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NT5C3A, 5'-nucleotidase, cytosolic IIIA

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NT5C3A, 5'-nucleotidase, cytosolic IIIA

  • 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]

  • Gene Synonyms (cytosolic 5'-nucleotidase 3A, 5'-nucleotidase, cytosolic III, 7-methylguanosine phosphate-specific 5'-nucleotidase, cytosolic 5'-nucleotidase 3, lupin, pyrimidine 5'-nucleotidase 1, uridine 5'-monophosphate hydrolase 1, NT5C3, P5'N-1, P5N-1, PN-I, POMP, PSN1, UMPH, UMPH1, cN-III, hUMP1, p36,)
  • NCBI Gene ID: 51251
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A024RA81
    UNIPROT ID#>>Q9H0P0
    UNIPROT ID#>>A0A090N7U2
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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