absent retinal rod cells Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of one of the photoreceptor cell types of the vertebrate retina, in which the photopigment is in stacks of membranous disks separate from the outer cell membrane (Mammalian Phenotype Ontology, MP_0008454)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008454
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Genes

5 gene mutations causing the absent retinal rod cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MITF microphthalmia-associated transcription factor
NRL neural retina leucine zipper
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
PRPH2 peripherin 2 (retinal degeneration, slow)
RD3 retinal degeneration 3