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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:RANBP2-YWHAE

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RANBP2-YWHAE
FusionPDB ID: 72072
FusionGDB2.0 ID: 72072
HgeneTgene
Gene symbol

RANBP2

YWHAE

Gene ID

5903

7531

Gene nameRAN binding protein 2tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon
SynonymsADANE|ANE1|IIAE3|NUP358|TRP1|TRP214-3-3E|HEL2|KCIP-1|MDCR|MDS
Cytomap

2q13

17p13.3

Type of geneprotein-codingprotein-coding
DescriptionE3 SUMO-protein ligase RanBP2358 kDa nucleoporinE3 SUMO-protein transferase RanBP2P270acute necrotizing encephalopathy 1 (autosomal dominant)nuclear pore complex protein Nup358nucleoporin 358nucleoporin Nup358ran-binding protein 2transformation-r14-3-3 protein epsilon14-3-3 epsilonepididymis luminal protein 2mitochondrial import stimulation factor L subunitprotein kinase C inhibitor protein-1tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon polypeptidetyrosine
Modification date2020031320200327
UniProtAcc

RGPD8

P62258

Ensembl transtripts involved in fusion geneENST idsENST00000283195, ENST00000498643, 
ENST00000264335, ENST00000575977, 
ENST00000571732, ENST00000573026, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score20 X 18 X 8=288025 X 13 X 12=3900
# samples 2132
** MAII scorelog2(21/2880*10)=-3.77760757866355
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(32/3900*10)=-3.60733031374961
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: RANBP2 [Title/Abstract] AND YWHAE [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RANBP2(109336134)-YWHAE(1248793), # samples:1
Anticipated loss of major functional domain due to fusion event.RANBP2-YWHAE seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
RANBP2-YWHAE seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
RANBP2-YWHAE seems lost the major protein functional domain in Hgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
RANBP2-YWHAE seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
RANBP2-YWHAE seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
RANBP2-YWHAE seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
RANBP2-YWHAE seems lost the major protein functional domain in Tgene partner, which is a epigenetic factor due to the frame-shifted ORF.
* 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
HgeneRANBP2

GO:0016925

protein sumoylation

17264123|22155184

TgeneYWHAE

GO:0000165

MAPK cascade

12917326

TgeneYWHAE

GO:0034605

cellular response to heat

12917326

TgeneYWHAE

GO:0046827

positive regulation of protein export from nucleus

12917326

TgeneYWHAE

GO:0051480

regulation of cytosolic calcium ion concentration

18029012

TgeneYWHAE

GO:0060306

regulation of membrane repolarization

11953308

TgeneYWHAE

GO:1901016

regulation of potassium ion transmembrane transporter activity

11953308

TgeneYWHAE

GO:1901020

negative regulation of calcium ion transmembrane transporter activity

18029012

TgeneYWHAE

GO:1902309

negative regulation of peptidyl-serine dephosphorylation

11953308

TgeneYWHAE

GO:1905913

negative regulation of calcium ion export across plasma membrane

18029012


check buttonFusion gene breakpoints across RANBP2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across YWHAE (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4STADTCGA-CD-A48C-01ARANBP2chr2

109336134

+YWHAEchr17

1248793

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000283195RANBP2chr2109336134+ENST00000571732YWHAEchr171248793-115819852032162
ENST00000283195RANBP2chr2109336134+ENST00000573026YWHAEchr171248793-84319852032162

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000283195ENST00000571732RANBP2chr2109336134+YWHAEchr171248793-0.88128960.118710354
ENST00000283195ENST00000573026RANBP2chr2109336134+YWHAEchr171248793-0.93982170.060178276

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>72072_72072_1_RANBP2-YWHAE_RANBP2_chr2_109336134_ENST00000283195_YWHAE_chr17_1248793_ENST00000571732_length(amino acids)=162AA_BP=0
MLKKPLCSPVSVLKNLKAGTSKIHRNSLLPLRTFENCLKKKKKNQQGRNLNSETKCKSQIWWFSVTMGSFQRVGWGGGGGQRWFLLLAYV

--------------------------------------------------------------

>72072_72072_2_RANBP2-YWHAE_RANBP2_chr2_109336134_ENST00000283195_YWHAE_chr17_1248793_ENST00000573026_length(amino acids)=162AA_BP=0
MLKKPLCSPVSVLKNLKAGTSKIHRNSLLPLRTFENCLKKKKKNQQGRNLNSETKCKSQIWWFSVTMGSFQRVGWGGGGGQRWFLLLAYV

