split foot Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A condition in which middle parts of the foot (toes and metatarsals) are missing giving a cleft appearance. The severity is very variable ranging from slightly hypoplastic 3rd toe over absent 2nd or 3rd toes as far as oligo- or monodactyl feet. (Human Phenotype Ontology, HP_0001839)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001839
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Genes

9 genes associated with the split foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DLX5 distal-less homeobox 5
FGFR2 fibroblast growth factor receptor 2
LRP4 low density lipoprotein receptor-related protein 4
PORCN porcupine homolog (Drosophila)
SALL1 spalt-like transcription factor 1
SNX3 sorting nexin 3
TP63 tumor protein p63
WNT10B wingless-type MMTV integration site family, member 10B
WNT7A wingless-type MMTV integration site family, member 7A