spastic gait Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002064
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Genes

29 genes associated with the spastic gait phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
AP5Z1 adaptor-related protein complex 5, zeta 1 subunit
ATL1 atlastin GTPase 1
B4GALNT1 beta-1,4-N-acetyl-galactosaminyl transferase 1
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CCT5 chaperonin containing TCP1, subunit 5 (epsilon)
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
GBA2 glucosidase, beta (bile acid) 2
GJC2 gap junction protein, gamma 2, 47kDa
HSPD1 heat shock 60kDa protein 1 (chaperonin)
KCNA1 potassium channel, voltage gated shaker related subfamily A, member 1
KIAA0196 KIAA0196
KIF1A kinesin family member 1A
KIF5A kinesin family member 5A
MECP2 methyl CpG binding protein 2
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
NT5C2 5'-nucleotidase, cytosolic II
PLP1 proteolipid protein 1
REEP1 receptor accessory protein 1
REEP2 receptor accessory protein 2
RTN2 reticulon 2
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1
SPAST spastin
SPG11 spastic paraplegia 11 (autosomal recessive)
SPG20 spastic paraplegia 20 (Troyer syndrome)
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
TECPR2 tectonin beta-propeller repeat containing 2
ZFYVE26 zinc finger, FYVE domain containing 26
ZFYVE27 zinc finger, FYVE domain containing 27