hypoplasia of dental enamel Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Developmental hypoplasia of the dental enamel. (Human Phenotype Ontology, HP_0006297)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006297
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Genes

35 genes associated with the hypoplasia of dental enamel phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIRE autoimmune regulator
ALDH3A2 aldehyde dehydrogenase 3 family, member A2
ATR ATR serine/threonine kinase
CLDN1 claudin 1
COG6 component of oligomeric golgi complex 6
COL7A1 collagen, type VII, alpha 1
CREBBP CREB binding protein
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
ERCC4 excision repair cross-complementation group 4
FAM20C family with sequence similarity 20, member C
FGF10 fibroblast growth factor 10
FGF23 fibroblast growth factor 23
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FLNB filamin B, beta
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
GJA1 gap junction protein, alpha 1, 43kDa
GNAS GNAS complex locus
IFT122 intraflagellar transport 122
ITGA6 integrin, alpha 6
ITGB4 integrin, beta 4
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
KL klotho
LAMA3 laminin, alpha 3
LAMB3 laminin, beta 3
LAMC2 laminin, gamma 2
OCRL oculocerebrorenal syndrome of Lowe
OFD1 oral-facial-digital syndrome 1
PCNT pericentrin
PLEC plectin
PORCN porcupine homolog (Drosophila)
PVRL4 poliovirus receptor-related 4
ROGDI rogdi homolog (Drosophila)
RUNX2 runt-related transcription factor 2
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor