postaxial foot polydactyly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Polydactyly of the foot most commonly refers to the presence of six toes on one foot. Postaxial polydactyly affects the lateral ray and the duplication may range from a well-formed articulated digit to a rudimentary digit. (Human Phenotype Ontology, HP_0001830)
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37 genes associated with the postaxial foot polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B9D1 B9 protein domain 1
B9D2 B9 protein domain 2
BMP4 bone morphogenetic protein 4
CC2D2A coiled-coil and C2 domain containing 2A
CD96 CD96 molecule
CEP290 centrosomal protein 290kDa
DDX59 DEAD (Asp-Glu-Ala-Asp) box polypeptide 59
DHCR7 7-dehydrocholesterol reductase
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
EVC Ellis van Creveld protein
EVC2 Ellis van Creveld syndrome 2
FNBP4 formin binding protein 4
GLI3 GLI family zinc finger 3
HOXD13 homeobox D13
IFT140 intraflagellar transport 140
IFT172 intraflagellar transport 172
IFT80 intraflagellar transport 80
KIF7 kinesin family member 7
LBR lamin B receptor
LMBR1 limb development membrane protein 1
MKKS McKusick-Kaufman syndrome
MKS1 Meckel syndrome, type 1
NEK1 NIMA-related kinase 1
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
SC5D sterol-C5-desaturase
SHH sonic hedgehog
SMOC1 SPARC related modular calcium binding 1
TCTN2 tectonic family member 2
TMEM216 transmembrane protein 216
TMEM231 transmembrane protein 231
TMEM67 transmembrane protein 67
TTC21B tetratricopeptide repeat domain 21B
WDPCP WD repeat containing planar cell polarity effector
WDR19 WD repeat domain 19
WDR34 WD repeat domain 34
WDR60 WD repeat domain 60