Literature summary for 1.16.1.8 extracted from

Cheng, H.; Li, H.; Bu, Z.; Zhang, Q.; Bai, B.; Zhao, H.; Li, R.K.; Zhang, T.; Xie, J.
Functional variant in methionine synthase reductase intron-1 is associated with pleiotropic congenital malformations (2015), Mol. Cell. Biochem., 407, 51-56 .

Search for more literature for 1.16.1.8

Cloned(Commentary)

Cloned (Comment)	Organism
gene MTRR, genotyping, and identification and mapping of single nucleotide polymorphisms	Homo sapiens

Organism

Organism	UniProt	Comment	Textmining
Homo sapiens	Q9UBK8	-	-

Synonyms

Synonyms	Comment	Organism
Methionine synthase reductase	-	Homo sapiens
MTRR	-	Homo sapiens

General Information

General Information	Comment	Organism
malfunction	analysis of correlations of single nucleotide polymorphisms and various malformation anomalies, overview	Homo sapiens

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Release 2023.1 (January 2023)