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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:RAF1-EIF3L

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: RAF1-EIF3L
FusionPDB ID: 71821
FusionGDB2.0 ID: 71821
HgeneTgene
Gene symbol

RAF1

EIF3L

Gene ID

6037

51386

Gene nameribonuclease A family member 3eukaryotic translation initiation factor 3 subunit L
SynonymsECP|RAF1|RNS3EIF3EIP|EIF3S11|EIF3S6IP|HSPC021|HSPC025|MSTP005
Cytomap

14q11.2

22q13.1

Type of geneprotein-codingprotein-coding
Descriptioneosinophil cationic proteinRNase 3cytotoxic ribonucleaseribonuclease 3ribonuclease, RNase A family, 3eukaryotic translation initiation factor 3 subunit LeIEF associated protein HSPC021eukaryotic translation initiation factor 3 subunit 6-interacting proteineukaryotic translation initiation factor 3 subunit E-interacting protein
Modification date2020031320200322
UniProtAcc

P04049

Q9Y262

Ensembl transtripts involved in fusion geneENST idsENST00000251849, ENST00000442415, 
ENST00000542177, ENST00000534997, 
ENST00000476955, ENST00000381683, 
ENST00000406934, ENST00000412331, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score24 X 15 X 16=576010 X 13 X 6=780
# samples 2813
** MAII scorelog2(28/5760*10)=-4.36257007938471
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(13/780*10)=-2.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: RAF1 [Title/Abstract] AND EIF3L [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)RAF1(12653449)-EIF3L(38282772), # samples:1
RAF1(12660013)-EIF3L(38282771), # samples:1
Anticipated loss of major functional domain due to fusion event.RAF1-EIF3L 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.
RAF1-EIF3L 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.
RAF1-EIF3L seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
RAF1-EIF3L seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
RAF1-EIF3L seems lost the major protein functional domain in Hgene partner, which is a kinase due to the frame-shifted ORF.
RAF1-EIF3L seems lost the major protein functional domain in Tgene partner, which is a essential gene 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
HgeneRAF1

GO:0002227

innate immune response in mucosa

12860195

HgeneRAF1

GO:0019731

antibacterial humoral response

12860195

HgeneRAF1

GO:0043152

induction of bacterial agglutination

23992292

HgeneRAF1

GO:0045087

innate immune response

23992292

HgeneRAF1

GO:0050829

defense response to Gram-negative bacterium

23992292

HgeneRAF1

GO:0050830

defense response to Gram-positive bacterium

12860195|23992292

HgeneRAF1

GO:0061844

antimicrobial humoral immune response mediated by antimicrobial peptide

12860195

TgeneEIF3L

GO:0006413

translational initiation

17581632

TgeneEIF3L

GO:0075525

viral translational termination-reinitiation

21347434


check buttonFusion gene breakpoints across RAF1 (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 EIF3L (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
ChimerDB4DLBCTCGA-G8-6325-01ARAF1chr3

12653449

-EIF3Lchr22

38282772

+
ChimerDB4DLBCTCGA-G8-6325RAF1chr3

12660013

-EIF3Lchr22

38282771

+


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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)
ENST00000251849RAF1chr312653449-ENST00000412331EIF3Lchr2238282772+182376010361425129
ENST00000251849RAF1chr312653449-ENST00000381683EIF3Lchr2238282772+895760440766108
ENST00000251849RAF1chr312653449-ENST00000406934EIF3Lchr2238282772+1046760440766108
ENST00000442415RAF1chr312653449-ENST00000412331EIF3Lchr2238282772+17456829581347129
ENST00000442415RAF1chr312653449-ENST00000381683EIF3Lchr2238282772+817682362688108
ENST00000442415RAF1chr312653449-ENST00000406934EIF3Lchr2238282772+968682362688108
ENST00000542177RAF1chr312660013-ENST00000412331EIF3Lchr2238282771+16015388141203129
ENST00000542177RAF1chr312660013-ENST00000381683EIF3Lchr2238282771+673538331657108
ENST00000542177RAF1chr312660013-ENST00000406934EIF3Lchr2238282771+824538331657108

