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Fusion Protein:MSRB3-HMGA2 |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: MSRB3-HMGA2 | FusionPDB ID: 55426 | FusionGDB2.0 ID: 55426 | Hgene | Tgene | Gene symbol | MSRB3 | HMGA2 | Gene ID | 253827 | 8091 |
Gene name | methionine sulfoxide reductase B3 | high mobility group AT-hook 2 | |
Synonyms | DFNB74 | BABL|HMGI-C|HMGIC|LIPO|STQTL9 | |
Cytomap | 12q14.3 | 12q14.3 | |
Type of gene | protein-coding | protein-coding | |
Description | methionine-R-sulfoxide reductase B3methionine-R-sulfoxide reductase B3, mitochondrial | high mobility group protein HMGI-CHMGA2/KRT121P fusionhigh-mobility group (nonhistone chromosomal) protein isoform I-C | |
Modification date | 20200313 | 20200329 | |
UniProtAcc | Q8IXL7 | P52926 | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000308259, ENST00000355192, ENST00000535664, ENST00000540804, ENST00000538725, | ENST00000354636, ENST00000393578, ENST00000425208, ENST00000536545, ENST00000393577, ENST00000403681, ENST00000541363, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 7 X 5 X 4=140 | 16 X 12 X 5=960 |
# samples | 7 | 15 | |
** MAII score | log2(7/140*10)=-1 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(15/960*10)=-2.67807190511264 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: MSRB3 [Title/Abstract] AND HMGA2 [Title/Abstract] AND fusion [Title/Abstract] Fusion of the HMGA2 and C9orf92 genes in myolipoma with t(9;12)(p22;q14) (pmid: 26857357) | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | HMGA2(66232349)-MSRB3(65856934), # samples:2 HMGA2(66232349)-MSRB3(65856935), # samples:2 MSRB3(65762806)-HMGA2(66345162), # samples:1 MSRB3(65762806)-HMGA2(66345163), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | HMGA2-MSRB3 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. HMGA2-MSRB3 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. MSRB3-HMGA2 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. MSRB3-HMGA2 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. MSRB3-HMGA2 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. MSRB3-HMGA2 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. HMGA2-MSRB3 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF. HMGA2-MSRB3 seems lost the major protein functional domain in Hgene partner, which is a transcription factor due to the frame-shifted ORF. HMGA2-MSRB3 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF. MSRB3-HMGA2 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF. MSRB3-HMGA2 seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF. MSRB3-HMGA2 seems lost the major protein functional domain in Tgene partner, which is a transcription 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 | MSRB3 | GO:0030091 | protein repair | 14699060 |
Tgene | HMGA2 | GO:0000122 | negative regulation of transcription by RNA polymerase II | 14627817 |
Tgene | HMGA2 | GO:0002062 | chondrocyte differentiation | 21484705 |
Tgene | HMGA2 | GO:0006284 | base-excision repair | 19465398 |
Tgene | HMGA2 | GO:0007095 | mitotic G2 DNA damage checkpoint | 16061642 |
Tgene | HMGA2 | GO:0010564 | regulation of cell cycle process | 14645522 |
Tgene | HMGA2 | GO:0010628 | positive regulation of gene expression | 18832382 |
Tgene | HMGA2 | GO:0031052 | chromosome breakage | 19549901 |
Tgene | HMGA2 | GO:0031507 | heterochromatin assembly | 16901784 |
Tgene | HMGA2 | GO:0035978 | histone H2A-S139 phosphorylation | 16061642 |
Tgene | HMGA2 | GO:0035986 | senescence-associated heterochromatin focus assembly | 16901784 |
Tgene | HMGA2 | GO:0035988 | chondrocyte proliferation | 21484705 |
