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)