人 TMEM67 (NM_153704) cDNA克隆

Accession: NM_153704
基因名称: TMEM67
基因别名: MKS3; JBTS6; NPHP11; TNEM67; MECKELIN
基因描述: Homo sapiens transmembrane protein 67 (TMEM67), transcript variant 1, mRNA.
种属: Human
CDS区长度: 2988 (查看编码区序列)
翻译后氨基酸长度: 995 (查看氨基酸序列)
Transcript Variant: This variant (1) represents the longest transcript and encodes the longer protein (isoform 1).
产品编号 产品名称 载体 规格 价格
G104642 人 TMEM67 (NM_153704) cDNA克隆 pDONR223 2ug质粒 点击询价

The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008]