Lentiviral human HR sgRNA gene knockout kit

Human HR

Gene symbol: HR
Synonyms: ALUNC AU HSA277165 HYPT4 MUHH MUHH1
Species: HUMAN
Gene ID: 55806
Summary: This gene encodes a protein that is involved in hair growth. This protein functions as a transcriptional corepressor of multiple nuclear receptors, including thyroid hormone receptor, the retinoic acid receptor-related orphan receptors and the vitamin D receptors, and it interacts with histone deacetylases. The translation of this protein is modulated by a regulatory open reading frame (ORF) that exists upstream of the primary ORF. Mutations in this upstream ORF cause Marie Unna hereditary hypotrichosis (MUHH), an autosomal dominant form of genetic hair loss. Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions, other diseases resulting in hair loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2014].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_005144:3:2 NM_018411:3:2