Literature summary for 2.1.1.5 extracted from

Ananth, C.V.; Elsasser, D.A.; Kinzler, W.L.; Peltier, M.R.; Getahun, D.; Leclerc, D.; Rozen, R.R.; Rozen, R.R.
Polymorphisms in methionine synthase reductase and betaine-homocysteine S-methyltransferase genes: risk of placental abruption (2007), Mol. Genet. Metab., 91, 104-110.

Search for more literature for 2.1.1.5

Application

Application	Comment	Organism
medicine	a polymorphisms in betaine-homocysteine S-methyltransferase might be linked to an increased risk for placental abruption	Homo sapiens

Protein Variants

Protein Variants	Comment	Organism
G742A	in an ongoing, multicenter, case-control study including women with a clinical diagnosis of abruption an association between the homozygous mutant form of BHMT (742G to A) polymorphism and an increased risk for placental abruption is shown	Homo sapiens

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	-	-	-

Synonyms

Synonyms	Comment	Organism
betaine-homocysteine S-methyltransferase	-	Homo sapiens
BHMT	-	Homo sapiens

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Release 2023.1 (January 2023)