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
Similar Terms
Downloads & Tools

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