broad hallux Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Visible increase in width of the hallux without an increase in the dorso-ventral dimension. (Human Phenotype Ontology, HP_0010055)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010055
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Genes

21 genes associated with the broad hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
BMP2 bone morphogenetic protein 2
BMPR1B bone morphogenetic protein receptor, type IB
CREBBP CREB binding protein
EFNB1 ephrin-B1
EP300 E1A binding protein p300
FGF10 fibroblast growth factor 10
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FLNA filamin A, alpha
GDF5 growth differentiation factor 5
GLI3 GLI family zinc finger 3
MED12 mediator complex subunit 12
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NOG noggin
NPR2 natriuretic peptide receptor 2
SF3B4 splicing factor 3b, subunit 4, 49kDa
SUMF1 sulfatase modifying factor 1
TWIST1 twist family bHLH transcription factor 1
UBE2A ubiquitin-conjugating enzyme E2A