decreased compact bone area Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduction in the total amount of cross-sectional area of compact bone tissue (Mammalian Phenotype Ontology, MP_0010968)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010968
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Genes

9 gene mutations causing the decreased compact bone area phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANKRD11 ankyrin repeat domain 11
COL1A2 collagen, type I, alpha 2
ESR1 estrogen receptor 1
KLF10 Kruppel-like factor 10
NLRP3 NLR family, pyrin domain containing 3
PDIA3 protein disulfide isomerase family A, member 3
THRA thyroid hormone receptor, alpha
WNT16 wingless-type MMTV integration site family, member 16
WWOX WW domain containing oxidoreductase