adactyly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The absence of all phalanges of all the digits of a limb and the associated soft tissues. (Human Phenotype Ontology, HP_0009776)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009776
Similar Terms
Downloads & Tools

Genes

11 genes associated with the adactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARHGAP31 Rho GTPase activating protein 31
BMPR1B bone morphogenetic protein receptor, type IB
DOCK6 dedicator of cytokinesis 6
DOLK dolichol kinase
EOGT EGF domain-specific O-linked N-acetylglucosamine (GlcNAc) transferase
FIG4 FIG4 phosphoinositide 5-phosphatase
GDF5 growth differentiation factor 5
NOTCH1 notch 1
PIGL phosphatidylinositol glycan anchor biosynthesis, class L
RBPJ recombination signal binding protein for immunoglobulin kappa J region
WNT7A wingless-type MMTV integration site family, member 7A