vitreous body deposition Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal accumulation of material in the vitreous body (Mammalian Phenotype Ontology, MP_0006200)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006200
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Genes

7 gene mutations causing the vitreous body deposition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASXL1 additional sex combs like transcriptional regulator 1
LARGE like-glycosyltransferase
MSX2 msh homeobox 2
NDP Norrie disease (pseudoglioma)
PXDN peroxidasin
RARB retinoic acid receptor, beta
TGFB2 transforming growth factor, beta 2