About: RPS19 wt Allele     Goto   Sponge   Distinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • RPS19 wt Allele
equivalentClass
OMIM_Number
  • 603474
GenBank_Accession_Number
  • NM_001022
Semantic_Type
  • Gene or Genome
Preferred_Name
  • RPS19 wt Allele
UMLS_CUI
  • C1706158
GO_Annotation
  • RNA bindingGO:0003723TAS29-SEP-2003CGAP
  • hemocyte developmentGO:0007516TAS29-SEP-2003CGAP
  • protein biosynthesisGO:0006412TAS29-SEP-2003CGAP
  • structural constituent of ribosomeGO:0003735TAS29-SEP-2003CGAP
  • cytosolic small ribosomal subunit (sensu Eukarya)GO:0005843TAS29-SEP-2003CGAP
EntrezGene_ID
  • 6223
Legacy_Concept_Name
  • RPS19_wt_Allele
HGNC_ID
  • HGNC:10402
FULL_SYN
  • DBASYNCI
  • RPS19 wt AllelePTNCI
  • Ribosomal Protein S19 wt AlleleSYNCI
Gene_Encodes_Product
  • Ribosomal Protein S19
DEFINITION
  • Human RPS19 wild-type allele is located in the vicinity of 19q13.2 and is approximately 11 kb in length. This allele, which encodes 40S ribosomal protein S19, may play a role in both erythrocyte differentiation and protein synthesis. Mutations that result in the expression of a truncated gene are associated with Diamond-Blackfan anemia. Aberrant elevated expression of this gene is associated with some colon carcinomas.NCI
DesignNote
  • 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. The RPS19 gene encodes a ribosomal protein that is a component of the 40S subunit. (Entrez Gene)
code
  • C53162
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