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FLASH GENE
Symbol SPG21 contributors: mct/shn - updated : 03-08-2010
HGNC name spastic paraplegia 21 (autosomal recessive, Mast syndrome)
HGNC id 20373
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)