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FLASH GENE
Symbol NOL3 contributors: mct - updated : 29/10/2008
HGNC name nucleolar protein 3 (apoptosis repressor with CARD domain)
HGNC id 7869
EXPRESSION
Type restricted
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Cardiovascularheart   predominantly Homo sapiens
Digestivesalivary gland   highly
Endocrineneuroendocrinepituitary  highly
 parathyroid   highly
Nervousnerve   highly
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Connectiveadipose  highly
Muscularstriatumskeletal predominantly Homo sapiens
Muscularstriatumcardiac predominantly Homo sapiens
cells
SystemCellPubmedSpeciesStageRna symbol
Muscularmyocyte Homo sapiens
Nervousneuron Homo sapiens
cell lineage
cell lines
fluid/secretion
at STAGE
physiological period pregnancy
Text placenta
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • an N terminal caspase recruitment domain (CARD)
  • a C terminal region rich in proline and glutamic acid
  • mono polymer polymer
    HOMOLOGY
    interspecies homolog to rattus Nol3 (85.4 pc)
    homolog to murine Nol3 (85.1 pc)
    Homologene
    FAMILY
    CATEGORY regulatory
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm,cytosolic
    intracellular,nucleus,nucleoplasm
    intracellular,nucleus,nucleolus
    basic FUNCTION
  • involved in alternative splice site selection
  • inhibiting caspase 2 and 8
  • being a Ca(2+)-dependent regulator of caspase 8 and cell death
  • inhibitor of apoptosis in that it antagonizes both the extrinsic (death receptor) and intrinsic (mitochondrial/ER) apoptosis pathways
  • CELLULAR PROCESS cell life, antiapoptosis
    nucleotide, RNA splicing
    PHYSIOLOGICAL PROCESS
    text regulation of apoptosis
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA binding
    small molecule metal binding,
  • Ca2+
  • protein
  • alternating apoptosis induced by TRADD, FADD
  • binding to the RS domain of SFRS9 (Srp30c)
  • interacting with TFPT
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Other morbid association(s)
    TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
    tumoral     --over  
    in the epithelium of primary breast cancers compared with benign breast tissue and to confer chemo- and radiation-resistance
    tumoral     --over  
    in most colon cancer cell lines and in almost all primary colon cancers compared with corresponding controls
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker marker of human colon cancer
    Therapy target
    ANIMAL & CELL MODELS