RPGRIP1L 抗体
(RPGRIP1-Like (RPGRIP1L))
The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
Recommended next Filters:
21 results
Latest Publications for our RPGRIP1L 抗体
: "Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone." in: Scientific reports, Vol. 5, pp. 14096, (2015) (PubMed).: "CEP162 is an axoneme-recognition protein promoting ciliary transition zone assembly at the cilia base." in: Nature cell biology, Vol. 15, Issue 6, pp. 591-601, (2013) (PubMed).
: "Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome." in: Nature genetics, Vol. 39, Issue 7, pp. 882-8, (2007) (PubMed).
Aliases for RPGRIP1L 抗体
RPGRIP1 like (RPGRIP1L) 抗体RPGRIP1-like (rpgrip1l) 抗体
RPGRIP1 like (rpgrip1l) 抗体
Protein fantom (mks-5) 抗体
Rpgrip1-like (Rpgrip1l) 抗体
RPGRIP1 like (Rpgrip1l) 抗体
1700047E16Rik 抗体
4931437C01 抗体
cors3 抗体
CORS3 抗体
FTM 抗体
Ftm 抗体
jbts7 抗体
JBTS7 抗体
mks5 抗体
MKS5 抗体
nphp8 抗体
NPHP8 抗体
Nphp8 抗体
RGD1311099 抗体
si:ch1073-301i20.1 抗体
您还需要查找其他产品吗？
You are here:
