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Fusion Protein:RANBP2-YWHAE |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: RANBP2-YWHAE | FusionPDB ID: 72072 | FusionGDB2.0 ID: 72072 | Hgene | Tgene | Gene symbol | RANBP2 | YWHAE | Gene ID | 5903 | 7531 |
Gene name | RAN binding protein 2 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon | |
Synonyms | ADANE|ANE1|IIAE3|NUP358|TRP1|TRP2 | 14-3-3E|HEL2|KCIP-1|MDCR|MDS | |
Cytomap | 2q13 | 17p13.3 | |
Type of gene | protein-coding | protein-coding | |
Description | E3 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-r | 14-3-3 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 date | 20200313 | 20200327 | |
UniProtAcc | RGPD8 | P62258 | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000283195, | ENST00000498643, ENST00000264335, ENST00000575977, ENST00000571732, ENST00000573026, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 20 X 18 X 8=2880 | 25 X 13 X 12=3900 |
# samples | 21 | 32 | |
** MAII score | log2(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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | RANBP2 | GO:0016925 | protein sumoylation | 17264123|22155184 |
Tgene | YWHAE | GO:0000165 | MAPK cascade | 12917326 |
Tgene | YWHAE | GO:0034605 | cellular response to heat | 12917326 |
Tgene | YWHAE | GO:0046827 | positive regulation of protein export from nucleus | 12917326 |
Tgene | YWHAE | GO:0051480 | regulation of cytosolic calcium ion concentration | 18029012 |
Tgene | YWHAE | GO:0060306 | regulation of membrane repolarization | 11953308 |
Tgene | YWHAE | GO:1901016 | regulation of potassium ion transmembrane transporter activity | 11953308 |
Tgene | YWHAE | GO:1901020 | negative regulation of calcium ion transmembrane transporter activity | 18029012 |
Tgene | YWHAE | GO:1902309 | negative regulation of peptidyl-serine dephosphorylation | 11953308 |
Tgene | YWHAE | GO:1905913 | negative regulation of calcium ion export across plasma membrane | 18029012 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
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![]() * 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. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | STAD | TCGA-CD-A48C-01A | RANBP2 | chr2 | 109336134 | + | YWHAE | chr17 | 1248793 | - |
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Fusion ORF Analysis |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000283195 | RANBP2 | chr2 | 109336134 | + | ENST00000571732 | YWHAE | chr17 | 1248793 | - | 1158 | 198 | 520 | 32 | 162 |
ENST00000283195 | RANBP2 | chr2 | 109336134 | + | ENST00000573026 | YWHAE | chr17 | 1248793 | - | 843 | 198 | 520 | 32 | 162 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000283195 | ENST00000571732 | RANBP2 | chr2 | 109336134 | + | YWHAE | chr17 | 1248793 | - | 0.8812896 | 0.118710354 |
ENST00000283195 | ENST00000573026 | RANBP2 | chr2 | 109336134 | + | YWHAE | chr17 | 1248793 | - | 0.9398217 | 0.060178276 |
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Fusion Amino Acid Sequences |
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>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 |
![]() 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. |
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Hgene | Tgene |
RANBP2 | YWHAE |
1765 | FUNCTION: 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}. |
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- Retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- Not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1171_1307 | 24.0 | 3225.0 | Domain | RanBD1 1 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2012_2148 | 24.0 | 3225.0 | Domain | RanBD1 2 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2309_2445 | 24.0 | 3225.0 | Domain | RanBD1 3 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2911_3046 | 24.0 | 3225.0 | Domain | RanBD1 4 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 3067_3223 | 24.0 | 3225.0 | Domain | PPIase cyclophilin-type |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1001_3206 | 24.0 | 3225.0 | Region | 22 X 2 AA repeats of F-G |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2633_2710 | 24.0 | 3225.0 | Region | Note=Required for E3 SUMO-ligase activity |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2633_2761 | 24.0 | 3225.0 | Region | Note=2 X 50 AA approximate repeats |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1001_1002 | 24.0 | 3225.0 | Repeat | 1 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1101_1102 | 24.0 | 3225.0 | Repeat | 2 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1142_1143 | 24.0 | 3225.0 | Repeat | 3 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1459_1460 | 24.0 | 3225.0 | Repeat | 4 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1523_1524 | 24.0 | 3225.0 | Repeat | 5 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1586_1587 | 24.0 | 3225.0 | Repeat | 6 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 