成年男人裸j网站 I 精品日产卡一卡二卡三入口 I 欧美黑人粗大xxxxx猛交 I 国产视频在线免费观看 I 日本特黄成人 I 免费无码av污污污在线观看 I 美国一区二区三区无码视频 I 亚洲欧美日韩一区二区三区四区 I 国产jjizz女人多水 I 日韩久久影视 I 91亚洲国产成人精品一区二三 I 老司机久久精品 I 屁屁国产第一页草草影院 I 我我色综合 I 成人免费大片黄在线播放 I 欧美三级在线电影免费 I 国产伊人网 I 精品久久久久99 I 末发育娇小性色xxxxx I 荔枝污 I 国产寡妇亲子伦一区二区三区四区 I 国产三级黄色片 I 秋霞久久久久久一区二区 I 95精品视频 I 超碰碰碰 I 特级黄色一级大片 I 视频在线日韩 I 亚洲成年人网

This gene encodes a member of the homer family of dendritic proteins. Members of this family regulate group 1 metabotrophic glutamate receptor function. [provided by RefSeq, Jul 2008]

This gene encodes a serine/threonine protein kinase related to the dual specific mitogen-activated protein kinase kinase (MAPKK) family. Evidence suggests that mitotic phosphorylation is required for its catalytic activity. The encoded protein may be involved in the activation of lymphoid cells and support testicular functions, with a suggested role in the process of spermatogenesis. Overexpression of this gene has been implicated in tumorigenesis. Alternative splicing results in multiple tran

May mediate anti-apoptotic activity.

Related to nucleologenesis, may play a role in the maintenance of the fundamental structure of the fibrillar center and dense fibrillar component in the nucleolus. It has intrinsic GTPase and ATPase activities. May play an important role in transcription catalyzed by RNA polymerase I.

This gene belongs to the TMEM43 family. Defects in this gene are the cause of familial arrhythmogenic right ventricular dysplasia type 5 (ARVD5), also known as arrhythmogenic right ventricular cardiomyopathy type 5 (ARVC5). Arrhythmogenic right ventricular dysplasia is an inherited disorder, often involving both ventricles, and is characterized by ventricular tachycardia, heart failure, sudden cardiac death, and fibrofatty replacement of cardiomyocytes. This gene contains a response element f