abnormal spleen primary b follicle morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the nodules of small undifferentiated B lymphocytes and follicular dendritic cells located in the spleen white pulp (Mammalian Phenotype Ontology, MP_0008471)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008471
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Genes

7 gene mutations causing the abnormal spleen primary b follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CXCR5 chemokine (C-X-C motif) receptor 5
IFNB1 interferon, beta 1, fibroblast
MAP3K14 mitogen-activated protein kinase kinase kinase 14
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
NKX2-3 NK2 homeobox 3
TNF tumor necrosis factor
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B