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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: 42387

FusionGeneSummary for YWHAB_GLO1

check button Fusion gene summary
Fusion gene informationFusion gene name: YWHAB_GLO1
Fusion gene ID: 42387
HgeneTgene
Gene symbol

YWHAB

GLO1

Gene ID

7529

2739

Gene nametyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein betaglyoxalase I
SynonymsGW128|HEL-S-1|HS1|KCIP-1|YWHAAGLOD1|GLYI|HEL-S-74
Cytomap

20q13.12

6p21.2

Type of geneprotein-codingprotein-coding
Description14-3-3 protein beta/alpha14-3-3 alphabrain protein 14-3-3, beta isoformepididymis secretory protein Li 1protein 1054protein kinase C inhibitor protein-1tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, alpha polypeptidetyrosinlactoylglutathione lyaseS-D-lactoylglutathione methylglyoxal lyasealdoketomutaseepididymis secretory protein Li 74glx Iglyoxalase domain containing 1ketone-aldehyde mutaselactoyl glutathione lyasemethylglyoxalase
Modification date2018052220180527
UniProtAcc

P31946

Q04760

Ensembl transtripts involved in fusion geneENST00000353703, ENST00000479421, 
ENST00000372839, 
ENST00000373365, 
ENST00000470973, 
Fusion gene scores* DoF score9 X 9 X 5=4053 X 3 X 3=27
# samples 154
** MAII scorelog2(15/405*10)=-1.43295940727611
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/27*10)=0.567040592723894
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: YWHAB [Title/Abstract] AND GLO1 [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
HgeneYWHAB

GO:0035308

negative regulation of protein dephosphorylation

17255105

HgeneYWHAB

GO:0043085

positive regulation of catalytic activity

17255105

HgeneYWHAB

GO:0051220

cytoplasmic sequestering of protein

10869435

TgeneGLO1

GO:0043066

negative regulation of apoptotic process

11489834


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
TCGARVCOADTCGA-DM-A1D7-01AYWHABchr20

43514527

+GLO1chr6

38654750

-
* 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
5UTR-3CDSENST00000353703ENST00000373365YWHABchr20

43514527

+GLO1chr6

38654750

-
5UTR-intronENST00000353703ENST00000470973YWHABchr20

43514527

+GLO1chr6

38654750

-
3UTR-3CDSENST00000479421ENST00000373365YWHABchr20

43514527

+GLO1chr6

38654750

-
3UTR-intronENST00000479421ENST00000470973YWHABchr20

43514527

+GLO1chr6

38654750

-
5UTR-3CDSENST00000372839ENST00000373365YWHABchr20

43514527

+GLO1chr6

38654750

-
5UTR-intronENST00000372839ENST00000470973YWHABchr20

43514527

+GLO1chr6

38654750

-

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FusionProtFeatures for YWHAB_GLO1


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

P31946

GLO1

Q04760

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. Negativeregulator of osteogenesis. Blocks the nuclear translocation of thephosphorylated form (by AKT1) of SRPK2 and antagonizes itsstimulatory effect on cyclin D1 expression resulting in blockageof neuronal apoptosis elicited by SRPK2. Negative regulator ofsignaling cascades that mediate activation of MAP kinases viaAKAP13. {ECO:0000269|PubMed:17717073, ECO:0000269|PubMed:19592491,ECO:0000269|PubMed:21224381}. Catalyzes the conversion of hemimercaptal, formed frommethylglyoxal and glutathione, to S-lactoylglutathione. Involvedin the regulation of TNF-induced transcriptional activity of NF-kappa-B. Required for normal osteoclastogenesis.{ECO:0000269|PubMed:19199007, ECO:0000269|PubMed:23122816,ECO:0000269|PubMed:9705294}.

