impaired proprioception Gene Set
Genes
14 genes associated with the impaired proprioception phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
C10ORF2
|
chromosome 10 open reading frame 2
|
|
CYP7B1
|
cytochrome P450, family 7, subfamily B, polypeptide 1
|
|
EGR2
|
early growth response 2
|
|
FLVCR1
|
feline leukemia virus subgroup C cellular receptor 1
|
|
FXN
|
frataxin
|
|
GPI
|
glucose-6-phosphate isomerase
|
|
MFN2
|
mitofusin 2
|
|
MPZ
|
myelin protein zero
|
|
PMP22
|
peripheral myelin protein 22
|
|
POLG
|
polymerase (DNA directed), gamma
|
|
PRX
|
periaxin
|
|
RNF170
|
ring finger protein 170
|
|
SETX
|
senataxin
|
|
TBP
|
TATA box binding protein
|