Tgene | HMGA2 | GO:0042769 | DNA damage response, detection of DNA damage | 19465398 |
Tgene | HMGA2 | GO:0043065 | positive regulation of apoptotic process | 16061642 |
Tgene | HMGA2 | GO:0043066 | negative regulation of apoptotic process | 19465398 |
Tgene | HMGA2 | GO:0043392 | negative regulation of DNA binding | 14645522 |
Tgene | HMGA2 | GO:0043922 | negative regulation by host of viral transcription | 17005673 |
Tgene | HMGA2 | GO:0045869 | negative regulation of single stranded viral RNA replication via double stranded DNA intermediate | 17005673 |
Tgene | HMGA2 | GO:0045892 | negative regulation of transcription, DNA-templated | 18832382 |
Tgene | HMGA2 | GO:0045893 | positive regulation of transcription, DNA-templated | 15225648|15755872|17005673|17324944|17426251 |
Tgene | HMGA2 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 14645522|18832382 |
Tgene | HMGA2 | GO:0071158 | positive regulation of cell cycle arrest | 16061642 |
Tgene | HMGA2 | GO:0071902 | positive regulation of protein serine/threonine kinase activity | 19549901 |
Tgene | HMGA2 | GO:0090402 | oncogene-induced cell senescence | 16901784 |
Tgene | HMGA2 | GO:2000648 | positive regulation of stem cell proliferation | 21484705 |
Tgene | HMGA2 | GO:2000679 | positive regulation of transcription regulatory region DNA binding | 18832382 |
Tgene | HMGA2 | GO:2000685 | positive regulation of cellular response to X-ray | 16061642 |
Tgene | HMGA2 | GO:2001022 | positive regulation of response to DNA damage stimulus | 16061642|19465398 |
Tgene | HMGA2 | GO:2001033 | negative regulation of double-strand break repair via nonhomologous end joining | 19549901 |
Tgene | HMGA2 | GO:2001038 | regulation of cellular response to drug | 16061642 |
![]() * 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 | SARC | TCGA-DX-A7EI-01A | MSRB3 | chr12 | 65762806 | + | HMGA2 | chr12 | 66345163 | + |
ChimerDB4 | SARC | TCGA-DX-A7EI | MSRB3 | chr12 | 65762806 | + | HMGA2 | chr12 | 66345162 | + |
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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) |
ENST00000355192 | MSRB3 | chr12 | 65762806 | + | ENST00000541363 | HMGA2 | chr12 | 66345162 | + | 7911 | 439 | 111 | 482 | 123 |
ENST00000308259 | MSRB3 | chr12 | 65762806 | + | ENST00000541363 | HMGA2 | chr12 | 66345162 | + | 8038 | 566 | 226 | 609 | 127 |
ENST00000540804 | MSRB3 | chr12 | 65762806 | + | ENST00000541363 | HMGA2 | chr12 | 66345162 | + | 7822 | 350 | 22 | 393 | 123 |
ENST00000535664 | MSRB3 | chr12 | 65762806 | + | ENST00000541363 | HMGA2 | chr12 | 66345162 | + | 8103 | 631 | 291 | 674 | 127 |
ENST00000355192 | MSRB3 | chr12 | 65762806 | + | ENST00000541363 | HMGA2 | chr12 | 66345163 | + | 7911 | 439 | 111 | 482 | 123 |
ENST00000308259 | MSRB3 | chr12 | 65762806 | + | ENST00000541363 | HMGA2 | chr12 | 66345163 | + | 8038 | 566 | 226 | 609 | 127 |
ENST00000540804 | MSRB3 | chr12 | 65762806 | + | ENST00000541363 | HMGA2 | chr12 | 66345163 | + | 7822 | 350 | 22 | 393 | 123 |
ENST00000535664 | MSRB3 | chr12 | 65762806 | + | ENST00000541363 | HMGA2 | chr12 | 66345163 | + | 8103 | 631 | 291 | 674 | 127 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000355192 | ENST00000541363 | MSRB3 | chr12 | 65762806 | + | HMGA2 | chr12 | 66345162 | + | 0.051865675 | 0.9481343 |
ENST00000308259 | ENST00000541363 | MSRB3 | chr12 | 65762806 | + | HMGA2 | chr12 | 66345162 | + | 0.022342343 | 0.9776577 |
ENST00000540804 | ENST00000541363 | MSRB3 | chr12 | 65762806 | + | HMGA2 | chr12 | 66345162 | + | 0.05077498 | 0.949225 |
ENST00000535664 | ENST00000541363 | MSRB3 | chr12 | 65762806 | + | HMGA2 | chr12 | 66345162 | + | 0.022148643 | 0.97785133 |
