abnormal pupillary function Gene Set
Genes
9 genes associated with the abnormal pupillary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACTA2
|
actin, alpha 2, smooth muscle, aorta
|
|
DDC
|
dopa decarboxylase (aromatic L-amino acid decarboxylase)
|
|
MPZ
|
myelin protein zero
|
|
NME1
|
NME/NM23 nucleoside diphosphate kinase 1
|
|
ORAI1
|
ORAI calcium release-activated calcium modulator 1
|
|
PHYH
|
phytanoyl-CoA 2-hydroxylase
|
|
SH3TC2
|
SH3 domain and tetratricopeptide repeats 2
|
|
SIX6
|
SIX homeobox 6
|
|
STIM1
|
stromal interaction molecule 1
|
