Accessory Oral Frenulum Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Extra fold of tissue extending from the alveolar ridge to the inner surface of the upper or lower lip. (Human Phenotype Ontology, HP_0000191)
External Link https://www.disgenet.org/browser/0/1/0/C4021814
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Genes

12 genes associated with the disease Accessory Oral Frenulum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ASXL1 additional sex combs like transcriptional regulator 1
C5ORF42 chromosome 5 open reading frame 42
CD96 CD96 molecule
DDX59 DEAD (Asp-Glu-Ala-Asp) box polypeptide 59
DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1
EFTUD2 elongation factor Tu GTP binding domain containing 2
GLI3 GLI family zinc finger 3
IFT140 intraflagellar transport 140
IFT57 intraflagellar transport 57
KLHL7 kelch-like family member 7
OFD1 oral-facial-digital syndrome 1
TCTN3 tectonic family member 3