abnormal trabecular bone mass Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the total amount of trabecular bone tissue contained in the skeleton (Mammalian Phenotype Ontology, MP_0010871)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010871
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Genes

27 gene mutations causing the abnormal trabecular bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CD40 CD40 molecule, TNF receptor superfamily member 5
CD40LG CD40 ligand
CNOT3 CCR4-NOT transcription complex, subunit 3
CSF1 colony stimulating factor 1 (macrophage)
CTHRC1 collagen triple helix repeat containing 1
CTSK cathepsin K
DCSTAMP dendrocyte expressed seven transmembrane protein
GAB2 GRB2-associated binding protein 2
GSK3B glycogen synthase kinase 3 beta
IL10 interleukin 10
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
LRP5 low density lipoprotein receptor-related protein 5
LTBP3 latent transforming growth factor beta binding protein 3
MGP matrix Gla protein
MMP13 matrix metallopeptidase 13
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NLRP3 NLR family, pyrin domain containing 3
PKD1 polycystic kidney disease 1 (autosomal dominant)
PLXNA1 plexin A1
PPARG peroxisome proliferator-activated receptor gamma
SIGLEC15 sialic acid binding Ig-like lectin 15
SMURF1 SMAD specific E3 ubiquitin protein ligase 1
SRC SRC proto-oncogene, non-receptor tyrosine kinase
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
TOB1 transducer of ERBB2, 1
TYROBP TYRO protein tyrosine kinase binding protein