median cleft lip Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of cleft lip presenting as a midline (median) gap in the upper lip. (Human Phenotype Ontology, HP_0000161)
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17 genes associated with the median cleft lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALX3 ALX homeobox 3
DDX59 DEAD (Asp-Glu-Ala-Asp) box polypeptide 59
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
GJA1 gap junction protein, alpha 1, 43kDa
HYLS1 hydrolethalus syndrome 1
IFT80 intraflagellar transport 80
NEK1 NIMA-related kinase 1
OFD1 oral-facial-digital syndrome 1
PTCH1 patched 1
RIPK4 receptor-interacting serine-threonine kinase 4
SIX3 SIX homeobox 3
SNX3 sorting nexin 3
TCTN3 tectonic family member 3
TGIF1 TGFB-induced factor homeobox 1
WDR34 WD repeat domain 34
WDR35 WD repeat domain 35
WDR60 WD repeat domain 60