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Phenotypic Alleles
Query Results -- Summary
 Symbol
Name
ID
Nr2e3
nuclear receptor subfamily 2, group E, member 3
MGI:1346317

2 matching Alleles (1 Gene/Marker represented)
                                    Allele Symbol
Name Chr Synonyms Category Phenotypic Classes Human Diseases Nr2e3rd7
nuclear receptor subfamily 2, group E, member 3; retinal degeneration 7
images 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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory