Fusion partner gene information | Fusion gene name: MECOM-LPP |
FusionPDB ID: 52502 | FusionGDB2.0 ID: 52502 | | Hgene | Tgene | Gene symbol | MECOM | LPP | Gene ID | 2122 | 4026 | Gene name | MDS1 and EVI1 complex locus | LIM domain containing preferred translocation partner in lipoma |
Synonyms | AML1-EVI-1|EVI1|KMT8E|MDS1|MDS1-EVI1|PRDM3|RUSAT2 | - |
Cytomap | 3q26.2 | 3q27.3-q28 |
Type of gene | protein-coding | protein-coding |
Description | histone-lysine N-methyltransferase MECOMAML1-EVI-1 fusion proteinMDS1 and EVI1 complex locus protein EVI1MDS1 and EVI1 complex locus protein MDS1PR domain 3ecotropic virus integration site 1 protein homologmyelodysplasia syndrome-associated protein | lipoma-preferred partnerLIM proteinlipoma preferred partner |
Modification date | 20200313 | 20200313 |
UniProtAcc | Q03112 Main function of 5'-partner protein: FUNCTION: [Isoform 1]: Functions as a transcriptional regulator binding to DNA sequences in the promoter region of target genes and regulating positively or negatively their expression. Oncogene which plays a role in development, cell proliferation and differentiation. May also play a role in apoptosis through regulation of the JNK and TGF-beta signaling. Involved in hematopoiesis. {ECO:0000269|PubMed:10856240, ECO:0000269|PubMed:11568182, ECO:0000269|PubMed:15897867, ECO:0000269|PubMed:16462766, ECO:0000269|PubMed:19767769, ECO:0000269|PubMed:9665135}.; FUNCTION: [Isoform 7]: Displays histone methyltransferase activity and monomethylates 'Lys-9' of histone H3 (H3K9me1) in vitro. Probably catalyzes the monomethylation of free histone H3 in the cytoplasm which is then transported to the nucleus and incorporated into nucleosomes where SUV39H methyltransferases use it as a substrate to catalyze histone H3 'Lys-9' trimethylation. Likely to be one of the primary histone methyltransferases along with PRDM16 that direct cytoplasmic H3K9me1 methylation. {ECO:0000250|UniProtKB:P14404}. | Q93052 Main function of 5'-partner protein: FUNCTION: May play a structural role at sites of cell adhesion in maintaining cell shape and motility. In addition to these structural functions, it may also be implicated in signaling events and activation of gene transcription. May be involved in signal transduction from cell adhesion sites to the nucleus allowing successful integration of signals arising from soluble factors and cell-cell adhesion sites. Also suggested to serve as a scaffold protein upon which distinct protein complexes are assembled in the cytoplasm and in the nucleus. {ECO:0000269|PubMed:10637295}. |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000494292, ENST00000485957, ENST00000264674, ENST00000392736, ENST00000433243, ENST00000460814, ENST00000464456, ENST00000468789, ENST00000472280, | ENST00000471917, ENST00000312675, ENST00000448637, ENST00000543006, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 33 X 21 X 11=7623 | 25 X 27 X 9=6075 |
# samples | 43 | 34 |
** MAII score | log2(43/7623*10)=-4.14795031118505 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(34/6075*10)=-4.1592777572428 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 |
Fusion gene context | PubMed: MECOM [Title/Abstract] AND LPP [Title/Abstract] AND fusion [Title/Abstract] |
Fusion neoantigen context | PubMed: MECOM [Title/Abstract] AND LPP [Title/Abstract] AND neoantigen [Title/Abstract] |
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | MECOM(169381124)-LPP(188242453), # samples:1
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Anticipated loss of major functional domain due to fusion event. | MECOM-LPP 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. MECOM-LPP 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. MECOM-LPP 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. MECOM-LPP 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.
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Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | MECOM | C4225221 | RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2 | 3 | GENOMICS_ENGLAND;UNIPROT |
Hgene | MECOM | C0006142 | Malignant neoplasm of breast | 1 | CTD_human |
Hgene | MECOM | C0007102 | Malignant tumor of colon | 1 | CTD_human |
Hgene | MECOM | C0009375 | Colonic Neoplasms | 1 | CTD_human |
Hgene | MECOM | C0023448 | Lymphoid leukemia | 1 | CTD_human |
Hgene | MECOM | C0023466 | Leukemia, Monocytic, Chronic | 1 | CTD_human |
Hgene | MECOM | C0023467 | Leukemia, Myelocytic, Acute | 1 | CTD_human |
Hgene | MECOM | C0023470 | Myeloid Leukemia | 1 | CTD_human |
Hgene | MECOM | C0026998 | Acute Myeloid Leukemia, M1 | 1 | CTD_human |
Hgene | MECOM | C0027022 | Myeloproliferative disease | 1 | CTD_human |
Hgene | MECOM | C0027439 | Nasopharyngeal Neoplasms | 1 | CTD_human |
Hgene | MECOM | C0030312 | Pancytopenia | 1 | CTD_human |
Hgene | MECOM | C0038002 | Splenomegaly | 1 | CTD_human |
Hgene | MECOM | C0238301 | Cancer of Nasopharynx | 1 | CTD_human |
Hgene | MECOM | C0678222 | Breast Carcinoma | 1 | CTD_human |
Hgene | MECOM | C0919267 | ovarian neoplasm | 1 | CTD_human |
Hgene | MECOM | C1140680 | Malignant neoplasm of ovary | 1 | CTD_human |
Hgene | MECOM | C1257931 | Mammary Neoplasms, Human | 1 | CTD_human |
Hgene | MECOM | C1458155 | Mammary Neoplasms | 1 | CTD_human |
Hgene | MECOM | C1854273 | Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia | 1 | GENOMICS_ENGLAND;ORPHANET |
Hgene | MECOM | C1879321 | Acute Myeloid Leukemia (AML-M2) | 1 | CTD_human |
Hgene | MECOM | C2931456 | Prostate cancer, familial | 1 | CTD_human |
Hgene | MECOM | C4704874 | Mammary Carcinoma, Human | 1 | CTD_human |
Hgene | MECOM | C4722327 | PROSTATE CANCER, HEREDITARY, 1 | 1 | CTD_human |
Tgene | LPP | C0087031 | Juvenile-Onset Still Disease | 1 | CTD_human |
Tgene | LPP | C3495559 | Juvenile arthritis | 1 | CTD_human |
Tgene | LPP | C3714758 | Juvenile psoriatic arthritis | 1 | CTD_human |
Tgene | LPP | C4552091 | Polyarthritis, Juvenile, Rheumatoid Factor Negative | 1 | CTD_human |
Tgene | LPP | C4704862 | Polyarthritis, Juvenile, Rheumatoid Factor Positive | 1 | CTD_human |