osteoporosis Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A bone resorption disease that has_material_basis_in a drop in estrogen or testosterone which results_in the thinning of bone tissue and loss of bone mineral density. (Human Disease Ontology, DOID_11476)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0000939
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Genes

19 genes associated with the osteoporosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
NRCAM neuronal cell adhesion molecule 1.1784
ALDH7A1 aldehyde dehydrogenase 7 family, member A1 0.676552
FTCDNL1 formiminotransferase cyclodeaminase N-terminal like 0.542759
COL4A2 collagen, type IV, alpha 2 0.535899
MECOM MDS1 and EVI1 complex locus 0.522136
RAP1A RAP1A, member of RAS oncogene family 0.522136
TBC1D8 TBC1 domain family, member 8 (with GRAM domain) 0.495598
AKAP6 A kinase (PRKA) anchor protein 6 0.485436
OSBPL1A oxysterol binding protein-like 1A 0.450694
SOX6 SRY (sex determining region Y)-box 6 0.450694
DOK6 docking protein 6 0.426113
TNR tenascin R 0.424465
MCM8 minichromosome maintenance complex component 8 0.417822
PIGZ phosphatidylinositol glycan anchor biosynthesis, class Z 0.408813
WDFY4 WDFY family member 4 0.407869
TBC1D22A TBC1 domain family, member 22A 0.403739
EEF1DP3 eukaryotic translation elongation factor 1 delta pseudogene 3 0.384893
LIN28B lin-28 homolog B (C. elegans) 0.378074
LRP1B low density lipoprotein receptor-related protein 1B 0.352621