abnormal lymph organ development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process of morphological maturation of the organs of the lymph system (Mammalian Phenotype Ontology, MP_0002450)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002450
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10 gene mutations causing the abnormal lymph organ development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
CALCRL calcitonin receptor-like
CBFB core-binding factor, beta subunit
EGLN1 egl-9 family hypoxia-inducible factor 1
LTA lymphotoxin alpha
NPRL3 nitrogen permease regulator-like 3 (S. cerevisiae)
PROX1 prospero homeobox 1
RAMP2 receptor (G protein-coupled) activity modifying protein 2
RORC RAR-related orphan receptor C
RUNX1 runt-related transcription factor 1