abnormal intraocular pressure Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly in the amount of force per unit area exerted by the intraocular fluid within the eye. (Human Phenotype Ontology, HP_0012632)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0012632
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Genes

16 genes associated with the abnormal intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
GAS7 growth arrest-specific 7 1.24751
TMCO1 transmembrane and coiled-coil domains 1 1.21853
FAT3 FAT atypical cadherin 3 1.1213
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive) 1.0674
SLC30A8 solute carrier family 30 (zinc transporter), member 8 1.00059
PDE7B phosphodiesterase 7B 1.00059
LRRC4C leucine rich repeat containing 4C 0.980125
CSF1R colony stimulating factor 1 receptor 0.977911
BMPR1A bone morphogenetic protein receptor, type IA 0.969142
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1 0.942765
FOXP1 forkhead box P1 0.919744
LOC100147773 uncharacterized LOC100147773 0.876787
SATB1 SATB homeobox 1 0.853087
AFAP1 actin filament associated protein 1 0.844241
CRMP1 collapsin response mediator protein 1 0.724077
ATP8B5P ATPase, class I, type 8B, member 5, pseudogene 0.472791