Hypophosphatasia 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_14213)
External Link https://www.disgenet.org/browser/0/1/0/C0020630
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Genes

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

Symbol Name
ALDH7A1 aldehyde dehydrogenase 7 family, member A1
ALPL alkaline phosphatase, liver/bone/kidney
ALPP alkaline phosphatase, placental
ASRGL1 asparaginase like 1
ATRNL1 attractin-like 1
BGLAP bone gamma-carboxyglutamate (gla) protein
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CCL27 chemokine (C-C motif) ligand 27
CP ceruloplasmin (ferroxidase)
DLX3 distal-less homeobox 3
FGFR3 fibroblast growth factor receptor 3
LRP6 low density lipoprotein receptor-related protein 6
MYBPC1 myosin binding protein C, slow type
NAT10 N-acetyltransferase 10 (GCN5-related)
P2RX7 purinergic receptor P2X, ligand gated ion channel, 7
PDLIM3 PDZ and LIM domain 3
PDXP pyridoxal (pyridoxine, vitamin B6) phosphatase
PIGT phosphatidylinositol glycan anchor biosynthesis, class T
PLP1 proteolipid protein 1
PLPBP pyridoxal phosphate binding protein
PRDX5 peroxiredoxin 5
PTHLH parathyroid hormone-like hormone
RUNX2 runt-related transcription factor 2
SFTPB surfactant protein B
SLPI secretory leukocyte peptidase inhibitor
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11