Median Cleft Lip Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of cleft lip presenting as a midline (median) gap in the upper lip. (Human Phenotype Ontology, HP_0000161)
External Link https://www.disgenet.org/browser/0/1/0/C1850256
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Genes

15 genes associated with the disease Median Cleft Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALX3 ALX homeobox 3
CELSR2 cadherin, EGF LAG seven-pass G-type receptor 2
DDX59 DEAD (Asp-Glu-Ala-Asp) box polypeptide 59
GJA1 gap junction protein, alpha 1, 43kDa
GLI3 GLI family zinc finger 3
HYLS1 hydrolethalus syndrome 1
INTU inturned planar cell polarity protein
NEK1 NIMA-related kinase 1
OFD1 oral-facial-digital syndrome 1
PIGN phosphatidylinositol glycan anchor biosynthesis, class N
RIPK4 receptor-interacting serine-threonine kinase 4
TCTN3 tectonic family member 3
TGIF1 TGFB-induced factor homeobox 1
TMCO1 transmembrane and coiled-coil domains 1
ZSWIM6 zinc finger, SWIM-type containing 6