Spondylolysis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A bone structure disease that involves a defect located_in lumbar vertebral column. (Human Disease Ontology, DOID_2300)
External Link https://www.disgenet.org/browser/0/1/0/C0038018
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Genes

9 genes associated with the disease Spondylolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AGA aspartylglucosaminidase
BMP7 bone morphogenetic protein 7
CTSK cathepsin K
FLNA filamin A, alpha
FLNB filamin B, beta
GDF5 growth differentiation factor 5
PIEZO2 piezo-type mechanosensitive ion channel component 2
RUNX2 runt-related transcription factor 2
SLC26A2 solute carrier family 26 (anion exchanger), member 2