OCRL

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oculocerebrorenal syndrome of Lowe
Identifiers
Symbol	OCRL
Entrez	4952
HUGO	8108
OMIM	300535
RefSeq	NM_000276
UniProt	Q01968
Other data
EC number	3.1.3.36
Locus	Chr. X q25-q26.1

OCRL is a gene on the X chromosome associated with oculocerebrorenal syndrome.

[edit] External links

• MeSH OCRL+protein,+human

v • d • e Hydrolase: esterases (EC 3.1) 3.1.1: Carboxylic ester hydrolases Cholinesterase - Pectinesterase - 6-phosphogluconolactonase - PAF acetylhydrolase Lipase (Gastric/Lingual, Pancreatic, Lysosomal, Hormone-sensitive, Endothelial, Hepatic, Lipoprotein, Monoacylglycerol, Diacylglycerol) Phospholipase (A1, A2, B) 3.1.2: Thioesterase Palmitoyl thioesterase - Ubiquitin carboxy-terminal hydrolase L1 3.1.3: Phosphatase Alkaline phosphatase - Acid phosphatase (Prostatic)/Tartrate resistant acid phosphatase/Purple acid phosphatases - Nucleotidase - Glucose 6-phosphatase - Fructose 1,6-bisphosphatase - Calcineurin - Phosphoprotein phosphatase (PP2A) - OCRL - Pyruvate dehydrogenase phosphatase - Fructose 2,6-bisphosphatase - Protein tyrosine phosphatase - PTEN 3.1.4: Phosphodiesterase Autotaxin - Phospholipase (C, D) - Sphingomyelin phosphodiesterase - PDE1 - PDE2 - PDE3 - PDE5 3.1.6: Sulfatase Arylsulfatase B - Steroid sulfatase - Galactosamine-6 sulfatase - Arylsulfatase A - Iduronate-2-sulfatase - N-acetylglucosamine-6-sulfatase other Nuclease