opacity of vitreous body Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the transparent gel filling the inner portion of the eyeball between the lens and retina becomes cloudy and impervious to light (Mammalian Phenotype Ontology, MP_0002700)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002700
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6 gene mutations causing the opacity of vitreous body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASXL1 additional sex combs like transcriptional regulator 1
BMP4 bone morphogenetic protein 4
CDKN2A cyclin-dependent kinase inhibitor 2A
CSRP2BP CSRP2 binding protein
GSK3A glycogen synthase kinase 3 alpha
TP53 tumor protein p53