Dentin Dysplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A teeth hard tissue disease characterized by presence of normal enamel but atypical dentin with abnormal pulpal morphology. (Human Disease Ontology, DOID_701)
External Link https://www.disgenet.org/browser/0/1/0/C0011430
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Genes

19 genes associated with the disease Dentin Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
AKR1C1 aldo-keto reductase family 1, member C1
AKR1C2 aldo-keto reductase family 1, member C2
ALPL alkaline phosphatase, liver/bone/kidney
AMELY amelogenin, Y-linked
CDH11 cadherin 11, type 2, OB-cadherin (osteoblast)
DSPP dentin sialophosphoprotein
ENAM enamelin
MMP20 matrix metallopeptidase 20
NET1 neuroepithelial cell transforming 1
PRPF38B pre-mRNA processing factor 38B
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 5
SMOC2 SPARC related modular calcium binding 2
SPP1 secreted phosphoprotein 1
SSUH2 ssu-2 homolog (C. elegans)
TSPAN1 tetraspanin 1
VPS4B vacuolar protein sorting 4 homolog B (S. cerevisiae)
WDR72 WD repeat domain 72