spondylolysis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A bone structure disease that involves a defect located_in lumbar vertebral column. (Human Disease Ontology, DOID_2300)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003304
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Genes

5 genes associated with the spondylolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGA aspartylglucosaminidase
CTSK cathepsin K
FLNA filamin A, alpha
FLNB filamin B, beta
RUNX2 runt-related transcription factor 2