abnormal lymph node primary follicle morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of an unstimulated network of follicular dendritic cells and small resting B cells in the lymph node cortex (Mammalian Phenotype Ontology, MP_0002345)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002345
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Genes

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

Symbol Name
CHST4 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 4
FUT7 fucosyltransferase 7 (alpha (1,3) fucosyltransferase)
LTA lymphotoxin alpha
PBX1 pre-B-cell leukemia homeobox 1
SLC35C1 solute carrier family 35 (GDP-fucose transporter), member C1
TNF tumor necrosis factor
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B