HAP1 knockout cell lines

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HAP1 Parental Cell Lines available

NT5C3A ( Human )

Entrez Gene 51251 entrezgene 51251
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5'-nucleotidase, cytosolic IIIA

Alias

NT5C3 | P5'N-1 | P5N-1 | PN-I | POMP | PSN1 | UMPH | UMPH1 | cN-III | hUMP1 | p36

This gene encodes a member of the 5'-nucleotidase family of enzymes that catalyze the dephosphorylation of nucleoside 5'-monophosphates. The encoded protein is the type 1 isozyme of pyrimidine 5' nucleotidase and catalyzes the dephosphorylation of pyrimidine 5' monophosphates. Mutations in this gene are a cause of hemolytic anemia due to uridine 5-prime monophosphate hydrolase deficiency. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and pseudogenes of this gene are located on the long arm of chromosomes 3 and 4. [provided by RefSeq, Mar 2012].