decreased bone strength Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced ability of bone to endure the application of force without yielding or breaking (Mammalian Phenotype Ontology, MP_0004991)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004991
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Genes

20 gene mutations causing the decreased bone strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BBX bobby sox homolog (Drosophila)
CADM1 cell adhesion molecule 1
CALCB calcitonin-related polypeptide beta
CHAD chondroadherin
CLDN18 claudin 18
COL12A1 collagen, type XII, alpha 1
COL1A2 collagen, type I, alpha 2
CSF1R colony stimulating factor 1 receptor
EBF2 early B-cell factor 2
ESR1 estrogen receptor 1
FAM73B family with sequence similarity 73, member B
FZD9 frizzled class receptor 9
GJA1 gap junction protein, alpha 1, 43kDa
ID1 inhibitor of DNA binding 1, dominant negative helix-loop-helix protein
IL10 interleukin 10
INPP5D inositol polyphosphate-5-phosphatase, 145kDa
ISG15 ISG15 ubiquitin-like modifier
KLF10 Kruppel-like factor 10
NCOR2 nuclear receptor corepressor 2
WNT16 wingless-type MMTV integration site family, member 16