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
ENST00000251849ENST00000412331RAF1chr312653449-EIF3Lchr2238282772+0.1117206960.8882793
ENST00000251849ENST00000381683RAF1chr312653449-EIF3Lchr2238282772+0.084902090.9150979
ENST00000251849ENST00000406934RAF1chr312653449-EIF3Lchr2238282772+0.108614280.8913857
ENST00000442415ENST00000412331RAF1chr312653449-EIF3Lchr2238282772+0.116843190.8831568
ENST00000442415ENST00000381683RAF1chr312653449-EIF3Lchr2238282772+0.1231462960.8768537
ENST00000442415ENST00000406934RAF1chr312653449-EIF3Lchr2238282772+0.1488660.851134
ENST00000542177ENST00000412331RAF1chr312660013-EIF3Lchr2238282771+0.0425645260.9574354
ENST00000542177ENST00000381683RAF1chr312660013-EIF3Lchr2238282771+0.049131190.9508688
ENST00000542177ENST00000406934RAF1chr312660013-EIF3Lchr2238282771+0.057606380.94239366

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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

>71821_71821_1_RAF1-EIF3L_RAF1_chr3_12653449_ENST00000251849_EIF3L_chr22_38282772_ENST00000381683_length(amino acids)=108AA_BP=
MEHIQGAWKTISNGFGFKDAVFDGSSCISPTIVQQFGYQRRASDDGKLTDPSKTSNTIRVFLPNKQRTVVNVRNGMSLHDCLMKALKVRG

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

>71821_71821_2_RAF1-EIF3L_RAF1_chr3_12653449_ENST00000251849_EIF3L_chr22_38282772_ENST00000406934_length(amino acids)=108AA_BP=
MEHIQGAWKTISNGFGFKDAVFDGSSCISPTIVQQFGYQRRASDDGKLTDPSKTSNTIRVFLPNKQRTVVNVRNGMSLHDCLMKALKVRG

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

>71821_71821_3_RAF1-EIF3L_RAF1_chr3_12653449_ENST00000251849_EIF3L_chr22_38282772_ENST00000412331_length(amino acids)=129AA_BP=41
MEPDLSSHYCRREFVGCGSNTFPMCPDAFRIHQLLVFKLSYFYFVLLRWSLTLSPRLECSSVISVRCILRCPGSSSSASAFQVAGITGVC

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

>71821_71821_4_RAF1-EIF3L_RAF1_chr3_12653449_ENST00000442415_EIF3L_chr22_38282772_ENST00000381683_length(amino acids)=108AA_BP=
MEHIQGAWKTISNGFGFKDAVFDGSSCISPTIVQQFGYQRRASDDGKLTDPSKTSNTIRVFLPNKQRTVVNVRNGMSLHDCLMKALKVRG

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

>71821_71821_5_RAF1-EIF3L_RAF1_chr3_12653449_ENST00000442415_EIF3L_chr22_38282772_ENST00000406934_length(amino acids)=108AA_BP=
MEHIQGAWKTISNGFGFKDAVFDGSSCISPTIVQQFGYQRRASDDGKLTDPSKTSNTIRVFLPNKQRTVVNVRNGMSLHDCLMKALKVRG

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

>71821_71821_6_RAF1-EIF3L_RAF1_chr3_12653449_ENST00000442415_EIF3L_chr22_38282772_ENST00000412331_length(amino acids)=129AA_BP=41
MEPDLSSHYCRREFVGCGSNTFPMCPDAFRIHQLLVFKLSYFYFVLLRWSLTLSPRLECSSVISVRCILRCPGSSSSASAFQVAGITGVC

