abnormal osteocyte morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of a mature osteoblast that has become embedded in the bone matrix (osteoid) in small cavities called lacuna and is connected to adjacent osteocytes via protoplasmic projections called canaliculi (Mammalian Phenotype Ontology, MP_0008753)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008753
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12 gene mutations causing the abnormal osteocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
CSF1 colony stimulating factor 1 (macrophage)
CSF1R colony stimulating factor 1 receptor
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
KLF10 Kruppel-like factor 10
NACA nascent polypeptide-associated complex alpha subunit
PHEX phosphate regulating endopeptidase homolog, X-linked
PTH parathyroid hormone
PTHLH parathyroid hormone-like hormone
SOST sclerostin
SUCO SUN domain containing ossification factor