retina hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, in the thin layer of neural tissue lining the back of the eyeball which contains visual receptors (Mammalian Phenotype Ontology, MP_0002984)
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7 gene mutations causing the retina hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
C1QTNF5 C1q and tumor necrosis factor related protein 5
CCND1 cyclin D1
FOXN4 forkhead box N4
POU4F2 POU class 4 homeobox 2
RPL24 ribosomal protein L24
SIX6 SIX homeobox 6
TBC1D32 TBC1 domain family, member 32