abnormal bone marrow development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the formation of the soft, pulpy tissue filling the medullary cavities of bones (Mammalian Phenotype Ontology, MP_0000168)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000168
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Genes

7 gene mutations causing the abnormal bone marrow development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CASP3 caspase 3, apoptosis-related cysteine peptidase
GSTA4 glutathione S-transferase alpha 4
IL6ST interleukin 6 signal transducer
KHDRBS1 KH domain containing, RNA binding, signal transduction associated 1
MZF1 myeloid zinc finger 1
NLK nemo-like kinase
PPARG peroxisome proliferator-activated receptor gamma