abnormal compact bone area Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the total amount of cross-sectional area of compact bone tissue (Mammalian Phenotype Ontology, MP_0010966)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010966
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17 gene mutations causing the abnormal compact bone area phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANKRD11 ankyrin repeat domain 11
CAV1 caveolin 1, caveolae protein, 22kDa
COL1A2 collagen, type I, alpha 2
CTSK cathepsin K
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
KLF10 Kruppel-like factor 10
NLRP3 NLR family, pyrin domain containing 3
P2RY13 purinergic receptor P2Y, G-protein coupled, 13
PCOLCE procollagen C-endopeptidase enhancer
PDIA3 protein disulfide isomerase family A, member 3
SIGLEC15 sialic acid binding Ig-like lectin 15
SOST sclerostin
THRA thyroid hormone receptor, alpha
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator
WNT16 wingless-type MMTV integration site family, member 16
WWOX WW domain containing oxidoreductase