increased compact bone thickness Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description thicker than normal superficial layer of compact bone (Mammalian Phenotype Ontology, MP_0004148)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004148
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Genes

27 gene mutations causing the increased compact bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADIPOQ adiponectin, C1Q and collagen domain containing
AGER advanced glycosylation end product-specific receptor
APOE apolipoprotein E
BGLAP bone gamma-carboxyglutamate (gla) protein
CLEC2D C-type lectin domain family 2, member D
COL2A1 collagen, type II, alpha 1
FRZB frizzled-related protein
GSK3B glycogen synthase kinase 3 beta
GSN gelsolin
HIVEP3 human immunodeficiency virus type I enhancer binding protein 3
HSPG2 heparan sulfate proteoglycan 2
IGF2 insulin-like growth factor 2
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LRRK1 leucine-rich repeat kinase 1
MSTN myostatin
NOS3 nitric oxide synthase 3 (endothelial cell)
NOV nephroblastoma overexpressed
PCOLCE procollagen C-endopeptidase enhancer
PGR progesterone receptor
PTH parathyroid hormone
PTHLH parathyroid hormone-like hormone
SMURF1 SMAD specific E3 ubiquitin protein ligase 1
SOST sclerostin
STAT1 signal transducer and activator of transcription 1, 91kDa
THBS2 thrombospondin 2
THRB thyroid hormone receptor, beta
VCP valosin containing protein