abnormal peyer's patch germinal center morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the area of the Peyer's patch where B cells proliferate and differentiate into plasma cells (Mammalian Phenotype Ontology, MP_0002391)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002391
Similar Terms
Downloads & Tools

Genes

17 gene mutations causing the abnormal peyer's patch germinal center morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BCL3 B-cell CLL/lymphoma 3
BCL6 B-cell CLL/lymphoma 6
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CCR6 chemokine (C-C motif) receptor 6
CYLD cylindromatosis (turban tumor syndrome)
FOXN1 forkhead box N1
ICOS inducible T-cell co-stimulator
IGKC immunoglobulin kappa constant
MIR155 microRNA 155
NFKB1 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta
POU2AF1 POU class 2 associating factor 1
PRKCD protein kinase C, delta
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
STK4 serine/threonine kinase 4
TNF tumor necrosis factor