Methylenetetrahydrofolate reductase

MTHFR
Identifiers
AliasesMTHFR, entrez:4524, methylenetetrahydrofolate reductase
External IDsOMIM: 607093; MGI: 106639; HomoloGene: 4349; GeneCards: MTHFR; OMA:MTHFR - orthologs
Orthologs
SpeciesHumanMouse
Entrez

4524

17769

Ensembl

ENSG00000177000

ENSMUSG00000029009

UniProt

P42898

Q9WU20

RefSeq (mRNA)

NM_005957
NM_001330358

NM_001161798
NM_010840

RefSeq (protein)

NP_001317287
NP_005948

NP_001155270
NP_034970

Location (UCSC)Chr 1: 11.79 – 11.81 MbChr 4: 148.12 – 148.14 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Methylenetetrahydrofolate reductase (MTHFR) is the rate-limiting enzyme in the methyl cycle, and it is encoded by the MTHFR gene. Methylenetetrahydrofolate reductase catalyzes the conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate, a cosubstrate for homocysteine remethylation to methionine. Natural variation in this gene is common in otherwise healthy people. Although some variants have been reported to influence susceptibility to occlusive vascular disease, neural tube defects, Alzheimer's disease and other forms of dementia, colon cancer, and acute leukemia, findings from small early studies have not been reproduced. Some mutations in this gene are associated with methylenetetrahydrofolate reductase deficiency. Complex I deficiency with recessive spastic paraparesis has also been linked to MTHFR variants. In addition, the aberrant promoter hypermethylation of this gene is associated with male infertility and recurrent spontaneous abortion.