fibular hypoplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the fibula. (Human Phenotype Ontology, HP_0003038)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003038
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Genes

13 genes associated with the fibular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
ATR ATR serine/threonine kinase
COL11A1 collagen, type XI, alpha 1
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
EIF4A3 eukaryotic translation initiation factor 4A3
FLNA filamin A, alpha
GDF5 growth differentiation factor 5
GPC6 glypican 6
IFT122 intraflagellar transport 122
SHOX short stature homeobox
SMOC1 SPARC related modular calcium binding 1
SOX9 SRY (sex determining region Y)-box 9
ZBTB16 zinc finger and BTB domain containing 16