bradykinesia Gene Set
Genes
27 gene mutations causing the bradykinesia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ADCY5
|
adenylate cyclase 5
|
|
ATP2A2
|
ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
|
|
BAHCC1
|
BAH domain and coiled-coil containing 1
|
|
BCAT2
|
branched chain amino-acid transaminase 2, mitochondrial
|
|
CTSD
|
cathepsin D
|
|
CYP19A1
|
cytochrome P450, family 19, subfamily A, polypeptide 1
|
|
DRD2
|
dopamine receptor D2
|
|
FOXP2
|
forkhead box P2
|
|
FOXP3
|
forkhead box P3
|
|
GLI2
|
GLI family zinc finger 2
|
|
HEXB
|
hexosaminidase B (beta polypeptide)
|
|
HTRA2
|
HtrA serine peptidase 2
|
|
HTT
|
huntingtin
|
|
IREB2
|
iron-responsive element binding protein 2
|
|
LMNA
|
lamin A/C
|
|
LTN1
|
listerin E3 ubiquitin protein ligase 1
|
|
NTAN1
|
N-terminal asparagine amidase
|
|
PARK7
|
parkinson protein 7
|
|
PEX13
|
peroxisomal biogenesis factor 13
|
|
SIX1
|
SIX homeobox 1
|
|
SLC18A2
|
solute carrier family 18 (vesicular monoamine transporter), member 2
|
|
SLC6A9
|
solute carrier family 6 (neurotransmitter transporter, glycine), member 9
|
|
SPR
|
sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase)
|
|
SYNGAP1
|
synaptic Ras GTPase activating protein 1
|
|
TH
|
tyrosine hydroxylase
|
|
UBE3A
|
ubiquitin protein ligase E3A
|
|
UNC79
|
unc-79 homolog (C. elegans)
|
