FOXO3

2K86, 2LQH, 2LQI, 2UZK

FOXO3
FOXO3
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauFOXO3, AF6q21, FKHRL1, FKHRL1P2, FOXO2, FOXO3A, forkhead box O3
Dynodwyr allanolOMIM: 602681 HomoloGene: 31039 GeneCards: FOXO3
Patrwm RNA pattern




Rhagor o gyfeiriadau
Orthologau
SpeciesBod dynolLlygoden
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001455
NM_201559

n/a

RefSeq (protein)

NP_001446
NP_963853

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 FOXO3 yw FOXO3 a elwir hefyd yn Forkhead box O3 (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 6, band 6q21.[2]

Cyfystyron

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 FOXO3.

  • FOXO2
  • AF6q21
  • FKHRL1
  • FOXO3A
  • FKHRL1P2

Llyfryddiaeth

  • "Association of genetic variations in FOXO3 gene with susceptibility to noise induced hearing loss in a Chinese population. ". PLoS One. 2017. PMID 29220389.
  • "An intronic single-nucleotide polymorphism (rs13217795) in FOXO3 is associated with asthma and allergic rhinitis: a case-case-control study. ". BMC Med Genet. 2017. PMID 29141605.
  • "Investigation of FoxO3 dynamics during erythroblast development in β-thalassemia major. ". PLoS One. 2017. PMID 29099866.
  • "Protein kinase C downregulation induces senescence via FoxO3a inhibition in HCT116 and HEK293 cells. ". Biochem Biophys Res Commun. 2017. PMID 28989024.
  • "Chromosome 6q deletion correlates with poor prognosis and low relative expression of FOXO3 in chronic lymphocytic leukemia patients.". Am J Hematol. 2017. PMID 28699185.

Cyfeiriadau

  1. "Human PubMed Reference:".
  2. FOXO3 - Cronfa NCBI

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