abnormal brachial 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 along the brachial vein that receive drainage from most of the free upper limb and send efferent vessels to the central axillary lymph nodes (Mammalian Phenotype Ontology, MP_0005231)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005231
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Genes

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

Symbol Name
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CXCL13 chemokine (C-X-C motif) ligand 13
CXCR5 chemokine (C-X-C motif) receptor 5
LTA lymphotoxin alpha
LTB lymphotoxin beta (TNF superfamily, member 3)
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
PRKCH protein kinase C, eta
TNF tumor necrosis factor