abnormal mammillary body morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the protrusion at the posterior end of the hypothalamus that contains hypothalamic nuclei (Mammalian Phenotype Ontology, MP_0004162)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004162
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Genes

1 gene mutations causing the abnormal mammillary body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXB1 forkhead box B1