Spastic Paraplegia, Hereditary Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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21 genes associated with the Spastic Paraplegia, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AP5Z1 adaptor-related protein complex 5, zeta 1 subunit
ATL1 atlastin GTPase 1
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
C9ORF72 chromosome 9 open reading frame 72
DDHD2 DDHD domain containing 2
DPP6 dipeptidyl-peptidase 6
FA2H fatty acid 2-hydroxylase
HSPD1 heat shock 60kDa protein 1 (chaperonin)
KIF5A kinesin family member 5A
L1CAM L1 cell adhesion molecule
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
PLP1 proteolipid protein 1
REEP1 receptor accessory protein 1
SPAST spastin
SPG11 spastic paraplegia 11 (autosomal recessive)
SPG20 spastic paraplegia 20 (Troyer syndrome)
SPG21 spastic paraplegia 21 (autosomal recessive, Mast syndrome)
SPG41 spastic paraplegia 41 (autosomal dominant)
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
ZFYVE26 zinc finger, FYVE domain containing 26