oligodactyly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect resulting in the presence of fewer than the normal number of digits. (Human Phenotype Ontology, HP_0012165)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012165
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
CYP26B1 cytochrome P450, family 26, subfamily B, polypeptide 1
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
GLI3 GLI family zinc finger 3
NIPBL Nipped-B homolog (Drosophila)
PORCN porcupine homolog (Drosophila)
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SF3B4 splicing factor 3b, subunit 4, 49kDa
SMOC1 SPARC related modular calcium binding 1
WNT10B wingless-type MMTV integration site family, member 10B
WNT7A wingless-type MMTV integration site family, member 7A