primary congenital glaucoma Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Xref MGI. (Human Disease Ontology, DOID_0050593)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0008007
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Genes

16 genes associated with the primary congenital glaucoma 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