abnormality of oral frenula Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the lingual frenulum, that is of the small fold of mucous membrane that attaches the tongue to the floor of the mouth, or the presence of accessory frenula in the oral cavity. (Human Phenotype Ontology, HP_0000190)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000190
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Genes

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

Symbol Name
B3GALTL beta 1,3-galactosyltransferase-like
BCR breakpoint cluster region
CD96 CD96 molecule
COL7A1 collagen, type VII, alpha 1
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
FAM111A family with sequence similarity 111, member A
FERMT1 fermitin family member 1
FLNA filamin A, alpha
IMPAD1 inositol monophosphatase domain containing 1
MAPK1 mitogen-activated protein kinase 1
MMP1 matrix metallopeptidase 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
TBX22 T-box 22
TCTN3 tectonic family member 3