ENST00000355192 | ENST00000541363 | MSRB3 | chr12 | 65762806 | + | HMGA2 | chr12 | 66345163 | + | 0.051865675 | 0.9481343 |
ENST00000308259 | ENST00000541363 | MSRB3 | chr12 | 65762806 | + | HMGA2 | chr12 | 66345163 | + | 0.022342343 | 0.9776577 |
ENST00000540804 | ENST00000541363 | MSRB3 | chr12 | 65762806 | + | HMGA2 | chr12 | 66345163 | + | 0.05077498 | 0.949225 |
ENST00000535664 | ENST00000541363 | MSRB3 | chr12 | 65762806 | + | HMGA2 | chr12 | 66345163 | + | 0.022148643 | 0.97785133 |
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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 >55426_55426_1_MSRB3-HMGA2_MSRB3_chr12_65762806_ENST00000308259_HMGA2_chr12_66345162_ENST00000541363_length(amino acids)=127AA_BP=103 MPLFFASRFVGEDITVMSAFNLLHLVTKSQPVALRACGLPSGSCRDKKNCKVVFSQQELRKRLTPLQYHVTQEKGTESAFEGEYTHHKDP -------------------------------------------------------------- >55426_55426_2_MSRB3-HMGA2_MSRB3_chr12_65762806_ENST00000308259_HMGA2_chr12_66345163_ENST00000541363_length(amino acids)=127AA_BP=103 MPLFFASRFVGEDITVMSAFNLLHLVTKSQPVALRACGLPSGSCRDKKNCKVVFSQQELRKRLTPLQYHVTQEKGTESAFEGEYTHHKDP -------------------------------------------------------------- >55426_55426_3_MSRB3-HMGA2_MSRB3_chr12_65762806_ENST00000355192_HMGA2_chr12_66345162_ENST00000541363_length(amino acids)=123AA_BP=99 MPGLSMSPRRTLPRPLSLCLSLCLCLCLAAALGSAQSGSCRDKKNCKVVFSQQELRKRLTPLQYHVTQEKGTESAFEGEYTHHKDPGIYK -------------------------------------------------------------- >55426_55426_4_MSRB3-HMGA2_MSRB3_chr12_65762806_ENST00000355192_HMGA2_chr12_66345163_ENST00000541363_length(amino acids)=123AA_BP=99 MPGLSMSPRRTLPRPLSLCLSLCLCLCLAAALGSAQSGSCRDKKNCKVVFSQQELRKRLTPLQYHVTQEKGTESAFEGEYTHHKDPGIYK -------------------------------------------------------------- >55426_55426_5_MSRB3-HMGA2_MSRB3_chr12_65762806_ENST00000535664_HMGA2_chr12_66345162_ENST00000541363_length(amino acids)=127AA_BP=103 MPLFFASRFVGEDITVMSAFNLLHLVTKSQPVALRACGLPSGSCRDKKNCKVVFSQQELRKRLTPLQYHVTQEKGTESAFEGEYTHHKDP -------------------------------------------------------------- >55426_55426_6_MSRB3-HMGA2_MSRB3_chr12_65762806_ENST00000535664_HMGA2_chr12_66345163_ENST00000541363_length(amino acids)=127AA_BP=103 MPLFFASRFVGEDITVMSAFNLLHLVTKSQPVALRACGLPSGSCRDKKNCKVVFSQQELRKRLTPLQYHVTQEKGTESAFEGEYTHHKDP -------------------------------------------------------------- >55426_55426_7_MSRB3-HMGA2_MSRB3_chr12_65762806_ENST00000540804_HMGA2_chr12_66345162_ENST00000541363_length(amino acids)=123AA_BP=99 MPGLSMSPRRTLPRPLSLCLSLCLCLCLAAALGSAQSGSCRDKKNCKVVFSQQELRKRLTPLQYHVTQEKGTESAFEGEYTHHKDPGIYK -------------------------------------------------------------- >55426_55426_8_MSRB3-HMGA2_MSRB3_chr12_65762806_ENST00000540804_HMGA2_chr12_66345163_ENST00000541363_length(amino acids)=123AA_BP=99 MPGLSMSPRRTLPRPLSLCLSLCLCLCLAAALGSAQSGSCRDKKNCKVVFSQQELRKRLTPLQYHVTQEKGTESAFEGEYTHHKDPGIYK -------------------------------------------------------------- |
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Fusion Protein Functional Features |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr12:66232349/chr12:65856934) - 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 |
MSRB3 | HMGA2 |
FUNCTION: Catalyzes the reduction of free and protein-bound methionine sulfoxide to methionine. Isoform 2 is essential for hearing. {ECO:0000269|PubMed:14699060, ECO:0000269|PubMed:21185009}. | FUNCTION: Functions as a transcriptional regulator. Functions in cell cycle regulation through CCNA2. Plays an important role in chromosome condensation during the meiotic G2/M transition of spermatocytes. Plays a role in postnatal myogenesis, is involved in satellite cell activation (By similarity). Positively regulates IGF2 expression through PLAG1 and in a PLAG1-independent manner (PubMed:28796236). {ECO:0000250|UniProtKB:P52927, ECO:0000269|PubMed:14645522, ECO:0000269|PubMed:28796236}. |
