Developmental Absence Of Tooth Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0399352
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Genes

39 genes associated with the disease Developmental Absence Of Tooth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARHGAP15 Rho GTPase activating protein 15
BMP4 bone morphogenetic protein 4
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CALML3 calmodulin-like 3
CHD7 chromodomain helicase DNA binding protein 7
CHDH choline dehydrogenase
COTL1 coactosin-like F-actin binding protein 1
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
DCAF17 DDB1 and CUL4 associated factor 17
DVL1 dishevelled segment polarity protein 1
DVL3 dishevelled segment polarity protein 3
EDA ectodysplasin A
EDAR ectodysplasin A receptor
EDARADD EDAR-associated death domain
FGF17 fibroblast growth factor 17
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FLNA filamin A, alpha
FOXP1 forkhead box P1
FZD2 frizzled class receptor 2
IFT122 intraflagellar transport 122
IHH indian hedgehog
IRF6 interferon regulatory factor 6
IRX5 iroquois homeobox 5
KISS1R KISS1 receptor
LTBP3 latent transforming growth factor beta binding protein 3
MAPK14 mitogen-activated protein kinase 14
MBL2 mannose-binding lectin (protein C) 2, soluble
MSX1 msh homeobox 1
NECTIN1 nectin cell adhesion molecule 1
NOL11 nucleolar protein 11
OTOR otoraplin
PAX9 paired box 9
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
TGFA transforming growth factor, alpha
TNF tumor necrosis factor
UBXN11 UBX domain protein 11
WNT10A wingless-type MMTV integration site family, member 10A
WNT5A wingless-type MMTV integration site family, member 5A