bone cyst Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A fluid filled cavity that develops with a bone. (Human Phenotype Ontology, HP_0012062)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012062
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Genes

18 genes associated with the bone cyst phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AKT1 v-akt murine thymoma viral oncogene homolog 1
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CAV1 caveolin 1, caveolae protein, 22kDa
FOS FBJ murine osteosarcoma viral oncogene homolog
KLLN killin, p53-regulated DNA replication inhibitor
NOTCH3 notch 3
PDGFRB platelet-derived growth factor receptor, beta polypeptide
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PTCH1 patched 1
PTEN phosphatase and tensin homolog
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
TREM2 triggering receptor expressed on myeloid cells 2
TYROBP TYRO protein tyrosine kinase binding protein
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
ZBTB20 zinc finger and BTB domain containing 20