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Literature summary for 4.1.1.90 extracted from

  • Qiao, J.; Wang, T.; Yang, J.; Liu, J.; Gong, X.; Guo, X.; Wang, S.; Ye, Z.
    Genetic mutation of vitamin K-dependent gamma-glutamyl carboxylase domain in patients with calcium oxalate urolithiasis (2009), J. Huazhong Univ. Sci. Technol. Med. Sci., 29, 604-608.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Homo sapiens
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-
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Source Tissue

Source Tissue Comment Organism Textmining

Synonyms

Synonyms Comment Organism
GGCX
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Homo sapiens
vitamin K-dependent gamma-glutamyl carboxylase
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Homo sapiens

General Information

General Information Comment Organism
physiological function functional GGCX mutations in all 15 exons do not occur in most calcium oxalate urolithiasis patients, thus no significant association between the low activity and mutation of GGCX in calcium oxalate urolithiasis Homo sapiens