aplasia/hypoplasia of the hallux Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the big toe. (Human Phenotype Ontology, HP_0008362)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008362
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Genes

16 genes associated with the aplasia/hypoplasia of the 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
ACVR1 activin A receptor, type I
BMP2 bone morphogenetic protein 2
BMPR1B bone morphogenetic protein receptor, type IB
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FIG4 FIG4 phosphoinositide 5-phosphatase
FLNA filamin A, alpha
GDF5 growth differentiation factor 5
GJA1 gap junction protein, alpha 1, 43kDa
HOXA13 homeobox A13
IHH indian hedgehog
KCNJ8 potassium channel, inwardly rectifying subfamily J, member 8
MGP matrix Gla protein
NOG noggin
SALL4 spalt-like transcription factor 4