Mouth Abnormalities Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the oral cavity (Mammalian Phenotype Ontology, MP_0000452)
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24 genes associated with the Mouth Abnormalities phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ADH1C alcohol dehydrogenase 1C (class I), gamma polypeptide
ADTRP androgen-dependent TFPI-regulating protein
ALX4 ALX homeobox 4
APEX1 APEX nuclease (multifunctional DNA repair enzyme) 1
BHMT betaine--homocysteine S-methyltransferase
BHMT2 betaine--homocysteine S-methyltransferase 2
CD44 CD44 molecule (Indian blood group)
CRHR1 corticotropin releasing hormone receptor 1
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
ERCC2 excision repair cross-complementation group 2
GLI3 GLI family zinc finger 3
HDAC4 histone deacetylase 4
LEF1 lymphoid enhancer-binding factor 1
MAPT microtubule-associated protein tau
MLPH melanophilin
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
OGG1 8-oxoguanine DNA glycosylase
SCN3B sodium channel, voltage gated, type III beta subunit
SP100 SP100 nuclear antigen
SPPL2C signal peptide peptidase like 2C
XRCC1 X-ray repair complementing defective repair in Chinese hamster cells 1
XRCC3 X-ray repair complementing defective repair in Chinese hamster cells 3
ZNF202 zinc finger protein 202