abnormal primary vitreous morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the fibrovascular mesodermal tissue located between the optic cup and lens vesicle that normally regresses during the development of the vitreous body (Mammalian Phenotype Ontology, MP_0009620)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009620
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Genes

8 gene mutations causing the abnormal primary vitreous morphology 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
CEP41 centrosomal protein 41kDa
NOTCH2 notch 2
RARB retinoic acid receptor, beta
RXRA retinoid X receptor, alpha
STRA6 stimulated by retinoic acid 6
TGFB2 transforming growth factor, beta 2