ankyloglossia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Short or anteriorly attached lingual frenulum, associated with limited mobility of the tongue. (Human Phenotype Ontology, HP_0010296)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010296
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Genes

10 genes associated with the ankyloglossia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BCR breakpoint cluster region
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
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