increased osteochondroma incidence Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the expected number of a benign cartilagenous neoplasm that consists of a pedicle of normal bone capped by a region of proliferating cartilage cells, occurring in a specific population in a given time period; osteochondroma is most often associated with one or more of the long bones (Mammalian Phenotype Ontology, MP_0010079)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010079
Similar Terms
Downloads & Tools

Genes

2 gene mutations causing the increased osteochondroma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR1 activin A receptor, type I
EXT1 exostosin glycosyltransferase 1