abnormality of the labia majora Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the outer labia. (Human Phenotype Ontology, HP_0012881)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012881
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14 genes associated with the abnormality of the labia majora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GALTL beta 1,3-galactosyltransferase-like
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
FGFR2 fibroblast growth factor receptor 2
IRF6 interferon regulatory factor 6
NIPBL Nipped-B homolog (Drosophila)
ORC1 origin recognition complex, subunit 1
ORC4 origin recognition complex, subunit 4
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic)
RIPK4 receptor-interacting serine-threonine kinase 4
ROR2 receptor tyrosine kinase-like orphan receptor 2
SETBP1 SET binding protein 1
TP63 tumor protein p63
UBE3B ubiquitin protein ligase E3B
WNT5A wingless-type MMTV integration site family, member 5A