Amblyopia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D000550
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Genes

6 genes/proteins associated with the disease Amblyopia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2 1.17464
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha 1.10388
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1 1.09822
PTGDS prostaglandin D2 synthase 21kDa (brain) 1.09716
MAPK3 mitogen-activated protein kinase 3 1.04611
RALGAPA1 Ral GTPase activating protein, alpha subunit 1 (catalytic) 1.02225