|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||absence of the photoreceptor region which contains the machinery of the cell (mitochondria, golgi, endoplasmic reticulum, etc) and where opsin molecules are assembled and passed to be part of the outer segment region (Mammalian Phenotype Ontology, MP_0008583)|
|Downloads & Tools|
4 gene mutations causing the absent photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.