165_201 | 24.0 | 3225.0 | Repeat | TPR 4 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1852_1853 | 24.0 | 3225.0 | Repeat | 7 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1861_1862 | 24.0 | 3225.0 | Repeat | 8 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1900_1901 | 24.0 | 3225.0 | Repeat | 9 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1938_1939 | 24.0 | 3225.0 | Repeat | 10 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1961_1962 | 24.0 | 3225.0 | Repeat | 11 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2260_2261 | 24.0 | 3225.0 | Repeat | 12 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2516_2517 | 24.0 | 3225.0 | Repeat | 13 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2535_2536 | 24.0 | 3225.0 | Repeat | 14 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2545_2546 | 24.0 | 3225.0 | Repeat | 15 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 26_59 | 24.0 | 3225.0 | Repeat | TPR 1 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2711_2761 | 24.0 | 3225.0 | Repeat | 2 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2840_2841 | 24.0 | 3225.0 | Repeat | 16 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2842_2843 | 24.0 | 3225.0 | Repeat | 17 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2863_2864 | 24.0 | 3225.0 | Repeat | 18 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 287_319 | 24.0 | 3225.0 | Repeat | TPR 5 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2880_2881 | 24.0 | 3225.0 | Repeat | 19 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 3106_3107 | 24.0 | 3225.0 | Repeat | 20 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 3189_3190 | 24.0 | 3225.0 | Repeat | 21 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 3205_3206 | 24.0 | 3225.0 | Repeat | 22 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 583_616 | 24.0 | 3225.0 | Repeat | TPR 6 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 60_93 | 24.0 | 3225.0 | Repeat | TPR 2 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 648_681 | 24.0 | 3225.0 | Repeat | TPR 7 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 94_128 | 24.0 | 3225.0 | Repeat | TPR 3 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1351_1381 | 24.0 | 3225.0 | Zinc finger | RanBP2-type 1 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1415_1444 | 24.0 | 3225.0 | Zinc finger | RanBP2-type 2 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1479_1508 | 24.0 | 3225.0 | Zinc finger | RanBP2-type 3 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1543_1572 | 24.0 | 3225.0 | Zinc finger | RanBP2-type 4 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1606_1635 | 24.0 | 3225.0 | Zinc finger | RanBP2-type 5 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1665_1694 | 24.0 | 3225.0 | Zinc finger | RanBP2-type 6 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1724_1753 | 24.0 | 3225.0 | Zinc finger | RanBP2-type 7 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 1781_1810 | 24.0 | 3225.0 | Zinc finger | RanBP2-type 8 |
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Fusion Protein-Protein Interaction |
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Gene | PPI interactors |
RANBP2 | UBE2I, 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, |
YWHAE | IGF1R, 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, |
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Gene | STRING network |
RANBP2 | ![]() |
YWHAE | ![]() |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2147_2287 | 24.0 | 3225.0 | BICD2 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2686_2761 | 24.0 | 3225.0 | SUMO1 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2631_2635 | 24.0 | 3225.0 | sumoylated RANGAP1 |
Hgene | RANBP2 | chr2:109336134 | chr17:1248793 | ENST00000283195 | + | 1 | 29 | 2633_2685 | 24.0 | 3225.0 | UBE2I |
Top |
Related Drugs to RANBP2-YWHAE |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
Top |
Related Diseases to RANBP2-YWHAE |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | RANBP2 | C2675556 | ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 | 3 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Hgene | RANBP2 | C0334121 | Inflammatory Myofibroblastic Tumor | 2 | CTD_human;ORPHANET |
Hgene | RANBP2 | C0018199 | Granuloma, Plasma Cell | 1 | CTD_human |
Hgene | RANBP2 | C4706387 | Acute necrotizing encephalopathy of childhood | 1 | ORPHANET |
Tgene | YWHAE | C0036341 | Schizophrenia | 4 | PSYGENET |
Tgene | YWHAE | C0005586 | Bipolar Disorder | 2 | PSYGENET |
Tgene | YWHAE | C0206630 | Endometrial Stromal Sarcoma | 2 | ORPHANET |
Tgene | YWHAE | C0027627 | Neoplasm Metastasis | 1 | CTD_human |
Tgene | YWHAE | C0265219 | Miller Dieker syndrome | 1 | ORPHANET |
Tgene | YWHAE | C0334488 | Clear cell sarcoma of kidney | 1 | ORPHANET |
Tgene | YWHAE | C2750748 | Chromosome 17p13.3 Duplication Syndrome | 1 | ORPHANET |
Tgene | YWHAE | C4707092 | Distal 17p13.3 microdeletion syndrome | 1 | ORPHANET |