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

>71821_71821_7_RAF1-EIF3L_RAF1_chr3_12660013_ENST00000542177_EIF3L_chr22_38282771_ENST00000381683_length(amino acids)=108AA_BP=69
MEHIQGAWKTISNGFGFKDAVFDGSSCISPTIVQQFGYQRRASDDGKLTDPSKTSNTIRVFLPNKQRTVDMIHIADTKVARRYGDFFIRQ

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

>71821_71821_8_RAF1-EIF3L_RAF1_chr3_12660013_ENST00000542177_EIF3L_chr22_38282771_ENST00000406934_length(amino acids)=108AA_BP=69
MEHIQGAWKTISNGFGFKDAVFDGSSCISPTIVQQFGYQRRASDDGKLTDPSKTSNTIRVFLPNKQRTVDMIHIADTKVARRYGDFFIRQ

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

>71821_71821_9_RAF1-EIF3L_RAF1_chr3_12660013_ENST00000542177_EIF3L_chr22_38282771_ENST00000412331_length(amino acids)=129AA_BP=41
MEPDLSSHYCRREFVGCGSNTFPMCPDAFRIHQLLVFKLSYFYFVLLRWSLTLSPRLECSSVISVRCILRCPGSSSSASAFQVAGITGVC

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

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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/chr3:12653449/chr22:38282772)
- 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
RAF1

P04049

EIF3L

Q9Y262

FUNCTION: Serine/threonine-protein kinase that acts as a regulatory link between the membrane-associated Ras GTPases and the MAPK/ERK cascade, and this critical regulatory link functions as a switch determining cell fate decisions including proliferation, differentiation, apoptosis, survival and oncogenic transformation. RAF1 activation initiates a mitogen-activated protein kinase (MAPK) cascade that comprises a sequential phosphorylation of the dual-specific MAPK kinases (MAP2K1/MEK1 and MAP2K2/MEK2) and the extracellular signal-regulated kinases (MAPK3/ERK1 and MAPK1/ERK2). The phosphorylated form of RAF1 (on residues Ser-338 and Ser-339, by PAK1) phosphorylates BAD/Bcl2-antagonist of cell death at 'Ser-75'. Phosphorylates adenylyl cyclases: ADCY2, ADCY5 and ADCY6, resulting in their activation. Phosphorylates PPP1R12A resulting in inhibition of the phosphatase activity. Phosphorylates TNNT2/cardiac muscle troponin T. Can promote NF-kB activation and inhibit signal transducers involved in motility (ROCK2), apoptosis (MAP3K5/ASK1 and STK3/MST2), proliferation and angiogenesis (RB1). Can protect cells from apoptosis also by translocating to the mitochondria where it binds BCL2 and displaces BAD/Bcl2-antagonist of cell death. Regulates Rho signaling and migration, and is required for normal wound healing. Plays a role in the oncogenic transformation of epithelial cells via repression of the TJ protein, occludin (OCLN) by inducing the up-regulation of a transcriptional repressor SNAI2/SLUG, which induces down-regulation of OCLN. Restricts caspase activation in response to selected stimuli, notably Fas stimulation, pathogen-mediated macrophage apoptosis, and erythroid differentiation. {ECO:0000269|PubMed:11427728, ECO:0000269|PubMed:11719507, ECO:0000269|PubMed:15385642, ECO:0000269|PubMed:15618521, ECO:0000269|PubMed:15849194, ECO:0000269|PubMed:16892053, ECO:0000269|PubMed:16924233, ECO:0000269|PubMed:9360956}.FUNCTION: Component of the eukaryotic translation initiation factor 3 (eIF-3) complex, which is required for several steps in the initiation of protein synthesis (PubMed:17581632, PubMed:25849773, PubMed:27462815). The eIF-3 complex associates with the 40S ribosome and facilitates the recruitment of eIF-1, eIF-1A, eIF-2:GTP:methionyl-tRNAi and eIF-5 to form the 43S pre-initiation complex (43S PIC). The eIF-3 complex stimulates mRNA recruitment to the 43S PIC and scanning of the mRNA for AUG recognition. The eIF-3 complex is also required for disassembly and recycling of post-termination ribosomal complexes and subsequently prevents premature joining of the 40S and 60S ribosomal subunits prior to initiation (PubMed:17581632). The eIF-3 complex specifically targets and initiates translation of a subset of mRNAs involved in cell proliferation, including cell cycling, differentiation and apoptosis, and uses different modes of RNA stem-loop binding to exert either translational activation or repression (PubMed:25849773). {ECO:0000255|HAMAP-Rule:MF_03011, ECO:0000269|PubMed:17581632, ECO:0000269|PubMed:25849773, ECO:0000269|PubMed:27462815}.; FUNCTION: (Microbial infection) In case of FCV infection, plays a role in the ribosomal termination-reinitiation event leading to the translation of VP2 (PubMed:18056426). {ECO:0000269|PubMed:18056426}.

