MTRR Chromosome 5

5-methyltetrahydrofolate-homocysteine methyltransferase reductase
139 variants 139 Health Risk

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What This Gene Does
This gene encodes a member of the ferredoxin-NADP(+) reductase (FNR) family of electron transferases. This protein functions in the synthesis of methionine by regenerating methionine synthase to a functional state. Because methionine synthesis requires methyl-group transfer by a folate donor, activity of the encoded enzyme is important for folate metabolism and cellular methylation. Mutations in this gene can cause homocystinuria-megaloblastic anemia, cbl E type. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]
Gene Info
Gene Group
Flavoproteins
Locus Type
gene with protein product
Location
5p15.31
Ensembl
ENSG00000124275
Associated Conditions (9)
Methylcobalamin deficiency type cblE
Disorders of Intracellular Cobalamin Metabolism
MTRR-related disorder
Neural tube defects
folate-sensitive
Methylcobalamin deficiency type cblG
Inborn genetic diseases
Colon adenocarcinoma
Homocystinuria without methylmalonic aciduria
Key Variants
RS114748706
Conflicting classifications of pathogenicity
Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism, MTRR-related disorder
Health Risk
RS12347
Conflicting classifications of pathogenicity
Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE
Health Risk
RS1254913477
Conflicting classifications of pathogenicity
Methylcobalamin deficiency type cblE, Neural tube defects, folate-sensitive
Health Risk
RS140944718
Conflicting classifications of pathogenicity
Methylcobalamin deficiency type cblE, Inborn genetic diseases, Methylcobalamin deficiency type cblE
Health Risk
RS142714881
Conflicting classifications of pathogenicity
Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
Health Risk
RS143418731
Conflicting classifications of pathogenicity
Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism
Health Risk
RS144899305
Conflicting classifications of pathogenicity
Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Inborn genetic diseases
Health Risk
RS148909799
Conflicting classifications of pathogenicity
Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, MTRR-related disorder
Health Risk
RS149037732
Conflicting classifications of pathogenicity
Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE
Health Risk
RS149300444
Conflicting classifications of pathogenicity
Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE
Health Risk
RS149678769
Conflicting classifications of pathogenicity
Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Inborn genetic diseases
Health Risk
RS150411351
Conflicting classifications of pathogenicity
Methylcobalamin deficiency type cblE, Neural tube defects, folate-sensitive
Health Risk
All Variants (139)
RSID Category Clinical Significance Conditions
RS114748706 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism, MTRR-related disorder
RS12347 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE
RS1254913477 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Neural tube defects, folate-sensitive
RS140944718 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Inborn genetic diseases, Methylcobalamin deficiency type cblE
RS142714881 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
RS143418731 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism
RS144899305 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Inborn genetic diseases
RS148909799 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, MTRR-related disorder
RS149037732 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE
RS149300444 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE
RS149678769 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Inborn genetic diseases
RS150411351 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Neural tube defects, folate-sensitive
RS200661044 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism
RS202110383 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Inborn genetic diseases
RS368193742 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Disorders of Intracellular Cobalamin Metabolism
RS368391537 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism
RS375332745 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Inborn genetic diseases, Methylcobalamin deficiency type cblE
RS560321328 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism
RS577851734 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism
RS746404785 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Inborn genetic diseases, Methylcobalamin deficiency type cblE
RS750381895 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
RS753947379 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism
RS757184514 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism
RS796052001 Health Risk Conflicting classifications of pathogenicity Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
RS886060807 Health Risk Conflicting classifications of pathogenicity Disorders of Intracellular Cobalamin Metabolism, Methylcobalamin deficiency type cblE, Disorders of Intracellular Cobalamin Metabolism
RS1181934270 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
RS1189298981 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Neural tube defects, folate-sensitive
RS1212701617 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Neural tube defects, folate-sensitive
RS1219605974 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
RS1400065323 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Neural tube defects, folate-sensitive
RS143058455 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
RS1532268 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
RS1734858651 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Neural tube defects, folate-sensitive
RS1737148739 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
RS1737854315 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
RS1738695332 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
RS1748331186 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
RS1748371268 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
RS1748372023 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
RS1748694912 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Methylcobalamin deficiency type cblE
RS2126645870 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
RS2126676051 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
RS2126692827 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
RS2126808287 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Neural tube defects, folate-sensitive
RS2476220505 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
RS2478648157 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Methylcobalamin deficiency type cblE
RS2478700578 Health Risk Likely pathogenic Methylcobalamin deficiency type cblE, Methylcobalamin deficiency type cblE
RS2478705556 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
RS2478742432 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
RS2478742839 Health Risk Likely pathogenic Neural tube defects, folate-sensitive, Neural tube defects
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