abnormal bone marrow cavity morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the medullary cavities of the bones (Mammalian Phenotype Ontology, MP_0000065)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000065
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Genes

18 gene mutations causing the abnormal bone marrow cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACKR1 atypical chemokine receptor 1 (Duffy blood group)
CLCN7 chloride channel, voltage-sensitive 7
COL11A1 collagen, type XI, alpha 1
COL2A1 collagen, type II, alpha 1
CSF1 colony stimulating factor 1 (macrophage)
CTSK cathepsin K
FOS FBJ murine osteosarcoma viral oncogene homolog
HIVEP3 human immunodeficiency virus type I enhancer binding protein 3
HSPG2 heparan sulfate proteoglycan 2
IGF2 insulin-like growth factor 2
LRRK1 leucine-rich repeat kinase 1
NCOR2 nuclear receptor corepressor 2
NLRP3 NLR family, pyrin domain containing 3
PKD1 polycystic kidney disease 1 (autosomal dominant)
RUNX2 runt-related transcription factor 2
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
SRC SRC proto-oncogene, non-receptor tyrosine kinase
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3