osteosclerosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A bone remodeling disease that results_in abnormal elevated bone density or mass. (Human Disease Ontology, DOID_4254)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005422
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Genes

11 gene mutations causing the osteosclerosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
CSF1 colony stimulating factor 1 (macrophage)
FAM20C family with sequence similarity 20, member C
GUSB glucuronidase, beta
HIVEP3 human immunodeficiency virus type I enhancer binding protein 3
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LRRK1 leucine-rich repeat kinase 1
LTBP3 latent transforming growth factor beta binding protein 3
MITF microphthalmia-associated transcription factor
NCOR2 nuclear receptor corepressor 2
THRA thyroid hormone receptor, alpha