amblyopia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000646
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Genes

14 genes associated with the amblyopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GAT3 beta-1,3-glucuronyltransferase 3
CHN1 chimerin 1
COL4A1 collagen, type IV, alpha 1
CRYAA crystallin, alpha A
CRYGC crystallin, gamma C
GPR143 G protein-coupled receptor 143
LAMA1 laminin, alpha 1
NPHP4 nephronophthisis 4
PHOX2A paired-like homeobox 2a
PTEN phosphatase and tensin homolog
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SOBP sine oculis binding protein homolog (Drosophila)
TBX1 T-box 1
TUBB3 tubulin, beta 3 class III