diminished movement Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002374
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Genes

19 genes associated with the diminished movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
ATP13A2 ATPase type 13A2
CHRNA1 cholinergic receptor, nicotinic, alpha 1 (muscle)
CHRND cholinergic receptor, nicotinic, delta (muscle)
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
CNTN1 contactin 1
ERBB3 erb-b2 receptor tyrosine kinase 3
GBA glucosidase, beta, acid
GFM1 G elongation factor, mitochondrial 1
GLRA1 glycine receptor, alpha 1
LAMP2 lysosomal-associated membrane protein 2
MAPT microtubule-associated protein tau
MRPS16 mitochondrial ribosomal protein S16
MTM1 myotubularin 1
PANK2 pantothenate kinase 2
PDE8B phosphodiesterase 8B
SLC52A2 solute carrier family 52 (riboflavin transporter), member 2
TH tyrosine hydroxylase
VPS35 vacuolar protein sorting 35 homolog (S. cerevisiae)