labial hypoplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000066
Similar Terms
Downloads & Tools

Genes

19 genes associated with the labial hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GALTL beta 1,3-galactosyltransferase-like
CHD7 chromodomain helicase DNA binding protein 7
FGFR2 fibroblast growth factor receptor 2
IRF6 interferon regulatory factor 6
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