absent inguinal lymph nodes Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the lymph nodes normally located in the groin area (Mammalian Phenotype Ontology, MP_0009622)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009622
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Genes

10 gene mutations causing the absent inguinal lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CXCL13 chemokine (C-X-C motif) ligand 13
CXCR5 chemokine (C-X-C motif) receptor 5
IKZF1 IKAROS family zinc finger 1 (Ikaros)
LTA lymphotoxin alpha
LTB lymphotoxin beta (TNF superfamily, member 3)
MAP3K14 mitogen-activated protein kinase kinase kinase 14
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)
TNF tumor necrosis factor
TOX thymocyte selection-associated high mobility group box