UBXN4

2KXJ

UBXN4
UBXN4
Strwythurau
PDBHuman UniProt search: PDBe RCSB
Dynodwyr
CyfenwauUBXN4, UBXD2, UBXDC1, erasin, UBX domain protein 4
Dynodwyr allanolOMIM: 611216 HomoloGene: 40962 GeneCards: UBXN4
Patrwm RNA pattern




Rhagor o gyfeiriadau
Orthologau
SpeciesBod dynolLlygoden
Entrez

23190

n/a

Ensembl

ENSG00000144224

n/a

UniProt

Q92575

n/a

RefSeq (mRNA)

NM_014607

n/a

RefSeq (protein)

NP_055422

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 UBXN4 yw UBXN4 a elwir hefyd yn UBX domain protein 4 (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 2, band 2q21.3.[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 UBXN4.

  • UBXD2
  • UBXDC1
  • erasin

Llyfryddiaeth

  • "SEL1L nucleates a protein complex required for dislocation of misfolded glycoproteins. ". Proc Natl Acad Sci U S A. 2008. PMID 18711132.
  • "Ubiquilin and p97/VCP bind erasin, forming a complex involved in ERAD. ". J Cell Biol. 2009. PMID 19822669.
  • "A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. ". Hum Mol Genet. 2012. PMID 21979947.
  • "Characterization of erasin (UBXD2): a new ER protein that promotes ER-associated protein degradation. ". J Cell Sci. 2006. PMID 16968747.
  • "Human ASPL/TUG interacts with p97 and complements the proteasome mislocalization of a yeast ubx4 mutant, but not the ER-associated degradation defect.". BMC Cell Biol. 2014. PMID 25078495.

Cyfeiriadau

  1. ↑ "Human PubMed Reference:".
  2. ↑ UBXN4 - Cronfa NCBI

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