abnormality of the mandible Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the mandible, the bone of the lower jaw. (Human Phenotype Ontology, HP_0000277)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0000277
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Genes

17 genes associated with the abnormality of the mandible phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
TSPAN9 tetraspanin 9 0.868241
MRC2 mannose receptor, C type 2 0.809986
APOL3 apolipoprotein L, 3 0.809986
PCSK5 proprotein convertase subtilisin/kexin type 5 0.772842
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 0.757258
ZNF618 zinc finger protein 618 0.718314
ULK4 unc-51 like kinase 4 0.690584
RHPN2 rhophilin, Rho GTPase binding protein 2 0.664442
THRB thyroid hormone receptor, beta 0.664442
FRMD4A FERM domain containing 4A 0.654304
LOC100506274 uncharacterized LOC100506274 0.60762
OXR1 oxidation resistance 1 0.60762
N4BP1 NEDD4 binding protein 1 0.60762
CCDC81 coiled-coil domain containing 81 0.597506
EXT2 exostosin glycosyltransferase 2 0.591289
FSTL4 follistatin-like 4 0.585507
APP amyloid beta (A4) precursor protein 0.577224