OCRL 抗体
(Oculocerebrorenal Syndrome of Lowe (OCRL))
This gene encodes a phosphatase enzyme that is involved in actin polymerization and is found in the trans-Golgi network. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. [provided by RefSeq, Jul 2008].
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Latest Publications for our OCRL 抗体
: "Recruitment of OCRL and Inpp5B to phagosomes by Rab5 and APPL1 depletes phosphoinositides and attenuates Akt signaling." in: Molecular biology of the cell, Vol. 23, Issue 1, pp. 176-87, (2012) (PubMed).Aliases for OCRL 抗体
OCRL, inositol polyphosphate-5-phosphatase (Ocrl) 抗体phosphatidylinositol polyphosphate 5-phosphatase (NAEGRDRAFT_58601) 抗体
OCRL, inositol polyphosphate-5-phosphatase (OCRL) 抗体
oculocerebrorenal syndrome of Lowe (ocrl) 抗体
OCRL, inositol polyphosphate-5-phosphatase (ocrl) 抗体
9530014D17Rik 抗体
BB143339 抗体
inpp5f 抗体
INPP5F 抗体
locr 抗体
LOCR 抗体
nphl2 抗体
NPHL2 抗体
OCRL 抗体
OCRL-1 抗体
ocrl1 抗体
OCRL1 抗体
wu:fi09g03 抗体
zgc:152864 抗体
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