abnormal compact bone mass Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the total amount of compact bone tissue contained in the skeleton (Mammalian Phenotype Ontology, MP_0010960)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010960
Similar Terms
Downloads & Tools


10 gene mutations causing the abnormal compact bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CD40 CD40 molecule, TNF receptor superfamily member 5
CD40LG CD40 ligand
GAB2 GRB2-associated binding protein 2
GSK3B glycogen synthase kinase 3 beta
IL10 interleukin 10
LRP5 low density lipoprotein receptor-related protein 5
MGP matrix Gla protein
NFE2 nuclear factor, erythroid 2
NOS2 nitric oxide synthase 2, inducible
PKD1 polycystic kidney disease 1 (autosomal dominant)