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
HgeneRAF1chr3:12653449chr22:38282772ENST00000251849-317349_609106.66666666666667649.0DomainProtein kinase
HgeneRAF1chr3:12653449chr22:38282772ENST00000251849-31756_131106.66666666666667649.0DomainRBD
HgeneRAF1chr3:12653449chr22:38282772ENST00000442415-318349_609106.66666666666667669.0DomainProtein kinase
HgeneRAF1chr3:12653449chr22:38282772ENST00000442415-31856_131106.66666666666667669.0DomainRBD
HgeneRAF1chr3:12660013chr22:38282771ENST00000251849-217349_60969.0649.0DomainProtein kinase
HgeneRAF1chr3:12660013chr22:38282771ENST00000251849-21756_13169.0649.0DomainRBD
HgeneRAF1chr3:12660013chr22:38282771ENST00000442415-218349_60969.0669.0DomainProtein kinase
HgeneRAF1chr3:12660013chr22:38282771ENST00000442415-21856_13169.0669.0DomainRBD
HgeneRAF1chr3:12653449chr22:38282772ENST00000251849-317355_363106.66666666666667649.0Nucleotide bindingATP
HgeneRAF1chr3:12653449chr22:38282772ENST00000442415-318355_363106.66666666666667669.0Nucleotide bindingATP
HgeneRAF1chr3:12660013chr22:38282771ENST00000251849-217355_36369.0649.0Nucleotide bindingATP
HgeneRAF1chr3:12660013chr22:38282771ENST00000442415-218355_36369.0669.0Nucleotide bindingATP
HgeneRAF1chr3:12653449chr22:38282772ENST00000251849-317138_184106.66666666666667649.0Zinc fingerPhorbol-ester/DAG-type
HgeneRAF1chr3:12653449chr22:38282772ENST00000442415-318138_184106.66666666666667669.0Zinc fingerPhorbol-ester/DAG-type
HgeneRAF1chr3:12660013chr22:38282771ENST00000251849-217138_18469.0649.0Zinc fingerPhorbol-ester/DAG-type
HgeneRAF1chr3:12660013chr22:38282771ENST00000442415-218138_18469.0669.0Zinc fingerPhorbol-ester/DAG-type
TgeneEIF3Lchr3:12653449chr22:38282772ENST00000381683811331_537477.0517.0DomainPCI
TgeneEIF3Lchr3:12653449chr22:38282772ENST000004123311013331_537525.0565.0DomainPCI
TgeneEIF3Lchr3:12660013chr22:38282771ENST00000381683811331_537477.0517.0DomainPCI
TgeneEIF3Lchr3:12660013chr22:38282771ENST000004123311013331_537525.0565.0DomainPCI


