abnormal inguinal lymph node morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the lymph nodes located in the groin area (Mammalian Phenotype Ontology, MP_0002353)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002353
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Genes

20 gene mutations causing the abnormal inguinal lymph node morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CXCL13 chemokine (C-X-C motif) ligand 13
CXCR5 chemokine (C-X-C motif) receptor 5
GPR132 G protein-coupled receptor 132
HR hair growth associated
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL7 interleukin 7
IRF2 interferon regulatory factor 2
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)
NOS2 nitric oxide synthase 2, inducible
PLCD1 phospholipase C, delta 1
PRKCH protein kinase C, eta
RAG1 recombination activating gene 1
RUNX1 runt-related transcription factor 1
TNF tumor necrosis factor
TOX thymocyte selection-associated high mobility group box