MTHFD1

Oddi ar Wicipedia
MTHFD1
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauMTHFD1, MTHFC, MTHFD, C1-THF-Synthase, methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1, CIMAH
Dynodwyr allanolOMIM: 172460 HomoloGene: 55940 GeneCards: MTHFD1
Patrwm RNA pattern
Rhagor o gyfeiriadau
Orthologau
SpeciesBod dynolLlygoden
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005956
NM_001364837

n/a

RefSeq (protein)

NP_005947
NP_001351766

n/a

Lleoliad (UCSC)n/an/a
PubMed search[1]n/a
Wicidata
Gweld/Golygu Bod dynol

Protein sy'n cael ei godio yn y corff dynol gan y genyn MTHFD1 yw MTHFD1 a elwir hefyd yn C-1-tetrahydrofolate synthase, cytoplasmic a Methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1 (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn blaen o gromosom dynol 14, band 14q23.3.[2]

Cyfystyron[golygu | golygu cod]

Yn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn MTHFD1.

  • CIMAH
  • MTHFC
  • MTHFD

Llyfryddiaeth[golygu | golygu cod]

  • "One-carbon genetic variants and the role of MTHFD1 1958G>A in liver and colon cancer risk according to global DNA methylation. ". PLoS One. 2017. PMID 28968444.
  • "Methylenetetrahydrofolate Dehydrogenase 1 Polymorphisms Modify the Associations of Plasma Glycine and Serine With Risk of Acute Myocardial Infarction in Patients With Stable Angina Pectoris in WENBIT (Western Norway B Vitamin Intervention Trial). ". Circ Cardiovasc Genet. 2016. PMID 27872106.
  • "MTHFD1 regulates nuclear de novo thymidylate biosynthesis and genome stability. ". Biochimie. 2016. PMID 26853819.
  • "B vitamin treatments modify the risk of myocardial infarction associated with a MTHFD1 polymorphism in patients with stable angina pectoris. ". Nutr Metab Cardiovasc Dis. 2016. PMID 26803590.
  • "Paternal transmission of MTHFD1 G1958A variant predisposes to neural tube defects in the offspring.". Dev Med Child Neurol. 2016. PMID 26394717.

Cyfeiriadau[golygu | golygu cod]

  1. "Human PubMed Reference:".
  2. MTHFD1 - Cronfa NCBI