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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
RAF1YWHAQ, YWHAG, YWHAZ, Hras, SFN, HRAS, VDAC1, PEBP4, CNKSR1, RASD2, CNKSR2, ERAS, SPRY4, SPRY2, YWHAB, OIP5, PHKA2, CCT3, MYC, AR, MRAS, KRAS, LRPAP1, RRAS2, SHOC2, TSC22D3, STK26, MAPK1, MAPK3, PRKCE, BCL2, BCL2L1, PEBP1, MAP2K1, GRB10, NRAS, MAPK8IP3, AKT1, HSP90AA1, GNG4, GNB2, VAV1, RHEB, RAP1A, SRC, FYN, RB1, RBL2, PRKG1, JAK2, YWHAH, CFLAR, CDC25A, BRAF, MAP3K1, PDGFRB, MAP3K5, MAPK7, PHB, BAG1, PAK1, PRKCZ, RRAS, PRPF6, UBE2D2, YWHAE, NR3C1, LCK, LTK, JAK1, XIAP, BIRC2, BIRC3, STUB1, Arrb2, EEF1A1, HSP82, HSPA8, HSPA5, CALM1, SGK1, NEDD4, SCNN1B, NEDD4L, STK3, BRAP, WDR83, KSR1, LATS1, MAP2K2, Rfxank, RFXANK, PPP1CC, VCP, HSPD1, BAD, BCL6, BIRC7, PIN1, MMS19, PPP2R1A, PPP2R2B, PPP2CA, HSPA4, RAF1, PPP2CB, MAPK8, RBBP8, YY1, PKM, CDK20, HIPK4, TBXA2R, SH3KBP1, ILK, GPRASP2, CDC37, IRS4, FAM96B, HUWE1, Prkab1, RANBP9, TMEM70, PACSIN3, NPLOC4, PRKAR1A, DCAF8, PURA, FYCO1, MYBPC1, COPS7A, MOV10, NXF1, EGFR, CALU, CCT8, DNAJA1, EMD, TIMM50, LOX, ARRB2, AGTR1, CASZ1, MRC2, PDLIM2, HERC2, XPO1, ACOX1, PCDH7, MAD2L1, SYNPO, TMEM63B, EEF1E1, COPS5, SS18L2, Smn1, Cep152, Aldh4a1, Ksr1, NUP133, RPGRIP1L, NCAPG2, NUP107, MSH2, LAS1L, AMER1, NUP160, EIF3D, SPATA7, NPHP4, DYNLL2, DYNLL1, IQCB1, RMDN3, TRIM25, Mapkbp1, EGLN3, RIPK4, MAPK6, CSNK1A1, HERC1, LZTR1, QKI, COPS3, TRIM28, MAEA, NANOG, ITCH, IRF7, PSMB9, MAP2K5, CDK4, CDK6, CDKN2B, FGFR4, MAP2K3, NF2, PDGFRA, TEAD2, RASSF1, ABCB5, BECN1, CBLC, GLIS2, GRM1, HGF, MAP2K6, ARNT, CCND2, CD44, CDKN2A, CDKN2C, EPHA2, ERBB2, KEAP1, LATS2, MET, NF1, TERT, DUSP2, MBP, PAK2, PLEKHA4, CRBN, ARAF, SLC25A3, TUBB4B, TUBB, HSPA6, HSP90AB3P, HSP90AB1, HSPA1A, HSPB1, BAG2, CCT7, DSG1, CCT2, CCT4, CCT6A, TCP1, AKAP8L, ATAD3A, ABCD3, SLC25A22, TMEM33, TUBA4A, HPX, MGST1, TUBB4A, TMEM161A, HSP90AB2P, CCAR2, SLC25A10, FANCD2, TUBB6, HSD17B12, SLC25A11, SLC25A1, ARL1, DNAJA2, DPM1, CCT5, AIFM1, SQSTM1, TUBG2, TUBG1, STK39, GCN1L1, ABCF2, POLD1, NUBP2, TM9SF3, NCLN, SEC61A2, SEC61A1, ALDH1A3, TUBB3, POLR2B, IARS2, TMED1, CIT, AURKB, KIF20A, BRD1, TRIM66, HAX1, CUL4A, ACTR1A, AKAP1, FLOT1, LAMTOR1, LMAN1, RAB2A, RAB4A, STX7, NPAS1, OPALIN, METTL21B, SSSCA1, FAM174A, CRKL, DDB1, DICER1, LDHB, PIK3R1, NONO, DVL2,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
RAF1all structure
EIF3L


