codingprotein-coding
Description14-3-3 protein gammaKCIP-1protein kinase C inhibitor protein 1protein phosphatase 1, regulatory subunit 170tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptideoptic atrophy 3 proteinOptic atrophy 3 (Iraqi-Jewish 'optic atrophy plus')optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
Modification date2018052220180523
UniProtAcc

P61981

Q9H6K4

Ensembl transtripts involved in fusion geneENST00000307630, ENST00000323060, 
ENST00000263275, ENST00000544371, 
Fusion gene scores* DoF score5 X 3 X 3=458 X 7 X 4=224
# samples 59
** MAII scorelog2(5/45*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(9/224*10)=-1.31550182572793
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: YWHAG [Title/Abstract] AND OPA3 [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
TCGARVSKCMTCGA-D9-A149-06AYWHAGchr7

75988039

-OPA3chr19

46057169

-
* 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-intronENST00000307630ENST00000323060YWHAGchr7

75988039

-OPA3chr19

46057169

-
5CDS-intronENST00000307630ENST00000263275YWHAGchr7

75988039

-OPA3chr19

46057169

-
5CDS-5UTRENST00000307630ENST00000544371YWHAGchr7

75988039

-OPA3chr19

46057169

-

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FusionProtFeatures for YWHAG_OPA3


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

P61981

OPA3

Q9H6K4

Adapter protein implicated in the regulation of a largespectrum of both general and specialized signaling pathways. Bindsto a large number of partners, usually by recognition of aphosphoserine or phosphothreonine motif. Binding generally resultsin the modulation of the activity of the binding partner.{ECO:0000269|PubMed:16511572}. May play some role in mitochondrial processes.

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 YWHAG_OPA3


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 YWHAG_OPA3


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
YWHAGKIAA0408, KIF5B, SRRM2, FRYL, MPRIP, PI4KB, KLC1, LARP1, MLLT4, BRAF, EPB41L3, EDC3, OSBPL3, CLASP1, PPFIBP1, KLC4, TJP2, SAMD4B, ERC1, RABGEF1, PRPF4B, IRS2, PARD3, PAK4, MARK2, RAI14, ARAF, CRTC2, SHCBP1, LUC7L2, KRT31, MARK3, KRT85, KIF5C, RAF1, ANKS1A, SNRNP200, KLC3, LBR, RACGAP1, BAIAP2, IGF1R, KIF23, KRT33B, SON, KIAA0930, RMDN3, DENND4A, RABEP1, CGN, MAP3K3, KLC2, GBF1, SFN, HDAC4, KIF1C, FOXO1, PRKCQ, PRKCG, PRKCD, PRKCA, PRKCB, CDK16, DISC1, PRKCZ, MDM4, BAD, EPB41L2, HIVEP2, KRT18, MYH10, PTPN3, SSFA2, TERF1, TNFAIP3, YWHAE, PAK1, FAM65B, CHAF1A, MPHOSPH9, COPS5, SYNPO, NEDD4L, SH3BP4, WWTR1, FAM13B, FAM53C, MSL2, DDX27, CENPJ, CRTC3, WNK1, NDEL1, CGNL1, CEP95, SYNPO2, SIMC1, ANKHD1-EIF4EBP3, HDAC5, ING1, SAMSN1, YWHAQ, ALB, ATP5A1, C1QBP, CDC5L, CLK1, CLK2, CLK3, DHX15, DFFA, DYRK1A, EEF1G, GSK3A, HNRNPH1, HSPA1A, HSPA9, MFAP1, NEFL, CDK17, PIK3C3, PIK3R1, SRSF3, TRA2B, TRIM21, TIAM1, TSC1, UBC, VIM, DDX39B, USP8, ARHGEF2, NOLC1, PPIG, RASAL2, BCLAF1, THRAP3, DCAF7, SRRM1, YAP1, MAP3K2, RNPS1, AKAP13, RASSF8, TUBA3C, PUF60, RAB11FIP2, SAMD4A, MYCBP2, KIF1B, SF3B3, PABPC1, PRPF19, IGKV1-12, CFAP20, TRA2A, ZBTB21, HDAC7, LSR, MIEF1, RALGPS2, MAGOHB, PRPF38B, PRPF40A, NADK, SH3BP5L, MICALL1, FRMD6, SNAP23P, EML3, TMEM102, SRGAP2, LUC7L3, DOCK7, SRSF10, TBC1D1, OPTN, HIST1H3A, EXO1, APP, SS18, YWHAG, APBB1, KAT5, ELAVL1, ARRB1, ARRB2, LATS2, TINF2, POT1, CUL3, CDK2, MEX3B, MAP3K1, LRRK2, AKT1, GRK5, CRK, HNF1A, VCP, FN1, ATF2, GRB2, TRIM32, NOS2, IL7R, ITGA4, ABL1, MST1R, MAPK7, CDC25C, BAG3, ATP6V0B, PLA2G12A, CASP3, LTB4R, HOXC10, SMARCD1, RAB11A, CDK11B, FBXO6, RASSF2, YWHAB, AMOT, PAFAH1B1, PAFAH1B2, PGD, TXNDC5, UBFD1, VCL, ALDH7A1, CAPNS1, CKB, G6PD, GAPDH, GSS, HMGB2, LDHB, PAK2, TGM2, UBE2R2, UBE2V1, YWHAZ, YWHAH, IRS4, DTL, HUWE1, CUL7, CCDC8, TNK1, BTRC, FBXW11, TESPA1, FAM189A2, FRMD5, WWC1, UNK, MCFD2, PABPC4, MCM3, SKP1, NTRK1, LCA5, CEP89, XPO1, CDC25B, KDR, RBM7, WDR62, PPARG, USP37, MCM2, NFATC2, MAP3K5, PPEF2, PPM1H, PTPN4, TENC1, CDC25A, SMTNL2, SPATA13, TFEB, PRICKLE3, PLEKHG5, PAK6, CDCA7, NKD2, ZNF397, DMTN, RIN1, FAM163A, TEX33, SNX24, REEP1, ANKRD55, RAB11FIP1, SSH1, PTPDC1, PTPN14, TSC2, DLD, DLST, SDHA, SOD1, BRD1OPA3APP, KDM1A, PRMT6, SUV39H1, NXF1, NRG1, OPA3, IDE, STOML2, CLPB, ATP5A1, PHYHIPL, YME1L1, SCO2, ECH1, SCO1, TIMM23, C1QBP, ATP5C1, LAMC1, ATP5O, COX5A, STARD7, NRD1, MTCH2, ATP5J, PCDHGB1, TNFRSF17, SLC15A1, PCDHGB4, UBC


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 YWHAG_OPA3


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 YWHAG_OPA3


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneYWHAGC0023893Liver Cirrhosis, Experimental1CTD_human
TgeneOPA3C1833809OPTIC ATROPHY AND CATARACT, AUTOSOMAL DOMINANT1CTD_human;ORPHANET;UNIPROT