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NR2E3 gene

nuclear receptor subfamily 2 group E member 3

Key facts

Official symbol
NR2E3
Full name
NR2E3
Chromosome
15
Map location
15q23
Organism
Homo sapiens
NCBI Gene ID
10002
Also known as
ESCS, ESCS1, PNR, RNR, RP37, rd7

Function summary

This protein is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in adults. Members of this family are characterized by discrete domains that function in DNA and ligand binding. This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008].

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Data source: NCBI Gene · alsesAI Gene Library