increased trabecular bone thickness Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description thicker than normal bone with a lattice-like or spongy structure (Mammalian Phenotype Ontology, MP_0009347)
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32 gene mutations causing the increased trabecular bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABHD5 abhydrolase domain containing 5
AGER advanced glycosylation end product-specific receptor
AGTR2 angiotensin II receptor, type 2
AMPD3 adenosine monophosphate deaminase 3
BGLAP bone gamma-carboxyglutamate (gla) protein
CAV1 caveolin 1, caveolae protein, 22kDa
CCR2 chemokine (C-C motif) receptor 2
CD47 CD47 molecule
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CHAD chondroadherin
CLCN7 chloride channel, voltage-sensitive 7
EBF1 early B-cell factor 1
FAM107B family with sequence similarity 107, member B
HIVEP3 human immunodeficiency virus type I enhancer binding protein 3
HTRA1 HtrA serine peptidase 1
IL20RA interleukin 20 receptor, alpha
IL6ST interleukin 6 signal transducer
INPP4B inositol polyphosphate-4-phosphatase, type II, 105kDa
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LRRK1 leucine-rich repeat kinase 1
NOS1 nitric oxide synthase 1 (neuronal)
NPY2R neuropeptide Y receptor Y2
PGR progesterone receptor
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific)
SBNO2 strawberry notch homolog 2 (Drosophila)
SNAPC4 small nuclear RNA activating complex, polypeptide 4, 190kDa
SOST sclerostin
SPP1 secreted phosphoprotein 1
THRA thyroid hormone receptor, alpha
TMEM64 transmembrane protein 64
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator
XYLT1 xylosyltransferase I