The following gene names and symbols are associated with antigen Oculocerebrorenal Syndrome of Lowe across different species:

oculocerebrorenal syndrome of Lowe (OCRL), phosphatidylinositol polyphosphate 5-phosphatase (NAEGRDRAFT_58601), oculocerebrorenal syndrome of Lowe (Ocrl), oculocerebrorenal syndrome of Lowe (ocrl)

Other aliases include:

LOCR, NPHL2, OCRL1, INPP5F, BB143339, 9530014D17Rik, OCRL, MGC179390, wu:fi09g03, zgc:152864, locr, nphl2, ocrl1, inpp5f, DKFZp469O216

On the protein level the following designations are being used for antigen Oculocerebrorenal Syndrome of Lowe:

phosphatidylinositol polyphosphate 5-phosphatase – Lowe oculocerebrorenal syndrome protein – oculocerebrorenal syndrome of Lowe – inositol polyphosphate 5-phosphatase OCRL-1 – OTTMUSP00000019179 – OTTMUSP00000019180 – phosphatidylinositol polyphosphate 5-phosphotase – phosphatidylinositol polyphosphate 5-phosphatase-like – inositol polyphosphate 5-phosphatase OCRL-1-like

Oculocerebrorenal Syndrome of Lowe fulfills a number of functions:

hydrolase activity – inositol or phosphatidylinositol phosphatase activity – phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity – molecular_function

Oculocerebrorenal Syndrome of Lowe is relevant to the following processes:

lipid metabolic process – signal transduction – biological_process – phosphoinositide dephosphorylation

Locations for Oculocerebrorenal Syndrome of Lowe:

Golgi stack – Golgi-associated vesicle – intracellular – cellular_component – Golgi apparatus

Source: NCBI Entrez Gene, Gene Ontology