abnormal lymph node medulla morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the area of the lymph node through which lymph leaves the node; it contains macrophages and antibody-secreting plasma cells (Mammalian Phenotype Ontology, MP_0002348)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002348
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Genes

9 gene mutations causing the abnormal lymph node medulla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CTSV cathepsin V
CXCR2 chemokine (C-X-C motif) receptor 2
FOXP3 forkhead box P3
FZD9 frizzled class receptor 9
HR hair growth associated
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL10RB interleukin 10 receptor, beta