翻訳と辞書 Words near each other ・ Multiple disabilities ・ Multiple discovery ・ Multiple discriminant analysis ・ Multiple dispatch ・ Multiple displacement amplification ・ Multiple document interface ・ Multiple drafts model ・ Multiple drug resistance ・ Multiple edges ・ Multiple EM for Motif Elicitation ・ Multiple encryption ・ Multiple endocrine neoplasia ・ Multiple endocrine neoplasia type 1 ・ Multiple endocrine neoplasia type 2 ・ Multiple endocrine neoplasia type 2b ・ Multiple Epidermal Growth Factor-like Domains 8 ・ Multiple epiphyseal dysplasia ・ Multiple Equivalent Simultaneous Offers ・ Multiple evanescent white dot syndrome ・ Multiple exciton generation ・ Multiple exposure ・ Multiple factor analysis ・ Multiple familial trichoepithelioma ・ Multiple follicular unit grafts ・ Multiple frames interface ・ Multiple frequency-shift keying ・ Multiple fruit ・ Multiple gamma function ・ Multiple granularity locking ・ Multiple gunshot suicide Dictionary Lists mini英和辞書 mini和英辞書 Webster 1913 Latin-English FOLDOC Wikipedia English ウィキペディア

翻訳と辞書　辞書検索 [ 開発暫定版 ] スポンサード リンク Multiple Epidermal Growth Factor-like Domains 8 ： ウィキペディア英語版 Multiple Epidermal Growth Factor-like Domains 8 ''Megf8'' also known as Multiple Epidermal Growth Factor-like Domains 8, is a protein coding gene that encodes a single pass membrane protein, known to participate in developmental regulation and cellular communication. It is located on chromosome 19 at the 49th open reading frame in humans (19q13.2). There are two isoform constructs known for MEGF8, which differ by a 67 amino acid indel. The isoform 2 splice version (analyzed throughout this page) is 2785 amino acids long, and predicted to be 296.6 kdal in mass. Isoform 1 is composed of 2845 amino acids and predicted to weigh 303.1 kdal. Using BLAST searches, orthologs were found primarily in mammals, but MEGF8 is also conserved in invertebrates and fishes, and rarely in birds, reptiles, and amphibians. A notably important paralog to multiple epidermal growth factor-like domains 8 is ATRNL1 (Attractin-like 1), which is also a single pass transmembrane protein, with several of the same key features and motifs as MEGF8, as indicated by Simple Modular Architecture Research Tool (SMART) which is hosted by the European Molecular Biology Laboratory located in Heidelberg, Germany. MEGF8 has been predicted to be a key player in several developmental processes, such as left-right patterning and limb formation.Currently, researchers have found MEGF8 SNP mutations to be the cause of Carpenter syndrome subtype 2. ==Gene== 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Multiple Epidermal Growth Factor-like Domains 8」の詳細全文を読む スポンサード リンク 翻訳と辞書 : 翻訳のためのインターネットリソース Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.