| Health / Medical Topics |
RAI1 wt Allele
Human RAI1 wild-type allele is located in the vicinity of 17p11.2 and is approximately 130 kb in length. This allele, which encodes retinoic acid-induced protein 1, plays roles in transcriptional regulation, development, control of body weight and complex behavioral responses. Mutations in this gene are associated with Smith-Magenis Syndrome. (NCI Thesaurus)
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This gene is involved in transcription, development and behavior.
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