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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 |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000354636 | 0 | 4 | 24_34 | 0 | 107.0 | DNA binding | Note=A.T hook 1 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000354636 | 0 | 4 | 44_54 | 0 | 107.0 | DNA binding | Note=A.T hook 2 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000354636 | 0 | 4 | 71_82 | 0 | 107.0 | DNA binding | Note=A.T hook 3 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000393578 | 0 | 4 | 24_34 | 0 | 91.0 | DNA binding | Note=A.T hook 1 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000393578 | 0 | 4 | 44_54 | 0 | 91.0 | DNA binding | Note=A.T hook 2 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000393578 | 0 | 4 | 71_82 | 0 | 91.0 | DNA binding | Note=A.T hook 3 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000425208 | 0 | 4 | 24_34 | 0 | 93.0 | DNA binding | Note=A.T hook 1 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000425208 | 0 | 4 | 44_54 | 0 | 93.0 | DNA binding | Note=A.T hook 2 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000425208 | 0 | 4 | 71_82 | 0 | 93.0 | DNA binding | Note=A.T hook 3 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000354636 | 0 | 4 | 24_34 | 0 | 107.0 | DNA binding | Note=A.T hook 1 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000354636 | 0 | 4 | 44_54 | 0 | 107.0 | DNA binding | Note=A.T hook 2 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000354636 | 0 | 4 | 71_82 | 0 | 107.0 | DNA binding | Note=A.T hook 3 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000393578 | 0 | 4 | 24_34 | 0 | 91.0 | DNA binding | Note=A.T hook 1 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000393578 | 0 | 4 | 44_54 | 0 | 91.0 | DNA binding | Note=A.T hook 2 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000393578 | 0 | 4 | 71_82 | 0 | 91.0 | DNA binding | Note=A.T hook 3 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000425208 | 0 | 4 | 24_34 | 0 | 93.0 | DNA binding | Note=A.T hook 1 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000425208 | 0 | 4 | 44_54 | 0 | 93.0 | DNA binding | Note=A.T hook 2 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000425208 | 0 | 4 | 71_82 | 0 | 93.0 | DNA binding | Note=A.T hook 3 |
- 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 | MSRB3 | chr12:65762806 | chr12:66345162 | ENST00000308259 | + | 5 | 7 | 47_169 | 97.33333333333333 | 186.0 | Domain | MsrB |
Hgene | MSRB3 | chr12:65762806 | chr12:66345162 | ENST00000355192 | + | 4 | 6 | 47_169 | 104.33333333333333 | 193.0 | Domain | MsrB |
Hgene | MSRB3 | chr12:65762806 | chr12:66345162 | ENST00000535664 | + | 6 | 8 | 47_169 | 97.33333333333333 | 186.0 | Domain | MsrB |
Hgene | MSRB3 | chr12:65762806 | chr12:66345163 | ENST00000308259 | + | 5 | 7 | 47_169 | 97.33333333333333 | 186.0 | Domain | MsrB |
Hgene | MSRB3 | chr12:65762806 | chr12:66345163 | ENST00000355192 | + | 4 | 6 | 47_169 | 104.33333333333333 | 193.0 | Domain | MsrB |
Hgene | MSRB3 | chr12:65762806 | chr12:66345163 | ENST00000535664 | + | 6 | 8 | 47_169 | 97.33333333333333 | 186.0 | Domain | MsrB |
Hgene | MSRB3 | chr12:65762806 | chr12:66345162 | ENST00000308259 | + | 5 | 7 | 189_192 | 97.33333333333333 | 186.0 | Motif | Endoplasmic reticulum retention signal |
