intermingled spleen red and white pulp Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description no clear demarcation of the spleen red and white pulp tissue (Mammalian Phenotype Ontology, MP_0008475)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008475
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Genes

13 gene mutations causing the intermingled spleen red and white pulp phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALOX15 arachidonate 15-lipoxygenase
B3GNT5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5
BCL3 B-cell CLL/lymphoma 3
FLT3 fms-related tyrosine kinase 3
FOXP3 forkhead box P3
IKZF1 IKAROS family zinc finger 1 (Ikaros)
LAMP2 lysosomal-associated membrane protein 2
LTB lymphotoxin beta (TNF superfamily, member 3)
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
NKX2-3 NK2 homeobox 3
PCSK1 proprotein convertase subtilisin/kexin type 1
SELL selectin L
TNF tumor necrosis factor