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NR4A2

Official Full Name
nuclear receptor subfamily 4 group A member 2
Organism
Homo sapiens
GeneID
4929
Background
This gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily. The encoded protein may act as a transcription factor. Mutations in this gene have been associated with disorders related to dopaminergic dysfunction, including Parkinson disease, schizophernia, and manic depression. Misregulation of this gene may be associated with rheumatoid arthritis. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Synonyms
NOT; RNR1; HZF-3; IDLDP; NURR1; TINUR;

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