absent subcommissural organ Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the circumventricular organ derived from ependymal cells that is located at the junction of the third ventricle and the cerebral aqueduct and which secretes somatostatin (Mammalian Phenotype Ontology, MP_0009717)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009717
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1 gene mutations causing the absent subcommissural organ phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
RFX4 regulatory factor X, 4 (influences HLA class II expression)