|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
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1 gene mutations causing the absent subcommissural organ phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|RFX4||regulatory factor X, 4 (influences HLA class II expression)|