Dentinogenesis Imperfecta Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_4154)
External Link https://www.disgenet.org/browser/0/1/0/C0011436
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Genes

35 genes associated with the disease Dentinogenesis Imperfecta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AKR1C2 aldo-keto reductase family 1, member C2
ALB albumin
AMELY amelogenin, Y-linked
BMP1 bone morphogenetic protein 1
BMP2 bone morphogenetic protein 2
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
CXCL10 chemokine (C-X-C motif) ligand 10
DLX3 distal-less homeobox 3
DMP1 dentin matrix acidic phosphoprotein 1
DMTF1 cyclin D binding myb-like transcription factor 1
DSG1 desmoglein 1
DSPP dentin sialophosphoprotein
ENAM enamelin
FKBP10 FK506 binding protein 10, 65 kDa
GC group-specific component (vitamin D binding protein)
GDF2 growth differentiation factor 2
IFNG interferon, gamma
KLK4 kallikrein-related peptidase 4
MMP20 matrix metallopeptidase 20
MMP9 matrix metallopeptidase 9
NET1 neuroepithelial cell transforming 1
PPIB peptidylprolyl isomerase B (cyclophilin B)
PRPF38B pre-mRNA processing factor 38B
SEC24D SEC24 family member D
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
SLC6A5 solute carrier family 6 (neurotransmitter transporter), member 5
SPP1 secreted phosphoprotein 1
TNC tenascin C
TNNC1 troponin C type 1 (slow)
TRIP11 thyroid hormone receptor interactor 11
TSPAN1 tetraspanin 1
WDR72 WD repeat domain 72
ZNF469 zinc finger protein 469