abnormality of binocular vision Gene Set
Genes
10 genes associated with the abnormality of binocular vision 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
|
ATXN3
|
ataxin 3
|
CACNA1A
|
calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
|
MAPT
|
microtubule-associated protein tau
|
PRNP
|
prion protein
|
PTPN22
|
protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
|
SERPINI1
|
serpin peptidase inhibitor, clade I (neuroserpin), member 1
|
SLC2A1
|
solute carrier family 2 (facilitated glucose transporter), member 1
|
TGFB1
|
transforming growth factor, beta 1
|
TPP1
|
tripeptidyl peptidase I
|