All transcripts active for the NR2E3 gene

This database is one of the "Eye disease" gene variant databases. It was established to group all sequence variant information on NR2E3-linked retinal degenerations, including enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), autosomal recessive retinitis pigmentosa (arRP) and autosomal dominant retinitis pigmentosa (adRP).
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ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00025608 15 transcript variant 2 NM_014249.3 NP_055064.1 424
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