hemiplegia Gene Set
Genes
12 genes associated with the hemiplegia 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
|
|
ATP1A3
|
ATPase, Na+/K+ transporting, alpha 3 polypeptide
|
|
CACNA1A
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
|
|
CECR1
|
cat eye syndrome chromosome region, candidate 1
|
|
COL4A1
|
collagen, type IV, alpha 1
|
|
COL4A2
|
collagen, type IV, alpha 2
|
|
CTC1
|
CTS telomere maintenance complex component 1
|
|
DOCK8
|
dedicator of cytokinesis 8
|
|
PRF1
|
perforin 1 (pore forming protein)
|
|
SCN1A
|
sodium channel, voltage gated, type I alpha subunit
|
|
SLC1A3
|
solute carrier family 1 (glial high affinity glutamate transporter), member 3
|
|
SUOX
|
sulfite oxidase
|
