persistent hyperplastic primary vitreous Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description NT MGI. (Human Disease Ontology, DOID_0060282)
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6 gene mutations causing the persistent hyperplastic primary vitreous phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALDH1A3 aldehyde dehydrogenase 1 family, member A3
CDKN2A cyclin-dependent kinase inhibitor 2A
NOTCH2 notch 2
RARB retinoic acid receptor, beta
RXRA retinoid X receptor, alpha
STRA6 stimulated by retinoic acid 6