failure of secondary bone resorption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description inability to degrade the organic and inorganic phases of bone by absorption, usually by the abnormal function or by absence of osteoclasts (Mammalian Phenotype Ontology, MP_0000064)
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5 gene mutations causing the failure of secondary bone resorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
COL1A1 collagen, type I, alpha 1
CSF1R colony stimulating factor 1 receptor
LECT1 leukocyte cell derived chemotaxin 1
OSTM1 osteopetrosis associated transmembrane protein 1
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3