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr2:109336134/chr17:1248793)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
RANBP2

RGPD8

YWHAE

P62258

1765FUNCTION: Adapter protein implicated in the regulation of a large spectrum of both general and specialized signaling pathways. Binds to a large number of partners, usually by recognition of a phosphoserine or phosphothreonine motif. Binding generally results in the modulation of the activity of the binding partner (By similarity). Positively regulates phosphorylated protein HSF1 nuclear export to the cytoplasm (PubMed:12917326). {ECO:0000250|UniProtKB:P62261, ECO:0000269|PubMed:12917326}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291171_130724.03225.0DomainRanBD1 1
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292012_214824.03225.0DomainRanBD1 2
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292309_244524.03225.0DomainRanBD1 3
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292911_304624.03225.0DomainRanBD1 4
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1293067_322324.03225.0DomainPPIase cyclophilin-type
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291001_320624.03225.0Region22 X 2 AA repeats of F-G
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292633_271024.03225.0RegionNote=Required for E3 SUMO-ligase activity
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292633_276124.03225.0RegionNote=2 X 50 AA approximate repeats
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291001_100224.03225.0Repeat1
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291101_110224.03225.0Repeat2
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291142_114324.03225.0Repeat3
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291459_146024.03225.0Repeat4
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291523_152424.03225.0Repeat5
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291586_158724.03225.0Repeat6
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+129165_20124.03225.0RepeatTPR 4
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291852_185324.03225.0Repeat7
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291861_186224.03225.0Repeat8
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291900_190124.03225.0Repeat9
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291938_193924.03225.0Repeat10
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291961_196224.03225.0Repeat11
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292260_226124.03225.0Repeat12
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292516_251724.03225.0Repeat13
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292535_253624.03225.0Repeat14
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292545_254624.03225.0Repeat15
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+12926_5924.03225.0RepeatTPR 1
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292711_276124.03225.0Repeat2
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292840_284124.03225.0Repeat16
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292842_284324.03225.0Repeat17
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292863_286424.03225.0Repeat18
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+129287_31924.03225.0RepeatTPR 5
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292880_288124.03225.0Repeat19
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1293106_310724.03225.0Repeat20
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1293189_319024.03225.0Repeat21
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1293205_320624.03225.0Repeat22
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+129583_61624.03225.0RepeatTPR 6
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+12960_9324.03225.0RepeatTPR 2
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+129648_68124.03225.0RepeatTPR 7
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+12994_12824.03225.0RepeatTPR 3
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291351_138124.03225.0Zinc fingerRanBP2-type 1
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291415_144424.03225.0Zinc fingerRanBP2-type 2
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291479_150824.03225.0Zinc fingerRanBP2-type 3
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291543_157224.03225.0Zinc fingerRanBP2-type 4
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291606_163524.03225.0Zinc fingerRanBP2-type 5
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291665_169424.03225.0Zinc fingerRanBP2-type 6
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291724_175324.03225.0Zinc fingerRanBP2-type 7
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1291781_181024.03225.0Zinc fingerRanBP2-type 8


