absent spleen marginal zone Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the zone between the red and white pulp of the spleen containing numerous macrophages and lymphocytes, and a rich plexus of sinusoids supplied by white pulp arterioles carrying blood-borne antigens (Mammalian Phenotype Ontology, MP_0008234)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008234
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10 gene mutations causing the absent spleen marginal zone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
B3GNT5 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5
FOXP3 forkhead box P3
LTA lymphotoxin alpha
LTB lymphotoxin beta (TNF superfamily, member 3)
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
SFN stratifin
SHARPIN SHANK-associated RH domain interactor
TNF tumor necrosis factor