RUNX1

1CMO, 1CO1, 1E50, 1H9D, 1LJM

RUNX1
RUNX1
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauRUNX1, AML1, AML1-EVI-1, AMLCR1, CBF2alpha, CBFA2, EVI-1, PEBP2aB, PEBP2alpha, runt related transcription factor 1, RUNX family transcription factor 1
Dynodwyr allanolOMIM: 151385 HomoloGene: 1331 GeneCards: RUNX1
Patrwm RNA pattern




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

NM_001001890
NM_001122607
NM_001754

n/a

RefSeq (protein)

NP_001001890
NP_001116079
NP_001745

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 RUNX1 yw RUNX1 a elwir hefyd yn Runt related transcription factor 1 (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl o gromosom dynol 21, band 21q22.12.[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 RUNX1.

  • AML1
  • CBFA2
  • EVI-1
  • AMLCR1
  • PEBP2aB
  • CBF2alpha
  • AML1-EVI-1
  • PEBP2alpha

Llyfryddiaeth

  • "RUNX1 Upregulation by Cytotoxic Drugs Promotes Apoptosis. ". Cancer Res. 2017. PMID 29055018.
  • "Frequency and Clinicopathologic Features of RUNX1 Mutations in Patients With Acute Myeloid Leukemia Not Otherwise Specified. ". Am J Clin Pathol. 2017. PMID 28927163.
  • "H3K27M/I mutations promote context-dependent transformation in acute myeloid leukemia with RUNX1alterations. ". Blood. 2017. PMID 28855157.
  • "Myeloid neoplasms with germ line RUNX1 mutation. ". Int J Hematol. 2017. PMID 28534116.
  • "Recurrent somatic JAK-STAT pathway variants within a RUNX1-mutated pedigree.". Eur J Hum Genet. 2017. PMID 28513614.

Cyfeiriadau

  1. "Human PubMed Reference:".
  2. RUNX1 - Cronfa NCBI

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