Hypochondroplasia (Disorder) Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0410529
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Genes

16 genes associated with the disease Hypochondroplasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
BGLAP bone gamma-carboxyglutamate (gla) protein
BUD13 BUD13 homolog (S. cerevisiae)
DOCK7 dedicator of cytokinesis 7
FGF3 fibroblast growth factor 3
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GALNT2 polypeptide N-acetylgalactosaminyltransferase 2
GH1 growth hormone 1
IGF1 insulin-like growth factor 1 (somatomedin C)
LDLR low density lipoprotein receptor
NPPC natriuretic peptide C
PCSK9 proprotein convertase subtilisin/kexin type 9
SHOX short stature homeobox
ZPR1 ZPR1 zinc finger