SMCR2
In molecular biology, Smith-Magenis syndrome chromosome region, candidate 2 (non-protein coding), also known as SMCR2 is a long non-coding RNA. In humans, it is found in a region of chromosome 17 that is commonly deleted in Smith–Magenis syndrome.[1]
See also
[edit]References
[edit]- ^ Bi W, Yan J, Stankiewicz P, Park SS, Walz K, Boerkoel CF, et al. (2002). "Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse". Genome Res. 12 (5): 713–728. doi:10.1101/gr.73702. PMC 186594. PMID 11997338.
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