decreased total retina thickness Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decreased width of the retina through the center plane (Mammalian Phenotype Ontology, MP_0011965)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011965
Similar Terms
Downloads & Tools

Genes

9 gene mutations causing the decreased total retina thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATOH7 atonal homolog 7 (Drosophila)
CCND1 cyclin D1
LAMB2 laminin, beta 2 (laminin S)
MARCKSL1 MARCKS-like 1
MERTK MER proto-oncogene, tyrosine kinase
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
PRPH2 peripherin 2 (retinal degeneration, slow)
UNC119 unc-119 homolog (C. elegans)
VSX2 visual system homeobox 2