Inositol polyphosphate 5-phosphatase OCRL: Difference between revisions
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==OCRL-1 mutations causing Lowe syndrome== | ==OCRL-1 mutations causing Lowe syndrome== | ||
== Oculocerebrorenal syndrome of Lowe == | == Oculocerebrorenal syndrome of Lowe == | ||
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OCRL1 has been also reported to localize to the basal body and the transition zone of the primary cilium. Therefore, it also participates in ciliogenesis by contributing to protein trafficking to this organelle in an Rab8/IPIP27-dependent manner.<ref name="cilia">PMID: 22228094</ref> | OCRL1 has been also reported to localize to the basal body and the transition zone of the primary cilium. Therefore, it also participates in ciliogenesis by contributing to protein trafficking to this organelle in an Rab8/IPIP27-dependent manner.<ref name="cilia">PMID: 22228094</ref> | ||
<StructureSection load='3qbt' size='340' side='right' caption='Caption for this structure' scene=''> | |||
== Mutations in OCRL1 == | == Mutations in OCRL1 == | ||
