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AGXT2, alanine--glyoxylate aminotransferase 2

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AGXT2, alanine--glyoxylate aminotransferase 2

  • The protein encoded by this gene is a class III pyridoxal-phosphate-dependent mitochondrial aminotransferase. It catalyzes the conversion of glyoxylate to glycine using L-alanine as the amino donor. It is an important regulator of methylarginines and is involved in the control of blood pressure in kidney. Polymorphisms in this gene affect methylarginine and beta-aminoisobutyrate metabolism, and are associated with carotid atherosclerosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]

  • Gene Synonyms (alanine--glyoxylate aminotransferase 2, mitochondrial, (R)-3-amino-2-methylpropionate--pyruvate transaminase, beta-ALAAT II, beta-alanine-pyruvate aminotransferase, AGT2, BAIBA, DAIBAT,)
  • NCBI Gene ID: 64902
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9BYV1
  • 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.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

alanine--glyoxylate aminotransferase 2 interacts with:

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.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

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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