aplasia/hypoplasia of the fibula Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the fibula. (Human Phenotype Ontology, HP_0006492)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006492
Similar Terms
Downloads & Tools

Genes

19 genes associated with the aplasia/hypoplasia of the fibula 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
BMPR1B bone morphogenetic protein receptor, type IB
COL11A1 collagen, type XI, alpha 1
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
EIF4A3 eukaryotic translation initiation factor 4A3
FLNA filamin A, alpha
FLNB filamin B, beta
GDF5 growth differentiation factor 5
GPC6 glypican 6
IFT122 intraflagellar transport 122
LMBR1 limb development membrane protein 1
RBM8A RNA binding motif protein 8A
SHOX short stature homeobox
SMOC1 SPARC related modular calcium binding 1
SOX9 SRY (sex determining region Y)-box 9
TBX15 T-box 15
WNT7A wingless-type MMTV integration site family, member 7A
ZBTB16 zinc finger and BTB domain containing 16