OCRL
oculocerebrorenal syndrome of Lowe
Sinónimos:
INPP5F, LOCR, NPHL2, OCRL-1, OCRL1
Especie:
Human OCRL (4952), Mouse Ocrl (320634), Rat Ocrl (317576), Zebrafish ocrl (777716), fruit fly Ocrl (31157), Horse OCRL (100059144), dog OCRL (492123), domestic cat OCRL (101101038), chicken OCRL (422136), naked mole-rat Ocrl (101722262) ...Más
ID UniProtKB:
ID del gen:
- Human(4952) Summary: 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]
- Mouse(320634) oculocerebrorenal syndrome of Lowe
- Rat(317576) oculocerebrorenal syndrome of Lowe
- Zebrafish(777716) oculocerebrorenal syndrome of Lowe
- fruit fly(31157) Oculocerebrorenal syndrome of Lowe 1 ortholog
- Horse(100059144) oculocerebrorenal syndrome of Lowe
- dog(492123) oculocerebrorenal syndrome of Lowe
- domestic cat(101101038) oculocerebrorenal syndrome of Lowe
- chicken(422136) oculocerebrorenal syndrome of Lowe
- naked mole-rat(101722262) oculocerebrorenal syndrome of Lowe
- domestic guinea pig(100733180) oculocerebrorenal syndrome of Lowe
- Domestic Rabbit(100346052) oculocerebrorenal syndrome of Lowe
- sheep(101119794) oculocerebrorenal syndrome of Lowe
- cow(535844) oculocerebrorenal syndrome of Lowe
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