UBQLN2

UBQLN2
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauUBQLN2, ALS15, CHAP1, DSK2, N4BP4, PLIC2, HRIHFB2157, ubiquilin 2
Dynodwyr allanolOMIM: 300264 HomoloGene: 81830 GeneCards: UBQLN2
Patrwm RNA pattern
Rhagor o gyfeiriadau
Orthologau
SpeciesBod dynolLlygoden
Entrez

29978

n/a

Ensembl

ENSG00000188021

n/a

UniProt

Q9UHD9

n/a

RefSeq (mRNA)

NM_013444

n/a

RefSeq (protein)

NP_038472

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 UBQLN2 yw UBQLN2 a elwir hefyd yn Ubiquilin 2 (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 X dynol, band Xp11.21.[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 UBQLN2.

  • DSK2
  • ALS15
  • CHAP1
  • N4BP4
  • PLIC2
  • HRIHFB2157

Llyfryddiaeth

  • "Disturbance of proteasomal and autophagic protein degradation pathways by amyotrophic lateral sclerosis-linked mutations in ubiquilin 2. ". Biochem Biophys Res Commun. 2016. PMID 26944018.
  • "Ubiquilin2 as a novel marker for detection of urothelial carcinoma cells in urine. ". Diagn Cytopathol. 2016. PMID 26303000.
  • "No Evidence for Pathogenic Role of UBQLN2 Mutations in Sporadic Amyotrophic Lateral Sclerosis in the Mainland Chinese Population. ". PLoS One. 2017. PMID 28125704.
  • "Increased Ubqln2 expression causes neuron death in transgenic rats. ". J Neurochem. 2016. PMID 27456931.
  • "[Ubiquilin-2 immunostaining - a new marker as a diagnostic supplement in urine cytology?].". Urologe A. 2016. PMID 27168037.

Cyfeiriadau

  1. ↑ "Human PubMed Reference:".
  2. ↑ UBQLN2 - Cronfa NCBI

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