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Alanine Glyoxylate Aminotransferase Proteine (AGXT)

Alanine Glyoxylate Aminotransferase Proteine (AGXT)
Auf finden Sie aktuell 11 Alanine Glyoxylate Aminotransferase (AGXT) Proteine von 5 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen Alanine Glyoxylate Aminotransferase Antikörper (84) und Alanine Glyoxylate Aminotransferase Kits (5) und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 108 Alanine Glyoxylate Aminotransferase Produkte verfügbar.
AGT, Agt1, Agxt1, PH1, Spat, SPT, TLH6
alle Proteine anzeigen Gen GeneID UniProt
AGXT 189 P21549
AGXT 11611 O35423
AGXT 24792 P09139

Weitere Synonyme anzeigen

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Weitere Proteine zu Alanine Glyoxylate Aminotransferase Interaktionspartnern

Human Alanine Glyoxylate Aminotransferase (AGXT) Interaktionspartner

  1. Novel AGXT mutations in a Tunisian population with primary hyperoxaluria type 1.

  2. The novel p.Gln137Hisfs*19 AGXT mutation detected in this study extends the spectrum of known primary hyperoxaluria type I AGXT gene mutations in Tunisia.

  3. Data show that onomeric minor allele of human alanine glyoxylate aminotransferase (AGT-Mi) binds pyridoxal 5-phosphate (PLP (zeige PLP1 Proteine)) but does not display catalytic activity.

  4. Letter/Case Report: novel missense AGXT gene mutation in a Sri (zeige SRI Proteine) Lankan family with primary hyperoxaluria type 1.

  5. Primary hyperoxaluria type 1 (PH1) is due to a defect in the AGXT gene. The aim of our study was to analyze the mutations causing PH1 in the Moroccan population

  6. The pathogenic mutation G47R causes misfolding of alanine:glyoxylate aminotransferase (zeige AGT Proteine).

  7. A review of the current knowledge of the biochemical properties of liver peroxisomal alanine:glyoxylate aminotransferase (zeige AGT Proteine) and of the molecular defects caused by single point mutations associated with Primary Hyperoxaluria Type 1.

  8. S81L and G170R mutations of AGT is associated with Primary Hyperoxaluria type I in homozygosis and heterozygosis.

  9. AGT missense mutations associated with Primary Hyperoxaluria Type 1, were characterized.

  10. Data suggest that dequalinium chloride (DECA) may be a pharmacologic strategy to treat primary hyperoxaluria 1 (PH1) patients with mutations in alanine:glyoxylate aminotransferase (AGT (zeige AGT Proteine)).

Mouse (Murine) Alanine Glyoxylate Aminotransferase (AGXT) Interaktionspartner

  1. expressed wild-type human AGT1 was predominantly localized in mouse hepatocellular peroxisomes, whereas the most common mutant form of AGT1 (G170R) was localized predominantly in the mitochondria

Alanine Glyoxylate Aminotransferase (AGXT) Protein Überblick

Protein Überblick

This gene is expressed only in the liver and the encoded protein is localized mostly in the peroxisomes, where it is involved in glyoxylate detoxification. Mutations in this gene, some of which alter subcellular targetting, have been associated with type I primary hyperoxaluria.

Alternative names and synonyms associated with Alanine Glyoxylate Aminotransferase (AGXT)

  • alanine-glyoxylate aminotransferase (AGXT)
  • alanine-glyoxylate aminotransferase (Agxt)
  • AGT Protein
  • Agt1 Protein
  • Agxt1 Protein
  • PH1 Protein
  • Spat Protein
  • SPT Protein
  • TLH6 Protein

Bezeichner auf Proteinebene für AGXT

L-alanine: glyoxylate aminotransferase 1 , alanine--glyoxylate aminotransferase , hepatic peroxisomal alanine:glyoxylate aminotransferase , serine--pyruvate aminotransferase , serine-pyruvate aminotransferase , serine:pyruvate aminotransferase , alanine-glyoxylate aminotransferase 1 , serine--pyruvate aminotransferase, mitochondrial , serine--pyruvate aminotransferase, peroxisomal , angiotensin receptor 2 , serine:pyruvate aminotransferase SPT , serine:pyruvate/alanine:glyoxylate aminotransferase , AGT , SPT , alanine:glyoxylate aminotransferase

189 Homo sapiens
11611 Mus musculus
24792 Rattus norvegicus
727692 Felis catus
100009147 Oryctolagus cuniculus
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