| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A bone inflammation disease that results_from infection located_in bone and located_in bone marrow. (Experimental Factor Ontology, EFO_0003102) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005190 |
| Similar Terms | |
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6 gene mutations causing the osteomyelitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| CEBPE | CCAAT/enhancer binding protein (C/EBP), epsilon |
| ENPP1 | ectonucleotide pyrophosphatase/phosphodiesterase 1 |
| IL1R1 | interleukin 1 receptor, type I |
| NLRP3 | NLR family, pyrin domain containing 3 |
| PSTPIP2 | proline-serine-threonine phosphatase interacting protein 2 |
| SH3BP2 | SH3-domain binding protein 2 |
