Literature summary for 1.5.1.20 extracted from

Rallidis, L.S.; Gialeraki, A.; Komporozos, C.; Vavoulis, P.; Pavlakis, G.; Travlou, A.; Lekakis, I.; Kremastinos, D.T.
Role of methylenetetrahydrofolate reductase 677C->T polymorphism in the development of premature myocardial infarction (2008), Atherosclerosis, 200, 115-120.

Search for more literature for 1.5.1.20

Protein Variants

Protein Variants	Comment	Organism
additional information	homozygocity for the C677T gene mutation of MTHFR is independently associated with the development of premature with premature myocardial infarction and normal coronary arteries	Homo sapiens
additional information	increased MTHFR 677T allele load confers risk for negative symptoms in schizophrenia, while reducing severity of positive symptoms, the biochemical interaction of low serum folate with 677T-variant MTHFR may induce downstream effects salient to the expression of negative symptoms	Homo sapiens

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	-	-	-

Source Tissue

Source Tissue	Comment	Organism	Textmining
blood	-	Homo sapiens	-
serum	-	Homo sapiens	-

Synonyms

Synonyms	Comment	Organism
5,10-methylenetetrahydrofolate reductase	-	Homo sapiens
methylenetetrahydrofolate reductase	-	Homo sapiens
MTHFR	-	Homo sapiens

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Release 2023.1 (January 2023)