increased bone mineral content Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description elevation in the amount (usually in grams/cm) of bone mineral divided by a bone-scanned area (Mammalian Phenotype Ontology, MP_0010123)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010123
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Genes

38 gene mutations causing the increased bone mineral content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
AGER advanced glycosylation end product-specific receptor
AHCYL1 adenosylhomocysteinase-like 1
ANKH ANKH inorganic pyrophosphate transport regulator
B9D1 B9 protein domain 1
CBX6 chromobox homolog 6
CD14 CD14 molecule
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
DSG1 desmoglein 1
EPB41L5 erythrocyte membrane protein band 4.1 like 5
FGF23 fibroblast growth factor 23
FKBP11 FK506 binding protein 11, 19 kDa
FRZB frizzled-related protein
HDAC6 histone deacetylase 6
IL6ST interleukin 6 signal transducer
KLKB1 kallikrein B, plasma (Fletcher factor) 1
L3MBTL2 l(3)mbt-like 2 (Drosophila)
METTL24 methyltransferase like 24
MSTN myostatin
NOS1 nitric oxide synthase 1 (neuronal)
NPTN neuroplastin
PDYN prodynorphin
PTPN3 protein tyrosine phosphatase, non-receptor type 3
PYY peptide YY
RNF7 ring finger protein 7
SECISBP2 SECIS binding protein 2
SETDB1 SET domain, bifurcated 1
SIGLEC15 sialic acid binding Ig-like lectin 15
SNAP47 synaptosomal-associated protein, 47kDa
SPNS2 spinster homolog 2 (Drosophila)
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TLR4 toll-like receptor 4
TMEM64 transmembrane protein 64
TNFAIP1 tumor necrosis factor, alpha-induced protein 1 (endothelial)
TYROBP TYRO protein tyrosine kinase binding protein
USH1C Usher syndrome 1C (autosomal recessive, severe)
WDR37 WD repeat domain 37
XYLB xylulokinase homolog (H. influenzae)