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Fusion gene ID: 39298 |
FusionGeneSummary for TRA2A_HECW1 |
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Fusion gene information | Fusion gene name: TRA2A_HECW1 | Fusion gene ID: 39298 | Hgene | Tgene | Gene symbol | TRA2A | HECW1 | Gene ID | 29896 | 23072 |
Gene name | transformer 2 alpha homolog | HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1 | |
Synonyms | AWMS1|HSU53209 | NEDL1 | |
Cytomap | 7p15.3 | 7p14.1-p13 | |
Type of gene | protein-coding | protein-coding | |
Description | transformer-2 protein homolog alphaTRA-2 alphaTRA2-alphaTra2alphahtra-2 alphaputative MAPK activating protein PM24transformer-2 alphatransformer-2 protein homolog A | E3 ubiquitin-protein ligase HECW1HECT type E3 ubiquitin ligaseHECT-type E3 ubiquitin transferase HECW1NEDD4-like ubiquitin-protein ligase 1 | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | Q13595 | Q76N89 | |
Ensembl transtripts involved in fusion gene | ENST00000297071, ENST00000392502, ENST00000538367, ENST00000474586, | ENST00000395891, ENST00000453890, ENST00000471043, | |
Fusion gene scores | * DoF score | 8 X 7 X 5=280 | 5 X 5 X 4=100 |
# samples | 10 | 5 | |
** MAII score | log2(10/280*10)=-1.48542682717024 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(5/100*10)=-1 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: TRA2A [Title/Abstract] AND HECW1 [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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | TRA2A | GO:0000398 | mRNA splicing, via spliceosome | 9546399 |
![]() (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 type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | LD | BRCA | TCGA-EW-A3U0-01A | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
Frame-shift | ENST00000297071 | ENST00000395891 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
Frame-shift | ENST00000297071 | ENST00000453890 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
5CDS-intron | ENST00000297071 | ENST00000471043 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
5UTR-3CDS | ENST00000392502 | ENST00000395891 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
5UTR-3CDS | ENST00000392502 | ENST00000453890 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
5UTR-intron | ENST00000392502 | ENST00000471043 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
5UTR-3CDS | ENST00000538367 | ENST00000395891 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
5UTR-3CDS | ENST00000538367 | ENST00000453890 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
5UTR-intron | ENST00000538367 | ENST00000471043 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
5UTR-3CDS | ENST00000474586 | ENST00000395891 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
5UTR-3CDS | ENST00000474586 | ENST00000453890 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
5UTR-intron | ENST00000474586 | ENST00000471043 | TRA2A | chr7 | 23561326 | - | HECW1 | chr7 | 43351362 | + |
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FusionProtFeatures for TRA2A_HECW1 |
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Hgene | Tgene |
TRA2A | HECW1 |
Sequence-specific RNA-binding protein which participatesin the control of pre-mRNA splicing. {ECO:0000269|PubMed:9546399}. | E3 ubiquitin-protein ligase that mediates ubiquitinationand subsequent degradation of DVL1. Also targets the mutant SOD1protein involved in familial amyotrophic lateral sclerosis (FALS).Forms cytotoxic aggregates with DVL1, SSR3 and mutant SOD1 thatlead to motor neuron death in FALS. {ECO:0000269|PubMed:14684739}. |
![]() * 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. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and 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 |
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FusionGeneSequence for TRA2A_HECW1 |
![]() (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 TRA2A_HECW1 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
TRA2A | TADA2A, YWHAG, NUDT21, SELENBP1, CRABP1, TNNT1, CDK2AP2, C11orf58, ELAVL1, CUL3, CUL5, COPS5, SRSF10, RBM25, SRSF5, CDC5L, SEPT2, NFIA, NHP2L1, NCSTN, SF3A1, BUD31, SF3B3, PHGDH, S100A9, HNRNPC, HNRNPU, PRPF40A, SF3B6, HNRNPM, SAP18, PRPF6, IK, HP1BP3, SEPT7, SMARCB1, PLEC, BARD1, PAXIP1, MAGOH, EIF4A3, PPP1CC, DHX15, U2SURP, CDK6, LBP, NXF1, YTHDC1, CLK3, SRPK2, OBSL1, EZH2, SUZ12, EED, RNF2, BMI1, ZNF22, LARP7, SRRM1, MRPS9, MRPS26, THRAP3, LUC7L2, LUC7L, ZNF768, PTCD1, PTCD3, SRRM2, C17orf85, ZFR, PABPC4L, PABPC4, RBBP6, ELAVL2, RPL6, MRPS23, MRPS27, TRUB2, MRPS6, RPL26L1, MTERF3, PAIP1, MRPS18B, MRPL32, C10orf2, MRPS10, DAP3, MEPCE, UPF1, PPIG, LARP1, LARP1B, PHAX, MRPS31, MKRN1, MRPS18C, MRPS5, MRPS7, MRPS22, MRPS15, MRPS35, MRPS25, RRP9, NGRN, MRPS2, MOV10, MRPS33, SRRT, PRPF3, MRPS11, PNN, SRP14, GAR1, MRPS24, CASC3, WDR33, CSNK1E, CSNK1D, MRPS14, GAPDHS, ZCCHC3, MKRN2, ZC3H11A, NOA1, TRA2B, ISY1, SRSF8, CLK1, SRSF7, APOBEC3F, HIST1H2AG, SRSF12, CLK2, MRPL34, MRPS21, SNIP1, NTRK1, SRSF3, SRSF6, EWSR1, CNTRL, CDK2, FEN1, U2AF2, SNRNP70, ZC3H18, C11orf57, SNRPN, NCOA5, PABPC1, SYF2, APOBEC3D, NR3C1, FOXA1 | HECW1 | DVL1, SSR4, SOD1, SCNN1A, SCNN1B, TNK2, CACNA1A, TP53, RNF43, GFI1B, USP7, FBXL15, HECW2, LDLRAD4, MPHOSPH8, UBC, UBE2D1, UBE2D2, UBE2D3, UBE2L3, HECW1, UBE2J2, FAM189B |
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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 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for TRA2A_HECW1 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for TRA2A_HECW1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | TRA2A | C0037274 | Dermatologic disorders | 1 | CTD_human |
Hgene | TRA2A | C0311375 | Arsenic Poisoning | 1 | CTD_human |