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
HgeneRAF1chr3:12653449chr22:38282772ENST00000251849-317331_349106.66666666666667649.0PEBP1/RKIP
HgeneRAF1chr3:12653449chr22:38282772ENST00000442415-318331_349106.66666666666667669.0PEBP1/RKIP
HgeneRAF1chr3:12660013chr22:38282771ENST00000251849-217331_34969.0649.0PEBP1/RKIP
HgeneRAF1chr3:12660013chr22:38282771ENST00000442415-218331_34969.0669.0PEBP1/RKIP


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Related Drugs to RAF1-EIF3L


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 RAF1-EIF3L


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
HgeneRAF1C0028326Noonan Syndrome10CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneRAF1C0175704LEOPARD Syndrome7CLINGEN;CTD_human;GENOMICS_ENGLAND
HgeneRAF1C1969057Noonan Syndrome 54CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneRAF1C1969056LEOPARD SYNDROME 23CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneRAF1C0007194Hypertrophic Cardiomyopathy2CTD_human
HgeneRAF1C0041409Turner Syndrome, Male2CTD_human
HgeneRAF1C1519086Pilomyxoid astrocytoma2ORPHANET
HgeneRAF1C1527404Female Pseudo-Turner Syndrome2CTD_human
HgeneRAF1C4551472Hypertrophic obstructive cardiomyopathy2CTD_human
HgeneRAF1C4551602Noonan Syndrome 12CTD_human
HgeneRAF1C0006142Malignant neoplasm of breast1CTD_human
HgeneRAF1C0007131Non-Small Cell Lung Carcinoma1CTD_human
HgeneRAF1C0007193Cardiomyopathy, Dilated1CTD_human
HgeneRAF1C0017638Glioma1CTD_human
HgeneRAF1C0020429Hyperalgesia1CTD_human
HgeneRAF1C0022665Kidney Neoplasm1CTD_human
HgeneRAF1C0023903Liver neoplasms1CTD_human
HgeneRAF1C0024121Lung Neoplasms1CTD_human
HgeneRAF1C0242379Malignant neoplasm of lung1CTD_human
HgeneRAF1C0259783mixed gliomas1CTD_human
HgeneRAF1C0340427Familial dilated cardiomyopathy1ORPHANET
HgeneRAF1C0345904Malignant neoplasm of liver1CTD_human
HgeneRAF1C0345967Malignant mesothelioma1CTD_human
HgeneRAF1C0458247Allodynia1CTD_human
HgeneRAF1C0555198Malignant Glioma1CTD_human
HgeneRAF1C0587248Costello syndrome (disorder)1CLINGEN
HgeneRAF1C0678222Breast Carcinoma1CTD_human
HgeneRAF1C0740457Malignant neoplasm of kidney1CTD_human
HgeneRAF1C0751211Hyperalgesia, Primary1CTD_human
HgeneRAF1C0751212Hyperalgesia, Secondary1CTD_human
HgeneRAF1C0751213Tactile Allodynia1CTD_human
HgeneRAF1C0751214Hyperalgesia, Thermal1CTD_human
HgeneRAF1C1257931Mammary Neoplasms, Human1CTD_human
HgeneRAF1C1275081Cardio-facio-cutaneous syndrome1CLINGEN
HgeneRAF1C1449563Cardiomyopathy, Familial Idiopathic1CTD_human
HgeneRAF1C1458155Mammary Neoplasms1CTD_human
HgeneRAF1C2936719Mechanical Allodynia1CTD_human
HgeneRAF1C4014656CARDIOMYOPATHY, DILATED, 1NN1CTD_human;UNIPROT
HgeneRAF1C4551484Leopard Syndrome 11CTD_human;GENOMICS_ENGLAND
HgeneRAF1C4704874Mammary Carcinoma, Human1CTD_human
HgeneRAF1C4721610Carcinoma, Ovarian Epithelial1CTD_human