MTR (5-methyltetrahydrofolate-homocysteine methyltransferase)

2007-02-01  

Identity

HGNC
LOCATION
1q43
LOCUSID
ALIAS
HMAG,MS,cblG
FUSION GENES

Other Information

Locus ID:

NCBI: 4548
MIM: 156570
HGNC: 7468
Ensembl: ENSG00000116984

Variants:

dbSNP: 4548
ClinVar: 4548
TCGA: ENSG00000116984
COSMIC: MTR

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000116984ENST00000366576B1ANE3
ENSG00000116984ENST00000366577Q99707
ENSG00000116984ENST00000535889Q99707
ENSG00000116984ENST00000650888A0A494C064
ENSG00000116984ENST00000651455A0A494C1A2

Expression (GTEx)

0
5
10
15
20
25
30
35
40

Pathways

PathwaySourceExternal ID
Selenocompound metabolismKEGGko00450
One carbon pool by folateKEGGko00670
Selenocompound metabolismKEGGhsa00450
One carbon pool by folateKEGGhsa00670
Cysteine and methionine metabolismKEGGko00270
Cysteine and methionine metabolismKEGGhsa00270
Metabolic pathwaysKEGGhsa01100
Biosynthesis of amino acidsKEGGhsa01230
Biosynthesis of amino acidsKEGGko01230
DiseaseREACTOMER-HSA-1643685
Diseases of metabolismREACTOMER-HSA-5668914
Defects in vitamin and cofactor metabolismREACTOMER-HSA-3296482
Defects in cobalamin (B12) metabolismREACTOMER-HSA-3296469
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblEREACTOMER-HSA-3359467
Defective MTR causes methylmalonic aciduria and homocystinuria type cblGREACTOMER-HSA-3359469
MetabolismREACTOMER-HSA-1430728
Metabolism of vitamins and cofactorsREACTOMER-HSA-196854
Metabolism of water-soluble vitamins and cofactorsREACTOMER-HSA-196849
Cobalamin (Cbl, vitamin B12) transport and metabolismREACTOMER-HSA-196741
Metabolism of amino acids and derivativesREACTOMER-HSA-71291
Sulfur amino acid metabolismREACTOMER-HSA-1614635
Biological oxidationsREACTOMER-HSA-211859
Phase II conjugationREACTOMER-HSA-156580
MethylationREACTOMER-HSA-156581

Protein levels (Protein atlas)

Not detected
Low
Medium
High

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA443297AgranulocytosisDiseaseClinicalAnnotationassociatedPD24712521
PA443553Brain DiseasesDiseaseVariantAnnotationassociatedPD17855192
PA445062NeoplasmsDiseaseClinicalAnnotationassociatedPD19159907, 21605004, 29662106
PA447288Essential hypertensionDiseaseClinicalAnnotationassociatedPD15148588
PA448561benazeprilChemicalClinicalAnnotationassociatedPD15148588
PA448803carboplatinChemicalClinicalAnnotationassociatedPD19159907, 21605004, 29662106
PA449014cisplatinChemicalClinicalAnnotationassociatedPD19159907, 21605004, 29662106
PA450428methotrexateChemicalClinicalAnnotation, VariantAnnotationambiguousPKPD15797993, 16013960, 17611986, 17855192, 18322994, 19159907, 22838948, 24712521, 27217051, 27676277

References

Pubmed IDYearTitleCitations
383258322024Genetic Association between the Risk of Dental Caries and MTR Gene Polymorphism in Chinese Children.0
383258322024Genetic Association between the Risk of Dental Caries and MTR Gene Polymorphism in Chinese Children.0
372490732023Association of MTR A2756G and MTRR A66G Polymorphisms With Male Infertility: An Updated Meta-Analysis.0
372963032023Association of MTR gene polymorphisms with the occurrence of non-syndromic congenital heart disease: a case-control study.1
375315122023Association of MTR and MTRR genes and oral health-related quality of life in children with dental caries.0
376287522023Common Variants in One-Carbon Metabolism Genes (MTHFR, MTR, MTHFD1) and Depression in Gynecologic Cancers.0
372490732023Association of MTR A2756G and MTRR A66G Polymorphisms With Male Infertility: An Updated Meta-Analysis.0
372963032023Association of MTR gene polymorphisms with the occurrence of non-syndromic congenital heart disease: a case-control study.1
375315122023Association of MTR and MTRR genes and oral health-related quality of life in children with dental caries.0
376287522023Common Variants in One-Carbon Metabolism Genes (MTHFR, MTR, MTHFD1) and Depression in Gynecologic Cancers.0
333456882022MTR-G is a high-risk allele for lower-extremity arteriosclerotic occlusion.1
353327812022Folate metabolism abnormalities in infertile patients with endometriosis.1
354687342022"Association of MTHFR and MS/MTR gene polymorphisms with congenital heart defects in North Indian population (Jammu and Kashmir): a case-control study encompassing meta-analysis and trial sequential analysis".1
357156012022Investigation of the relationship between MTRR A66G, MTR A2756G gene variations and cell anomalies in early diagnosis and progression of bladder cancer.0
358026412022Association between MTR A2756G polymorphism and susceptibility to congenital heart disease: A meta-analysis.0

Citation

Dessen P

MTR (5-methyltetrahydrofolate-homocysteine methyltransferase)

Atlas Genet Cytogenet Oncol Haematol. 2007-02-01

Online version: http://atlasgeneticsoncology.org/gene/43820/js/gene-fusions-explorer/