abnormal nucleotide metabolism Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the chemical reactions and pathways involving a nucleotide, including metabolic, catabolic and biosynthetic processes (Mammalian Phenotype Ontology, MP_0003806)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003806
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Genes

12 gene mutations causing the abnormal nucleotide metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADA adenosine deaminase
ADK adenosine kinase
AK1 adenylate kinase 1
AMPD3 adenosine monophosphate deaminase 3
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
NQO1 NAD(P)H dehydrogenase, quinone 1
OTC ornithine carbamoyltransferase
TALDO1 transaldolase 1
TPMT thiopurine S-methyltransferase
TYMP thymidine phosphorylase
UPP1 uridine phosphorylase 1
VPS54 vacuolar protein sorting 54 homolog (S. cerevisiae)