akinesia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Inability to initiate changes in activity or movement and to perform ordinary volitional movements rapidly and easily. (Human Phenotype Ontology, HP_0002304)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002690
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Genes

17 gene mutations causing the akinesia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRG6 adhesion G protein-coupled receptor G6
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase)
DOK7 docking protein 7
DRD2 dopamine receptor D2
GBA glucosidase, beta, acid
HTRA2 HtrA serine peptidase 2
INPP4A inositol polyphosphate-4-phosphatase, type I, 107kDa
INS insulin
LGI1 leucine-rich, glioma inactivated 1
MAP6 microtubule-associated protein 6
MECP2 methyl CpG binding protein 2
NR4A2 nuclear receptor subfamily 4, group A, member 2
SCN1A sodium channel, voltage gated, type I alpha subunit
SLC12A5 solute carrier family 12 (potassium/chloride transporter), member 5
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SNAP25 synaptosomal-associated protein, 25kDa
VAMP1 vesicle-associated membrane protein 1 (synaptobrevin 1)