diminished movement Gene Set
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)
|
