Osteofibrous Dysplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1709353
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Genes

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

Symbol Name
AMPH amphiphysin
B3GAT1 beta-1,3-glucuronyltransferase 1
BGLAP bone gamma-carboxyglutamate (gla) protein
C2CD3 C2 calcium-dependent domain containing 3
C5ORF42 chromosome 5 open reading frame 42
CENPJ centromere protein J
CEP120 centrosomal protein 120kDa
DLEU7 deleted in lymphocytic leukemia, 7
DRD3 dopamine receptor D3
GHR growth hormone receptor
GNAS GNAS complex locus
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
INTU inturned planar cell polarity protein
KIAA0753 KIAA0753
MET MET proto-oncogene, receptor tyrosine kinase
NF1 neurofibromin 1
OFD1 oral-facial-digital syndrome 1
S100A1 S100 calcium binding protein A1
S100B S100 calcium binding protein B
SCLT1 sodium channel and clathrin linker 1
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TBC1D32 TBC1 domain family, member 32
TCTN3 tectonic family member 3
TMEM107 transmembrane protein 107
TMEM216 transmembrane protein 216