abnormal compact bone lamellar structure Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the concentric layers of calcified matrix interspersed with osteocytes lodged in lacunae between the lamellae that comprise the cylindrical osteons (Mammalian Phenotype Ontology, MP_0010970)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010970
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Genes

4 gene mutations causing the abnormal compact bone lamellar structure 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
CSF1R colony stimulating factor 1 receptor
IGF2 insulin-like growth factor 2