Exosome component 3

EXOSC3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
Aliases EXOSC3, PCH1B, RRP40, Rrp40p, bA3J10.7, hRrp-40, p10, CGI-102, Exosome component 3
External IDs MGI: 1913612 HomoloGene: 6867 GeneCards: EXOSC3
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

51010

66362

Ensembl

ENSG00000107371

ENSMUSG00000028322

UniProt

Q9NQT5

Q7TQK4

RefSeq (mRNA)

NM_016042
NM_001002269

NM_025513

RefSeq (protein)

NP_001002269.1
NP_057126.2

NP_079789.1

Location (UCSC) Chr 9: 37.77 – 37.8 Mb Chr 4: 45.32 – 45.34 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

Exosome component 3, also known as EXOSC3, is a human gene, which is part of the exosome complex.[3]

Clinical significance

Mutations in EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.[4]

References

  1. "Human PubMed Reference:".
  2. "Mouse PubMed Reference:".
  3. "Entrez Gene: EXOSC3 exosome component 3".
  4. Wan J, Yourshaw M, Mamsa H, Rudnik-Schöneborn S, Menezes MP, Hong JE, Leong DW, Senderek J, Salman MS, Chitayat D, Seeman P, von Moers A, Graul-Neumann L, Kornberg AJ, Castro-Gago M, Sobrido MJ, Sanefuji M, Shieh PB, Salamon N, Kim RC, Vinters HV, Chen Z, Zerres K, Ryan MM, Nelson SF, Jen JC (2012). "Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration". Nat. Genet. 44 (6): 704–8. doi:10.1038/ng.2254. PMC 3366034Freely accessible. PMID 22544365.

Further reading


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