increased bone resorption Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Osteolysis refers to the destruction of bone through bone resorption with removal or loss of calcium. (Human Phenotype Ontology, HP_0002797)
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19 gene mutations causing the increased bone resorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CLDN18 claudin 18
CNOT3 CCR4-NOT transcription complex, subunit 3
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
FOSL2 FOS-like antigen 2
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GSK3B glycogen synthase kinase 3 beta
IAPP islet amyloid polypeptide
IL1B interleukin 1, beta
IL1R1 interleukin 1 receptor, type I
INPP4B inositol polyphosphate-4-phosphatase, type II, 105kDa
LIF leukemia inhibitory factor
NCOA1 nuclear receptor coactivator 1
NLRP3 NLR family, pyrin domain containing 3
STAT1 signal transducer and activator of transcription 1, 91kDa
TOB2 transducer of ERBB2, 2
USP1 ubiquitin specific peptidase 1
WWOX WW domain containing oxidoreductase