WD repeat domain 18

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

WD repeat domain 18 is a protein that in humans is encoded by the WDR18 gene. [5]

AliasesWDR18, Ipi3, R32184_1, WD repeat domain 18
End998,438 bp[1]
Quick facts WDR18, Identifiers ...
WDR18
Identifiers
AliasesWDR18, Ipi3, R32184_1, WD repeat domain 18
External IDsMGI: 2158400; HomoloGene: 32573; GeneCards: WDR18; OMA:WDR18 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_024100
NM_001372085
NM_001372086

NM_175450

RefSeq (protein)

NP_077005
NP_001359014
NP_001359015

NP_780659

Location (UCSC)Chr 19: 0.98 – 1 MbChr 10: 79.8 – 79.81 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. WDR18 forms a nucleolar complex with LAS1L, PELP1, TEX10 called the rixosome which is involved in RNA degradation.[6][7] The rixosome is a nucleolar complex that cofractionates with the 60S preribosomal subunit. Recruitment of the rixosome by the Polycomb Repressive Complex 1 has been proposed to lead to its functioning in establishing repressive chromatin structures by assisting in degrading nascent RNA.[8]

References

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