abnormal axillary 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 around the axillary vein that receive lymphatic drainage from the upper or forelimb, scapular region and pectoral region (Mammalian Phenotype Ontology, MP_0002340)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002340
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Genes

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

Symbol Name
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CXCL13 chemokine (C-X-C motif) ligand 13
CXCR5 chemokine (C-X-C motif) receptor 5
IKZF1 IKAROS family zinc finger 1 (Ikaros)
IL7 interleukin 7
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)
PLCD1 phospholipase C, delta 1
PRKCH protein kinase C, eta
RUNX1 runt-related transcription factor 1
TNF tumor necrosis factor
TOP3B topoisomerase (DNA) III beta
TOX thymocyte selection-associated high mobility group box