亚洲一区二区在线-蜜桃视频网-欧美日韩精品一区二区三区-91性视频-午夜不卡视频-日韩无码精品一区二区-国产艳妇疯狂做爰视频-沈清秋屁股扒开臀缝调教-毛片精品-亚洲视频图片-国产视频网站在线观看-清清草免费视频-午夜影院视频-日日艹夜夜艹-青青导航-人人人超碰-日韩一区高清-国产精品羞羞答答在线-午夜网站在线-老外的吊大我受不了-国产 日韩 一区-自拍偷拍欧美日韩-国产片大尺度裸露床戏-欧美激情一区二区三区免费观看-a天堂亚洲-蜜桃av麻豆-爱的色放 韩国-成年人一级电影-免费色黄视频-综合在线亚洲

This gene encodes the catalytic subunit of protein phosphatase, a component of a signaling pathway regulating cell cycle progression. Splice variants encoding different protein isoforms exist. The pseudogene of this gene is located on chromosome X. [provided by RefSeq, Jul 2008]

The NDRG3 protein is a 41 kDa cytoplasmic protein that exists in three isoforms, the first of which is the canonical 41 kDa, 375 amino acid form. It is a member of the NDRG family of proteins and is involved in cell differentiation and negative regulation of cell growth.

The melanocortin family comprises the Alpha-, Beta- and Gamma- melanocyte stimulating hormones (MSH) and adrenocorticotrophin. The receptors for these hormones are seven-transmembrane G protein-coupled proteins that activate adenylyl cyclase. Five melanocortin receptors have been cloned and shown to exhibit different affinities and patterns of expression. MC1-R (MSH-R) is expressed in melanocytes and corticoadrenal tissue. MC2-R is the ACTH receptor and is expressed primarily in the adren

NCR2 (NKp44) is a member of the natural cytotoxicity receptor (NCR) family that is expressed on activated human NK cells. NCR2 displays a single extracellular Ig-like V domain and a transmembrane portion containing the charged residue (Lysine), likely involved in the association with KARAP/DAP12 molecules. Gene coding for NCR2 maps on human chromosome 6p21.1

This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration. [provided by RefSeq, Jul