osteolytic defects of the phalanges of the hand Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Dissolution or degeneration of bone tissue of the phalanges of the hand. (Human Phenotype Ontology, HP_0009771)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009771
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Genes

12 genes associated with the osteolytic defects of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATL3 atlastin GTPase 3
BANF1 barrier to autointegration factor 1
COL3A1 collagen, type III, alpha 1
CTSC cathepsin C
CTSK cathepsin K
FAM134B family with sequence similarity 134, member B
FLNA filamin A, alpha
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
LMNA lamin A/C
NOTCH2 notch 2
WNK1 WNK lysine deficient protein kinase 1
ZMPSTE24 zinc metallopeptidase STE24
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