Cartilaginous Exostosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0029423
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Genes

44 genes associated with the disease Cartilaginous Exostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
ARR3 arrestin 3, retinal (X-arrestin)
BCL2 B-cell CLL/lymphoma 2
BGLAP bone gamma-carboxyglutamate (gla) protein
BMP2 bone morphogenetic protein 2
CASR calcium-sensing receptor
CD274 CD274 molecule
CHP1 calcineurin-like EF-hand protein 1
CLCN5 chloride channel, voltage-sensitive 5
COX2
CXADR coxsackie virus and adenovirus receptor
DCTN3 dynactin 3 (p22)
DISC1 disrupted in schizophrenia 1
DYNC1H1 dynein, cytoplasmic 1, heavy chain 1
EXT1 exostosin glycosyltransferase 1
EXT2 exostosin glycosyltransferase 2
FGF9 fibroblast growth factor 9
FGFR3 fibroblast growth factor receptor 3
FN1 fibronectin 1
GLI3 GLI family zinc finger 3
GPC3 glypican 3
HDAC4 histone deacetylase 4
HPSE heparanase
HSPG2 heparan sulfate proteoglycan 2
IHH indian hedgehog
KAT6B K(lysine) acetyltransferase 6B
KCNH1 potassium channel, voltage gated eag related subfamily H, member 1
KIAA0195 KIAA0195
NPRL2 nitrogen permease regulator-like 2 (S. cerevisiae)
NR1I3 nuclear receptor subfamily 1, group I, member 3
PCNA proliferating cell nuclear antigen
PHB2 prohibitin 2
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PROM1 prominin 1
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
PTHLH parathyroid hormone-like hormone
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RARG retinoic acid receptor, gamma
SDC2 syndecan 2
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
SPON1 spondin 1, extracellular matrix protein
SPP1 secreted phosphoprotein 1
THEM4 thioesterase superfamily member 4
TRIM13 tripartite motif containing 13