impaired osteoblast differentiation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced ability or inability to produce skeletogenic cells that secrete osteoid, are capable of producing mineralized (hydroxyapatite) matrix, are located adjacent to or within osteoid tissue, and arise from the transformation of a preosteoblast cell (Mammalian Phenotype Ontology, MP_0011711)
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5 gene mutations causing the impaired osteoblast differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EVC2 Ellis van Creveld syndrome 2
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
MMP14 matrix metallopeptidase 14 (membrane-inserted)
SBNO2 strawberry notch homolog 2 (Drosophila)
TMEM119 transmembrane protein 119