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FLASH GENE
Symbol MID2 contributors: KTN/npt - updated : 02-02-2009
HGNC name midline 2
HGNC id 7096
EXPRESSION
Type
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Endocrinepancreas    
Nervousbrain    
Urinarykidney    
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Epithelialsecretoryglandularendocrine 
Epithelialsecretoryglandularexocrine 
cell lineage
cell lines
fluid/secretion
at STAGE
physiological period fetal, pregnancy
Text tissues, noteworthy in developing heart
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • an N terminal RING finger
  • two B box domains, linked to a leucine coiled-coil domain (RBCC subgroup) the so-called tripartite motif (TRIM) mediating homodimerization, characteristic of the B box family of proteins, involved in cell proliferation and development
  • a COS (C-terminal subgrooup one signature) domain
  • a fibronectin type III domain between the RBCC
  • the C terminal B30-2/SPRY or RFP-like domain
  • conjugated PhosphoP
    mono polymer homomer , heteromer , dimer
    HOMOLOGY
    interspecies homolog to murine Mid2 (99.3 pc)
    homolog to rattus Mid2 (99.1 pc)
    intraspecies homolog to MID1
    Homologene
    FAMILY
  • TRIM/RBCC family
  • B box family TRIM subfamily
  • CATEGORY structural protein
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm,cytoskeleton,microtubule
    basic FUNCTION
  • playing a role in embryonic development
  • acting as an antiretroviral factor (Ozato 2008)
  • CELLULAR PROCESS cell life, proliferation/growth
    PHYSIOLOGICAL PROCESS development
    PATHWAY
    metabolism
    signaling
    a component
  • heterodimer with MID1 (Short 2002)
  • INTERACTION
    DNA
    RNA
    small molecule metal binding,
  • Zn2+
  • protein
  • interacting with IGBP1
  • interacting with PPP2R4 (Short 2002)
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Susceptibility
    Variant & Polymorphism
    Candidate gene for X-linked FG (Opitz-Kaveggia) syndrome (Short 2002, Ozato 2008)
    Marker
    Therapy target
    ANIMAL & CELL MODELS