60S ribosomal protein L35

(Redirected from RPL35 (gene))

60S ribosomal protein L35 is a protein that in humans is encoded by the RPL35 gene.[5][6]

RPL35
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRPL35, L35, ribosomal protein L35, DBA19
External IDsOMIM: 618315; MGI: 1913739; HomoloGene: 31432; GeneCards: RPL35; OMA:RPL35 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_007209

NM_025592

RefSeq (protein)

NP_009140

NP_079868

Location (UCSC)Chr 9: 124.86 – 124.86 MbChr 2: 38.89 – 38.9 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

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Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L29P family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome.[6]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000136942Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000062997Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Uechi T, Tanaka T, Kenmochi N (Jun 2001). "A complete map of the human ribosomal protein genes: assignment of 80 genes to the cytogenetic map and implications for human disorders". Genomics. 72 (3): 223–30. doi:10.1006/geno.2000.6470. PMID 11401437.
  6. ^ a b "Entrez Gene: RPL35 ribosomal protein L35".
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Further reading

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