Ankyloglossia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Short or anteriorly attached lingual frenulum, associated with limited mobility of the tongue. (Human Phenotype Ontology, HP_0010296)
External Link https://www.disgenet.org/browser/0/1/0/C0152415
Similar Terms
Downloads & Tools

Genes

19 genes associated with the disease Ankyloglossia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BCR breakpoint cluster region
COL7A1 collagen, type VII, alpha 1
CPOX coproporphyrinogen oxidase
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
EBP emopamil binding protein (sterol isomerase)
ETS1 v-ets avian erythroblastosis virus E26 oncogene homolog 1
FAM111A family with sequence similarity 111, member A
KMT2A lysine (K)-specific methyltransferase 2A
LAMA3 laminin, alpha 3
LAMB3 laminin, beta 3
LAMC2 laminin, gamma 2
LGR5 leucine-rich repeat containing G protein-coupled receptor 5
MAPK1 mitogen-activated protein kinase 1
MIPEP mitochondrial intermediate peptidase
MMP1 matrix metallopeptidase 1
NXN nucleoredoxin
ROR2 receptor tyrosine kinase-like orphan receptor 2
RSPO2 R-spondin 2
TBX22 T-box 22