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Symbol SPG21 contributors: mct/shn - updated : 03-08-2010
HGNC name spastic paraplegia 21 (autosomal recessive, Mast syndrome)
HGNC id 20373
Corresponding disease
SPG21 spastic paraplegia 21
Location 15q22.31      Physical location : 65.255.363 - 65.282.251
Synonym name
  • maspardin
  • acid cluster protein 33
  • Synonym symbol(s) GLO10, MAST, ACP33, BM-019
    DNA
    TYPE functioning gene
    STRUCTURE 26.89 kb     9 Exon(s)
    MAPPING cloned Y linked N status provisional
    Map cen - D15S1009 - D15S108 - SPG21 SPG21 - D15S1507 - D15S1020 - qter
    RNA
    TRANSCRIPTS type messenger
    identificationnb exonstypebpproduct
    ProteinkDaAAspecific expressionYearPubmed
    8 splicing 1734 - 281 - Simpson et al, 2003
    9 splicing 1815 33 308 - Simpson et al, 2003
    9 splicing 1635 - 308 - Simpson (2003)
    EXPRESSION
    Type
       expressed in (based on citations)
    organ(s)
    SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
    Endocrinepancreas    
    Nervousbrain    
    Reproductivemale systemprostate   
    Respiratorylung    
    Skin/Tegumentskin    
    Urinarykidney    
    tissue
    SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
    Connectivebone   
    Muscularstriatumskeletal  
    cell lineage
    cell lines
    fluid/secretion
    at STAGE
    PROTEIN
    PHYSICAL PROPERTIES
    STRUCTURE
    motifs/domains
    HOMOLOGY
    interspecies ortholog to Spg21, Mus musculus
    ortholog to SPG21, Pan troglodytes
    ortholog to Spg21, Rattus norvegicus
    ortholog to spg21, Danio rerio
    Homologene
    FAMILY
  • AB hydrolase superfamily
  • CATEGORY regulatory , receptor membrane
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm,organelle,Golgi
    intracellular,cytoplasm,organelle,endosome
    text
  • localizes prominently to cytoplasm as well as to membranes, possibly at trans-Golgi network/late endosomal compartments (Hanna 2008)
  • localize to the endosomal membrane traffic compartment, suggesting that the long axons of the corticospinal tract may be especially vulnerable to endosomal dysfunction (Tsang 2009)
  • basic FUNCTION
  • ligand of CD4 (Zeitlmann 2001)
  • aldehyde dehydrogenase ALDH16A1 (Hanna 2009)
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein
  • binding to CD4
  • interacting with the aldehyde dehydrogenase ALDH16A1 (Hanna 2008)
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) SPG21
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS
  • SPG21-/- knockout mice are normal at birth, within several months they develop gradually progressive hind limb dysfunction and display alterations in axon branching in cultured cerebral cortical neurons (Soderblom et al, 2010)