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 YWHAB_GLO1


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 YWHAB_GLO1


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
YWHABKIF5B, MPRIP, SRRM2, IRS2, RAI14, SAMD4B, BRAF, PI4KB, USP8, EPB41L3, PARD3, KLC1, MLLT4, RACGAP1, KIF23, EDC3, TJP2, FOXK1, DENND4A, FRYL, SLC4A7, MARK3, NCKAP1, AKAP13, OSBPL3, CGN, RMDN3, RABGEF1, LARP1, CSNK2A1, RASGRF1, MAPK7, RAF1, RPS6KA1, HDAC4, HDAC5, WEE1, BAD, PTPN3, ZFP36, IGF1R, RGS3, CBL, KCNK3, TESK1, TESK2, IRS1, PRKCZ, PRPF6, MLXIP, TNFAIP3, CDC25B, LYST, ITGB1, MAPT, CDC25A, UCP2, UCP3, USP43, USP32, WDR20, MDM4, FOXO3, CDC25C, TSC2, TSC1, YWHAE, ING1, CAMK2A, CAMK2B, EMD, SAMSN1, HDAC7, EXO1, CHAF1A, H2AFX, MYC, NEDD4L, YWHAQ, SKP2, ATP5A1, C1QBP, DHX15, HSPA1B, HSPA5, HSP90AB1, SRSF3, SON, UBC, DOCK4, PIK3R2, MAP3K2, SRSF10, RNPS1, STK38, TUBA3C, STK38L, MYCBP2, KIAA0930, GAPVD1, PIK3R4, LSR, RALGPS2, ALS2, WDR77, RIOK1, MICALL1, FRMD6, CRTC2, TUBB, MAP2K1, MAP2K2, RFWD2, OPTN, HES1, CDKN1B, HIST1H3A, ELAVL1, ARRB1, ARRB2, CUL3, DCUN1D1, ITGB2, PTPN14, MEX3B, MARK2, LRRK2, KIF13B, GRK5, APP, ACTA2, ATG4B, ECT2, HNF1A, VCP, FN1, VCAM1, ZFP36L1, ATF2, IQCB1, GRB2, TRIM32, ITGA4, CBX4, ABL1, PHB, BAX, MST1R, KCNK9, KCNJ11, GPR15, BAG3, BCL2L11, CDK11B, SRPK2, KLC2, RASSF2, YAP1, ABLIM1, AGAP3, AKT1S1, AMPD2, ANKS1A, ARAF, ARHGEF2, CEP131, BAIAP2, VIPAS39, CAMKK1, CCDC6, CDC42EP1, CDK16, CDK17, CDK18, CEP170, CLASP1, CLASP2, NELFB, CRTC3, CYFIP2, CYLD, DCAF7, DDX6, DENND1A, DENND4C, DOCK11, EIF4E2, DMTN, FAM83B, GBF1, GIGYF1, GIGYF2, GRIP1, HGS, INPP5F, IRS4, CEP170B, KIAA0355, KIAA1671, KIAA1804, KIF1B, KIF1C, KLC4, KSR1, LIMA1, LMO7, LUZP1, MARK1, MAST2, MTMR12, NADK, NAV1, NCKIPSD, NF1, PAK4, PARP8, PFKFB2, PHLDB2, PIK3C2A, PKP2, PLEKHA5, PLEKHA7, PPFIA1, PPFIBP1, PPM1H, PPP2R5D, PTPN13, PUM1, R3HDM1, R3HDM2, RAB11FIP1, RAB11FIP2, RAPGEF6, RASAL2, REEP4, RICTOR, RTKN, SAMD4A, SH3PXD2A, SH3RF1, SH3RF3, SHKBP1, SHROOM3, SIPA1L2, SIPA1L3, SKIV2L2, SORBS1, SORBS2, SRGAP2, STAM, STK3, TANC2, TBC1D1, TBC1D22A, TBC1D22B, TBC1D4, TBC1D5, TP53BP2, TPD52L1, TTC28, UHRF1BP1L, USP54, VPS33B, WDR62, NELFA, WNK1, YWHAG, YWHAH, YWHAZ, ZAK, ZCCHC8, ZFP36L2, CAPZA1, PAFAH1B2, PAK2, PGD, SLC9A3R1, SMS, BCCIP, DAK, G6PD, GSS, LDHB, RRAGB, SGTA, TUBB4B, SIK3, DDIT4, DTL, CUL7, RNF115, EGFR, MAST1, TNK1, BTRC, FBXW11, FRMD5, WWC1, HSPB1, UNK, NCAPD3, PITHD1, SLK, NTRK1, HIST1H2BG, LCA5, CHORDC1, CENPJ, PPARG, CRY1, MCM2, DACT1, NFATC2, ERRFI1, CDC73, CDH1, DUSP16, MTMR4, SMTNL2, SPATA13, PRICKLE3, TESPA1, SFN, FAM189A2, NKD2, STAC, TFEB, FAM163A, PTPDC1, PTPN4, SSH1, MTNR1A, MTNR1B, DLD, DNM1L, PARK7, SDHA, SOAT1, SOD1, FOXA1, TRIM25, G3BP1, URI1, BRD1, TP53GLO1CPLX1, IGBP1, PNP, AGL, ITPA, IKBKG, MAP3K13, ASB12, MEOX2, CUL7, ACY1, AKR1B1, AKR1B15, ATIC, FABP5, ALDOA, ALDOC, GMPS, HSPB1, PGAM1, PRDX6, PREP, UMPS, GLOD4, GRHPR, HNRNPA1, HSD17B14, HSPE1, IMPA2, PGM3, PGP, PPA1, PSMG4, QDPR, STIP1, TKT, EWSR1, FOS, CDC25C, EYA4, SOD1, 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


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RelatedDrugs for YWHAB_GLO1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneGLO1Q04760DB00328IndomethacinLactoylglutathione lyasesmall moleculeapproved|investigational
TgeneGLO1Q04760DB00143GlutathioneLactoylglutathione lyasesmall moleculeapproved|investigational|nutraceutical

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RelatedDiseases for YWHAB_GLO1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneGLO1C0011570Mental Depression2PSYGENET
TgeneGLO1C0011581Depressive disorder2CTD_human;PSYGENET
TgeneGLO1C0003469Anxiety Disorders1CTD_human
TgeneGLO1C0004352Autistic Disorder1CTD_human
TgeneGLO1C0005586Bipolar Disorder1PSYGENET
TgeneGLO1C0025202melanoma1CTD_human
TgeneGLO1C0036341Schizophrenia1PSYGENET
TgeneGLO1C0279626Squamous cell carcinoma of esophagus1CTD_human