Maxillary Diseases Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

5 genes associated with the Maxillary Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
CALCR calcitonin receptor
CYP2C8 cytochrome P450, family 2, subfamily C, polypeptide 8
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
IL1A interleukin 1, alpha
IL1B interleukin 1, beta