hemiparesis Gene Set
Genes
14 genes associated with the hemiparesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ATP1A2
|
ATPase, Na+/K+ transporting, alpha 2 polypeptide
|
|
CACNA1A
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
|
|
COL4A1
|
collagen, type IV, alpha 1
|
|
GUCY1A3
|
guanylate cyclase 1, soluble, alpha 3
|
|
PRNP
|
prion protein
|
|
SCN1A
|
sodium channel, voltage gated, type I alpha subunit
|
|
SLC1A3
|
solute carrier family 1 (glial high affinity glutamate transporter), member 3
|
|
SLC2A1
|
solute carrier family 2 (facilitated glucose transporter), member 1
|
|
TBC1D24
|
TBC1 domain family, member 24
|
|
TREX1
|
three prime repair exonuclease 1
|
|
TSC1
|
tuberous sclerosis 1
|
|
TTR
|
transthyretin
|
|
TUBB2B
|
tubulin, beta 2B class IIb
|
|
WDR62
|
WD repeat domain 62
|
