TMEM67 抗体
(Transmembrane Protein 67 (TMEM67))
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].
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Latest Publications for our TMEM67 抗体
: "Meckelin 3 is necessary for photoreceptor outer segment development in rat Meckel syndrome." in: PLoS ONE, Vol. 8, Issue 3, pp. e59306, (2013) (PubMed).Aliases for TMEM67 抗体
transmembrane protein 67 (TMEM67) 抗体transmembrane protein 67 (tmem67) 抗体
transmembrane protein 67 (Tmem67) 抗体
5330408M12Rik 抗体
b2b1163.1Clo 抗体
b2b1291.1Clo 抗体
B230117O07 抗体
JBTS6 抗体
MECKELIN 抗体
MKS3 抗体
NPHP11 抗体
TNEM67 抗体
Wpk 抗体
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