LMNB1

2KPW, 3JT0, 3TYY, 3UMN

LMNB1
LMNB1
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauLMNB1, ADLD, LMN, LMN2, LMNB, lamin B1, MCPH26
Dynodwyr allanolOMIM: 150340 HomoloGene: 55912 GeneCards: LMNB1
Patrwm RNA pattern
Rhagor o gyfeiriadau
Orthologau
SpeciesBod dynolLlygoden
Entrez

4001

n/a

Ensembl

ENSG00000113368

n/a

UniProt

P20700

n/a

RefSeq (mRNA)

NM_001198557
NM_005573

n/a

RefSeq (protein)

NP_001185486
NP_005564

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 LMNB1 yw LMNB1 a elwir hefyd yn Lamin B1 (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 5, band 5q23.2.[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 LMNB1.

  • LMN
  • ADLD
  • LMN2
  • LMNB

Llyfryddiaeth

  • "Nuclear envelope rupture is induced by actin-based nucleus confinement.". J Cell Biol. 2016. PMID 27697922.
  • Autosomal Dominant Leukodystrophy with Autonomic Disease. 1993. PMID 26749591.
  • "Defects of Lipid Synthesis Are Linked to the Age-Dependent Demyelination Caused by Lamin B1 Overexpression.". J Neurosci. 2015. PMID 26311780.
  • "LMNB1-related autosomal-dominant leukodystrophy: Clinical and radiological course.". Ann Neurol. 2015. PMID 26053668.
  • "Regulation of homologous recombinational repair by lamin B1 in radiation-induced DNA damage.". FASEB J. 2015. PMID 25733566.

Cyfeiriadau

  1. ↑ "Human PubMed Reference:".
  2. ↑ LMNB1 - Cronfa NCBI

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