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IMPAD1

Official Full Name
3'(2'), 5'-bisphosphate nucleotidase 2
Organism
Homo sapiens
GeneID
54928
Background
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. [provided by RefSeq, Dec 2011]
Synonyms
BPNT2; GPAPP; IMP 3; IMP-3; IMPA3; IMPAD1;

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