Symbol Name ID

Nr2e3 nuclear receptor subfamily 2, group E, member 3 MGI:1346317

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2 matching Alleles (1 Gene/Marker represented)

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                                    Allele Symbol
Name                                       Chr  Synonyms        Category                 Phenotypic Classes                       Human Diseases           

Nr2e3rd7
nuclear receptor subfamily 2, group E, member 3; retinal degeneration 7
             9    rd7       Spontaneous           cellular, nervous system, vision/eye  Enhanced S-Cone Syndrome; ESCS 268100

Nr2e3tm1Dgen
nuclear receptor subfamily 2, group E, member 3; targeted mutation 1, Deltagen  9              Targeted (knock-out)  vision/eye