abnormality of the labia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the labia, the externally visible portions of the vulva. (Human Phenotype Ontology, HP_0000058)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000058
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Genes

26 genes associated with the abnormality of the labia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
ATIC 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase
B3GALTL beta 1,3-galactosyltransferase-like
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CHD7 chromodomain helicase DNA binding protein 7
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FGFR2 fibroblast growth factor receptor 2
IRF6 interferon regulatory factor 6
KAT6B K(lysine) acetyltransferase 6B
LMNA lamin A/C
NDN necdin, melanoma antigen (MAGE) family member
NIPBL Nipped-B homolog (Drosophila)
ORC1 origin recognition complex, subunit 1
ORC4 origin recognition complex, subunit 4
POR P450 (cytochrome) oxidoreductase
PORCN porcupine homolog (Drosophila)
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic)
RIPK4 receptor-interacting serine-threonine kinase 4
ROR2 receptor tyrosine kinase-like orphan receptor 2
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SETBP1 SET binding protein 1
SNRPN small nuclear ribonucleoprotein polypeptide N
TP63 tumor protein p63
UBE3B ubiquitin protein ligase E3B
WNT5A wingless-type MMTV integration site family, member 5A