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors
RANBP2UBE2I, KPNB1, KPNA1, RAN, Ube2i, OPN1LW, Psmd4, Psmc6, Psmd1, CDC73, AIRE, PARK2, LRPAP1, APC, TAF1, IFT140, AKAP13, FHOD1, ARID4B, CDCA8, HDAC4, tat, RANGAP1, MYC, Plk1, Ranbp2, Kifc5b, CALM1, CEBPA, PSMD1, SIRT7, SENP1, TP53, RAPGEF3, KIFAP3, KIF3A, TOP2B, KIF5B, KIF5C, SP100, NUP214, NUP153, Rangap1, PML, CUL2, NXF1, MATR3, ILF2, EEF1A1, HNRNPK, HNRNPF, HNRNPM, DDX17, SMU1, RRS1, CHMP2A, FLNA, IK, HNRNPH1, DHX15, DHX9, RPS14, TRIM55, PRKDC, M6PR, RRP7A, HSPA1L, ALB, vpu, MMS19, LMNA, ADRB2, BAG3, KPNA2, CUL1, SUMO1, SUMO2, NLK, UBTD1, LGR4, CHFR, CUL7, OBSL1, CCDC8, SUZ12, EED, RNF2, BMI1, RANBP2, NUP62, NUSAP1, COMTD1, SCGN, NUP50, RCC1, ZACN, IER2, FBXW11, CLTC, EFTUD2, IPO5, COL4A3BP, HNRNPC, MED13, PRPF8, PTGES3, RALY, RPLP0, SNRNP200, SRRM1, TOP2A, TUBB, UQCRC2, VCP, KIF3B, NUP43, NUP85, NUP107, NUP133, NUP160, NUP35, NUPL1, SEH1L, Mad2l1, Rcc1, Nup107, Cenpf, Kifc1, Nup155, Nup214, Nup98, FOXB1, CRY2, FOXL1, PRMT5, FOXQ1, WAS, UBA2, MCM2, SNW1, CDC5L, NFATC2, ZNF746, CTDSPL2, PPM1D, B2M, TMEM194A, TRAF3IP3, MDM2, TES, CFTR, MAP2K7, UBE2M, EGLN3, CTNNB1, SLC25A1, BCL2L1, HSPA8, UBE2L6, PIH1D1, TNIP2, RNF4, RNF31, CDC34, ESR2, EZH2, RECQL4, DCPS, WDR76, HIST1H4A, HIST1H2BB, KIAA1429, ATG16L1, RBX1, H2AFX, TPT1, TRADD, NR2C2, GBF1, BICD2, AK3, TNFSF13B, DUSP2, RHBDD1, RHBDF2, BIRC3, LMBR1L, TRIM28, PLEKHA4, MAGEA3, PINK1, FANCD2, PTEN, RALB, EMC1, EMC2, MMGT1, PLBD1, HSPD1, DNAAF3, RAD50, ANKRD55, ESR1, MAU2, MYBPC2, PDLIM3, HSCB, CIT, KIF14, KIF20A, PRC1, NDN, NFX1, RSAD2, NUPR1, C18orf8, CIC, BRD4, LGALS9, KDF1, PCNA, RECQL5, SYNE3, NFKBIA, HTRA4, DDX39A, WDR5, DAXX, NAA40, RGPD1, NPIPB6, PIP, ESRP1, S100A6, BTF3, SLFN11, RCHY1, SIRT6, PLK1, ARRB2,
YWHAEIGF1R, GPRIN2, SORBS2, GRAP2, MAPK7, NDEL1, HDAC4, HDAC5, REM1, BAD, MAP3K10, CDC25C, MAP3K3, MAP3K1, MAP3K2, IRS1, NGFRAP1, SYN2, KCNH2, TNFAIP3, RAF1, CDC25B, TOP2A, TGFB1, CDC25A, Usp8, USP43, POLR3H, HDAC7, MDM4, FOXO3, HIVEP2, LRMP, COX2, MYH10, PNLIP, SSFA2, YWHAB, YWHAZ, YWHAG, ARAF, YWHAH, HDAC9, KIAA0232, TLK1, CHAF1A, CAP2, YWHAQ, RAP1GAP2, SH3BP4, WWTR1, FAM13B, MSL2, ZNF839, RASAL3, WNK1, ENKD1, TBC1D3F, CGNL1, CEP95, ANKHD1-EIF4EBP3, ING1, SRRM2, FAN1, EMD, SAMSN1, EXO1, H2AFX, MYC, PRKAA1, PARD6G, HLA-DRA, HLA-DRB1, HLA-DRB3, HLA-DRB4, HLA-DRB5, DISC1, UBE3A, GAPDH, KAT8, HIST1H3A, HIST1H4A, TCEB3, BRD4, CALM1, FBXO4, CDKN1B, TRAT1, RARRES3, ARRB1, ARRB2, CBL, ACD, POT1, CUL3, CDK2, CUL1, DCUN1D1, NEDD8, PTPN14, MARK3, MARK2, MEX3B, LRRK2, AKT1, ACTA2, CBX3, HNF1A, HSP90AB1, NPM1, ATP5B, ATP5A1, STOML2, CLNS1A, IPO8, KPNB1, RPLP0, RPL6, RPL4, RPS3, RPS8, DNAJA1, EIF4B, EIF3E, EEF1G, EEF1A2, HNRNPA2B1, ILF2, RUVBL2, RCN2, TUBB, TUBB4B, TUBB2B, PRPSAP1, TUBA3E, DDX21, ADH1B, ADH4, AGXT, HIST2H4B, HNRNPA3, HNRNPC, RBMY1A1, SF3B1, PCBP1, RBM10, MAP3K7, TBK1, PPM1B, SPIN1, CDC37, PHB, PRPSAP2, PRPS1, QPCTL, TMPO, C11orf84, HDX, CFAP43, VCP, ATXN1, FN1, VCAM1, BRAF, MAP2K1, PARD3, KIF5B, KLC2, LMO7, TBC1D4, HSPA1A, KLC3, KLC4, KLC1, CLASP2, LIMA1, TSC2, CLASP1, HSPA8, PAK4, RAB11FIP2, MAST3, TBC1D1, KIF1C, OSBPL3, TIAM1, ABLIM1, LARP1, BAIAP2, IRS2, SHROOM2, LSR, KIF1B, RAB11FIP1, MLLT4, MAST2, PFKFB2, CDK18, PKP2, DENND4A, TP53BP2, CGN, ZFP36L2, TUBA1A, KSR1, RABEP1, EIF4E2, CSNK1A1, PDZD11, PRKCI, DCAF7, NADK, USP8, C1QBP, TSC1, REEP1, KIF23, SLC25A6, SRGAP2, FAM53C, TRIP11, BCAR1, CRTC1, RASSF8, CEP250, VAMP8, GRB2, TRIM32, NOS2, IL7R, UBL4A, ITGA4, gag-pol, CBX4, ABL1, MST1R, PAN2, RAD52, BAG3, UL46, GSTA1, FTH1, Wwtr1, Yap1, CDK11B, SRSF1, SRSF6, SRSF4, NOLC1, TRA2B, PLEKHO2, HMHA1, SRSF7, NCBP1, DOK3, VASP, KIAA0930, GAB2, KIAA0226, PIK3R4, SGK223, RCHY1, IGHG1, UVRAG, SRSF2, FBXO6, RASSF2, SAV1, YAP1, PARK2, PAFAH1B2, PPP1R2, PROSC, RAP1GDS1, TMOD3, TNFAIP8, TUBB2A, UBXN1, VCL, XPO1, ALDH7A1, ASNS, ATIC, CAPN2, CAPNS1, EIF5, FERMT2, G6PD, GSS, ISOC1, MCTS1, STK26, OGFOD1, PAK2, PDHB, PDIA4, PTMA, SCPEP1, TBCB, TWF2, UBE2R2, IRS4, SIK3, SIK2, CEP57, TP53, GRB10, DTL, HUWE1, FBXW11, Mdm4, CUL7, OBSL1, CCDC8, MAST1, CDK16, TNK1, BTRC, NKD2, DMTN, TEX33, Numb, EPB41L3, WWC1, HNRNPA1, HSPB1, UNK, ACAT2, CALR, CENPE, MACF1, MAPK14, MCFD2, POLR2D, PSMB2, SHMT2, SNRPD1, ACTR6, HNRNPL, NPM3, PGK1, PSMC1, ZPR1, NTRK1, LCA5, CENPJ, PRICKLE3, MYH11, TSNAX, CCDC88A, CRY1, CRY2, MCM2, Ksr1, CDC5L, ERRFI1, U2AF2, PRDX6, NFATC2, SNF8, ANKZF1, SMAGP, TCEANC, LCP2, METAP2, MAGEB4, CHST11, ZC3HC1, MCM10, DDX54, C8orf59, NAF1, FGF12, GSTM3, STAC, FAM64A, ATP6V0B, FLJ25758, CDC73, WWP2, CDH1, CEP131, PCM1, PPM1H, PTPN3, SSH1, TENC1, SMTNL2, PLEKHG5, SAMD4A, SPATA13, RIN1, TFEB, TESPA1, SAMD4B, FAM163A, CRTC2, FAM189A2, PAK6, RBM3, RAB3IP, CBY1, CEP170, INPP5E, SLC9A1, CYLD, COX15, DLD, DLST, DNM1L, SDHA, SOAT1, VDAC1, TRIM25, BRCA1, BRD1, BRMS1, YLR177W, ACM1, IFNAR1, CFTR, TARDBP, ZNF598, CTNNB1, MEX3C, EGLN3, RIPK4, PTPN4, API5, KRAS, PPP6C, COPE, GRHPR, JUP, PPIE, YAF2, PARD3B, RPA2, NIN, AKAP9, CASK, PRC1, RBM14, UBE2M, RAD18, EFTUD2, AAR2, PIH1D1, TNIP2, RNF31, HAVCR1, BPLF1, ESR2, HEXIM1, MEPCE, PPT1, AGR2, EZH2, RECQL4, KANK1, STUB1, BAP1, PIK3R1, GPC1, Prkaa1, Nav2, KIAA1429, RC3H1, RC3H2, ATG16L1, ACTC1, FAF1, CLIC4, FHL1, FHL2, FHL3, LMO1, LMO2, LMO3, TET2, KCTD15, GBF1, AGRN, BMH1, BMH2, ATXN3, HIBADH, DIABLO, NDUFAB1, ALDH1B1, ALDH2, COQ9, FH, HEXA, HSP90AA1, LDHB, MMP20, RAD23A, TIMM44, UBA1, VBP1, AARS2, ECH1, GRPEL1, IARS2, PAFAH2, PFDN4, SSBP1, DYRK1A, MAPT, CD74, SLC15A3, GEM, DUSP16, MTMR4, PTPDC1, ITFG1, BIRC3, NFX1, nsp7ab, ORF3a, CCDC125, PLEKHA4, PINK1, FANCD2, NGB, ZC3H18, CSK, PDPK1, PRKCE, PRKD1, SHC1, SHOC2, SFN, PHACTR4, MAP3K5, CHAF1B, CAMSAP3, LRCH1, SH2B3, CDK12, TANC2, EPN3, PANK2, MAP3K15, CEP89, FRMD6, THAP11, TTC17, CCNY, ARHGEF19, FAM122B, DAB2IP, FAM110C, LPIN1, PRR5, DNMT1, CDK11A, SRSF10, TBC1D7, NEDD4L, FAM117B, KANK2, DENND4C, RGS12, YWHAE, EMC4, ERC2, APPL2, ANKRD55, ESR1, SNAPIN, EDC3, NEK4, CHMP4C, CCR9, CYSLTR2, RXFP3, KIF14, RMDN3, HNRNPH1, INS, Rnf183, NUPR1, CIC, CCAR2, Apc2, RBM39, LGALS9, ACTN4, BTF3, CAD, CALD1, CDKN2A, COPA, DDB1, DDX6, DHX9, EIF2B1, GOLGA3, HDAC1, JAK1, LTBP1, PPP1R12A, NONO, PA2G4, PAWR, PRPS2, RBBP4, ROCK1, SMARCC2, TRIM21, TAF4, EIF3A, PABPC4, LRRFIP2, MTA2, VPRBP, EIF4A3, MATR3, HDAC6, SAE1, G3BP1, SMC2, IVNS1ABP, SF3B2, FASTKD2, NT5C2, STK38L, MGA, UBR2, CAND1, EFHD2, SHCBP1, SFPQ, TAB3, TAB1, ACAP2, INSIG1, NEDD4, SOD1, IL1B, UFL1, DDRGK1, KRT8, VAPA, FZR1, PAGE4, NUDCD2, LNP1, SNX33, FAM53B, SYNGAP1, CDR2L, GUCA1B, KIAA1211, ARHGEF4, FAM124A, EPB41L1, AFAP1L1, MIIP, PLEKHA3, GAREM, CD28, GPSM3, SIPA1L3, PDE7B, C19orf26, C6orf222, PSD4, MACC1, ZNF395, FAM86C1, SH2D3A, NCKIPSD, KSR2, SPRTN, TRIM26, FBXW7, FGD5, CCNF, HECTD1, NBR1, SQSTM1, MAP1LC3B, SLFN11, RIPK2, PER2,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
RANBP2all structure
YWHAEall structure


