Human Gene MECOM (ENST00000494292.6) Description and Page Index
  Description: Homo sapiens MDS1 and EVI1 complex locus (MECOM), transcript variant 15, mRNA. (from RefSeq NM_001366473)
Gencode Transcript: ENST00000494292.6
Gencode Gene: ENSG00000085276.19
Transcript (Including UTRs)
   Position: hg38 chr3:169,084,761-169,663,775 Size: 579,015 Total Exon Count: 16 Strand: -
Coding Region
   Position: hg38 chr3:169,084,909-169,663,372 Size: 578,464 Coding Exon Count: 16 

Page IndexSequence and LinksUniProtKB CommentsProtein StructureOther NamesMethods
Data last updated at UCSC: 2021-06-20 19:51:40

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr3:169,084,761-169,663,775)mRNA (may differ from genome)Protein (1230 aa)
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HGNCMGIPubMedUniProtKB

-  Comments and Description Text from UniProtKB
  ID: EVI1_HUMAN
DESCRIPTION: RecName: Full=MDS1 and EVI1 complex locus protein EVI1; AltName: Full=Ecotropic virus integration site 1 protein homolog; Short=EVI-1;
FUNCTION: 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.
SUBUNIT: Homooligomer. Interacts with SUV39H1 (via SET domain); enhances MECOM transcriptional repression activity (By similarity). Interacts with CTBP1. Interacts with SMAD3 (via MH2 domain); the interaction is direct. Interacts with SMAD4; through interaction with SMAD3. Interacts with CREBBP, KAT2B and histone deacetylases. Interacts with MAPK8 and MAPK9; inhibits JNK signaling.
INTERACTION: P56546:Ctbp2 (xeno); NbExp=3; IntAct=EBI-1384862, EBI-1384883; Q96EB6:SIRT1; NbExp=2; IntAct=EBI-1384862, EBI-1802965; Q9UBK9:UXT; NbExp=5; IntAct=EBI-1384862, EBI-357355;
SUBCELLULAR LOCATION: Nucleus. Nucleus speckle.
DOMAIN: Both zinc finger regions are required for the transcriptional activation of PBX1.
PTM: Phosphorylated (By similarity). Phosphorylated upon DNA damage, probably by ATM or ATR.
PTM: May be acetylated by CREBBP and KAT2B.
DISEASE: Note=A chromosomal aberration involving EVI1 is a cause of chronic myelogenous leukemia (CML). Translocation t(3;21)(q26;q22) with RUNX1/AML1.
SIMILARITY: Contains 10 C2H2-type zinc fingers.
SEQUENCE CAUTION: Sequence=AAB29907.1; Type=Erroneous initiation; Sequence=AAB37456.1; Type=Miscellaneous discrepancy; Note=Probable cloning artifact; Sequence=AAI30521.1; Type=Erroneous initiation; Sequence=BAH14103.1; Type=Miscellaneous discrepancy; Note=Aberrant splicing;
WEB RESOURCE: Name=Atlas of Genetics and Cytogenetics in Oncology and Haematology; URL="http://atlasgeneticsoncology.org/Genes/EVI103q26ID19.html";

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR007087 - Znf_C2H2
IPR015880 - Znf_C2H2-like
IPR013087 - Znf_C2H2/integrase_DNA-bd

Pfam Domains:
PF00096 - Zinc finger, C2H2 type

ModBase Predicted Comparative 3D Structure on Q03112
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-  Other Names for This Gene
  UCSC ID: ENST00000494292.6
Representative RNA: NM_001366473
Protein: Q03112 (aka EVI1_HUMAN)

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.