Hgene | MSRB3 | chr12:65762806 | chr12:66345162 | ENST00000355192 | + | 4 | 6 | 189_192 | 104.33333333333333 | 193.0 | Motif | Endoplasmic reticulum retention signal |
Hgene | MSRB3 | chr12:65762806 | chr12:66345162 | ENST00000535664 | + | 6 | 8 | 189_192 | 97.33333333333333 | 186.0 | Motif | Endoplasmic reticulum retention signal |
Hgene | MSRB3 | chr12:65762806 | chr12:66345163 | ENST00000308259 | + | 5 | 7 | 189_192 | 97.33333333333333 | 186.0 | Motif | Endoplasmic reticulum retention signal |
Hgene | MSRB3 | chr12:65762806 | chr12:66345163 | ENST00000355192 | + | 4 | 6 | 189_192 | 104.33333333333333 | 193.0 | Motif | Endoplasmic reticulum retention signal |
Hgene | MSRB3 | chr12:65762806 | chr12:66345163 | ENST00000535664 | + | 6 | 8 | 189_192 | 97.33333333333333 | 186.0 | Motif | Endoplasmic reticulum retention signal |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000403681 | 2 | 5 | 24_34 | 83.0 | 110.0 | DNA binding | Note=A.T hook 1 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000403681 | 2 | 5 | 44_54 | 83.0 | 110.0 | DNA binding | Note=A.T hook 2 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000403681 | 2 | 5 | 71_82 | 83.0 | 110.0 | DNA binding | Note=A.T hook 3 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000403681 | 2 | 5 | 24_34 | 83.0 | 110.0 | DNA binding | Note=A.T hook 1 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000403681 | 2 | 5 | 44_54 | 83.0 | 110.0 | DNA binding | Note=A.T hook 2 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000403681 | 2 | 5 | 71_82 | 83.0 | 110.0 | DNA binding | Note=A.T hook 3 |
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Fusion Protein-Protein Interaction |
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Gene | PPI interactors |
HMGA2 | RELA, NFKB1, PIAS3, RB1, PRMT6, NPM1, SMAD1, SMAD5, SMAD9, PRKCA, HDGF, PTBP1, APEX1, SYNCRIP, XRCC6, PSIP1, PA2G4, PCBP2, E4F1, OBSL1, HIST1H3A, CREB1, NFATC1, PCGF1, POU5F1, DLST, EZH2, SUZ12, MYC, TP53, MDM2, CSK, VRK1, HIST1H1B, PRKAG2, DUX4, DUX4L9, SYDE1, ARHGAP21, ARHGAP39, Plekhg5, ZNF263, MAFB, KAT2B, HIST1H2BG, LMNB1, NDUFAF7, CSNK2A1, LIG3, SUPT16H, VRK3, SP2, C1QBP, PARP2, TOP3A, CSNK2A2, XPC, RANBP17, PARP1, SUPV3L1, HIST2H2AC, HIST2H3PS2, KPNA4, USP7, |
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Gene | STRING network |
MSRB3 | |
HMGA2 | ![]() |
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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 |
Tgene | HMGA2 | chr12:65762806 | chr12:66345162 | ENST00000403681 | 2 | 5 | 44_63 | 83.0 | 110.0 | E4F1 | |
Tgene | HMGA2 | chr12:65762806 | chr12:66345163 | ENST00000403681 | 2 | 5 | 44_63 | 83.0 | 110.0 | E4F1 |
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Related Drugs to MSRB3-HMGA2 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to MSRB3-HMGA2 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | HMGA2 | C1519176 | Salivary Gland Pleomorphic Adenoma | 2 | ORPHANET |
Tgene | HMGA2 | C0005612 | Birth Weight | 1 | CTD_human |
Tgene | HMGA2 | C0006826 | Malignant Neoplasms | 1 | CTD_human |
Tgene | HMGA2 | C0027626 | Neoplasm Invasiveness | 1 | CTD_human |
Tgene | HMGA2 | C0027651 | Neoplasms | 1 | CTD_human |
Tgene | HMGA2 | C0086692 | Benign Neoplasm | 1 | CTD_human |
Tgene | HMGA2 | C0175693 | Russell-Silver syndrome | 1 | GENOMICS_ENGLAND |
Tgene | HMGA2 | C0473935 | Radiolabeled somatostatin analog study | 1 | GENOMICS_ENGLAND |
Tgene | HMGA2 | C0796160 | MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE | 1 | GENOMICS_ENGLAND |
Tgene | HMGA2 | C1096309 | Myolipoma | 1 | GENOMICS_ENGLAND |
Tgene | HMGA2 | C4305140 | 12q14 microdeletion syndrome | 1 | ORPHANET |