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This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
, Golgi 3-prime phosphoadenosine 5-prime phosphate 3-prime phosphatase
, IMPase 3
, golgi-resident PAP phosphatase
, inositol monophosphatase 3
, inositol monophosphatase domain-containing protein 1
, inositol-1(or 4)-monophosphatase 3
, myo-inositol monophosphatase A3
, IMP 3
, inositol monophosphatase domain containing 1
, inositol monophosphatase 3-like
, Golgi-resident PAP phosphatase
, Inositol monophosphatase domain-containing protein 1
, Inositol-1(or 4)-monophosphatase 3
, Myo-inositol monophosphatase A3
, LOW QUALITY PROTEIN: inositol monophosphatase 3