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292147_228724.03225.0BICD2
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292686_276124.03225.0SUMO1
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292631_263524.03225.0sumoylated RANGAP1
HgeneRANBP2chr2:109336134chr17:1248793ENST00000283195+1292633_268524.03225.0UBE2I


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Related Drugs to RANBP2-YWHAE


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to RANBP2-YWHAE


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneRANBP2C2675556ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 33CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
HgeneRANBP2C0334121Inflammatory Myofibroblastic Tumor2CTD_human;ORPHANET
HgeneRANBP2C0018199Granuloma, Plasma Cell1CTD_human
HgeneRANBP2C4706387Acute necrotizing encephalopathy of childhood1ORPHANET
TgeneYWHAEC0036341Schizophrenia4PSYGENET
TgeneYWHAEC0005586Bipolar Disorder2PSYGENET
TgeneYWHAEC0206630Endometrial Stromal Sarcoma2ORPHANET
TgeneYWHAEC0027627Neoplasm Metastasis1CTD_human
TgeneYWHAEC0265219Miller Dieker syndrome1ORPHANET
TgeneYWHAEC0334488Clear cell sarcoma of kidney1ORPHANET
TgeneYWHAEC2750748Chromosome 17p13.3 Duplication Syndrome1ORPHANET
TgeneYWHAEC4707092Distal 17p13.3 microdeletion syndrome1ORPHANET