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Gene entry

AGXT

alanine--glyoxylate aminotransferase

Chromosome
2
Cytoband
2q37.3
Variants (rsID)
49

AGXT is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q37.3). Its official name is “alanine--glyoxylate aminotransferase”. The reference table lists 49 variants (rsID) for this gene.

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Clinically classified variants

46 reference-table entries with clinical significance.

  • rs115014558Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs115057148Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs11693280Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs117195882Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs140992177Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177176Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs33958047Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs34116584Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs34885252Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs35698882Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs35977912Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs4273214Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs4344931Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs4426527Benignsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs147601535Conflicting interpretationssingle nucleotide variantPrimary hyperoxaluria, type I|Primary hyperoxaluria
  • rs61729604Conflicting interpretationssingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177238Likely pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177259Likely pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177294Likely pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177193OtherDuplicationHyperoxaluria, Primary, Type I
  • rs180177196Othersingle nucleotide variant
  • rs180177275OtherInsertionHyperoxaluria, Primary, Type I
  • rs121908520Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs121908521Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs121908522Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs121908523Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I|Nephrocalcinosis|Nephrolithiasis
  • rs121908524Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I|Primary hyperoxaluria
  • rs121908525Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I|Primary hyperoxaluria|Nephrocalcinosis|Nephrolithiasis
  • rs121908526Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs121908528Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs121908529Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I|Primary hyperoxaluria
  • rs121908530Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I|Primary hyperoxaluria
  • rs180177156Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I|Primary hyperoxaluria
  • rs180177157Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177168Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177195Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177197Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177207Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I|Abnormality of metabolism/homeostasis
  • rs180177225Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177239Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177253Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177267Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I|Primary hyperoxaluria
  • rs180177286Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs180177298Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs796052064Pathogenicsingle nucleotide variantPrimary hyperoxaluria, type I
  • rs376844297Uncertain significancesingle nucleotide variantPrimary hyperoxaluria, type I

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.