impaired vibration sensation in the lower limbs Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A decrease in the ability to perceive vibration in the legs. (Human Phenotype Ontology, HP_0002166)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002166
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Genes

16 genes associated with the impaired vibration sensation in the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATL1 atlastin GTPase 1
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
FLVCR1 feline leukemia virus subgroup C cellular receptor 1
GBA2 glucosidase, beta (bile acid) 2
HSPD1 heat shock 60kDa protein 1 (chaperonin)
KIAA0196 KIAA0196
KIF5A kinesin family member 5A
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
PDYN prodynorphin
PRKCG protein kinase C, gamma
RTN2 reticulon 2
SACS sacsin molecular chaperone
SPAST spastin
SPG11 spastic paraplegia 11 (autosomal recessive)
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)