abnormal ossification involved in bone maturation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone, involved in the progression of the developing skeleton from its formation to its mature state (Mammalian Phenotype Ontology, MP_0011722)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011722
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1 gene mutations causing the abnormal ossification involved in bone maturation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PTPN2 protein tyrosine phosphatase, non-receptor type 2