Browse our RPS19 Proteins (RPS19)

Full name:
Ribosomal Protein S19 Proteins (RPS19)
On are 23 Ribosomal Protein S19 (RPS19) Proteins from 5 different suppliers available. Additionally we are shipping RPS19 Antibodies (96) and RPS19 Kits (14) and many more products for this protein. A total of 140 RPS19 products are currently listed.
DBA, DBA1, Dsk3, S19
list all proteins Gene Name GeneID UniProt
RPS19 6223 P39019
RPS19 20085 Q9CZX8
RPS19 29287 P17074

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RPS19 Proteins (RPS19) by Origin

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Human Ribosomal Protein S19 (RPS19) interaction partners

  1. Reducing RPS19 in tumor cells or blocking the C5a receptor 1-RPS19 interaction decreases RPS19-mediated immunosuppression, impairs tumor growth, and delays the development of tumors in a transgenic model of breast cancer

  2. RPS19-downregulated erythroleukemia cells show reduced FLVCR1a and FLVCR1b mRNA levels associated with heme overload.

  3. Loss of RPS19 expression is associated with Diamond-Blackfan anemia.

  4. Mutations R62W and R101H impair RPS19 ability to associate with the ribosome.

  5. Data indicate that GATA1 (show GATA1 Proteins) transcription factor is downregulated in ribosomal protein S19 (RPS19)-deficient cells through upregulation of TNF-alpha (show TNF Proteins) and p38 MAPK (show MAPK14 Proteins).

  6. RPS19 mutation is associated with Diamond Blackfan Anemia.

  7. A binding domain for RPS19 was identified and characterized in the N-terminus.

  8. increase of autophagy in cells derived from DBA patients, in CD34 (show CD34 Proteins)+ erythrocyte progenitor cells with RPS19 knock down, in the red blood cells of zebrafish embryos with RP-deficiency, and in cells from patients with Shwachman-Diamond syndrome

  9. levels of branched-chain aminotransferase-1 (BCAT1 (show BCAT1 Proteins)) transcripts are significantly decreased on the polysomes of both RPS19 and RPL11 (show RPL11 Proteins) cells and that translation of BCAT1 (show BCAT1 Proteins) protein is especially impaired in cells with small RP gene mutations

  10. High frequency of RPS19 gene deletion is associated with Italian Diamond-Blackfan anemia.

Mouse (Murine) Ribosomal Protein S19 (RPS19) interaction partners

  1. Mutation of the key residue for extraribosomal function of ribosomal protein S19 cause increased grooming behaviors in mice. Results suggest an involvement of RP S19 (show ASAP1 Proteins) oligomers in some anxiety-like behavior, especially grooming behavior.

  2. Rps19 mutant shows behavioural phenotypes resembling that of the human Diamond-Blackfan anaemia syndrome.

  3. indicate the importance of the RP S19 (show ASAP1 Proteins) oligomer-induced macrophage recruitment in coagulum resorption

  4. Rps19 mutant embryonic stem cells showed significant increase in p53 (show TP53 Proteins) protein expression.

  5. We report the generation of mouse models for RPS19-deficient Diamond Blackfan anemia using transgenic RNA interference that allows an inducible and graded down-regulation of Rps19.

  6. generated a transgenic model expressing an RPS19 mutation in which an arginine residue is replaced with a tryptophan residue at codon 62 as a model of Diamond-Blackfan anemia

  7. Combined Rps19 insufficiency and Pim-1 (show PIM1 Proteins) deficiency promote murine myeloid cell growth through a deregulation of c-Myc (show MYC Proteins) and a simultaneous up-regulation of anti-apoptotic Bcl proteins.

  8. RPS19 mRNA and protein expression were shown to decrease during terminal erythroid differentiation.

  9. Results indicate that ribosomal protein S19 (-/-) zygotes do not form blastocysts, whereas one normal Rps19 allele in mice is sufficient to maintain normal ribosomal and possibly extraribosomal functions.

  10. presence of an RP S19 (show ASAP1 Proteins) dimer- and C5a receptor-mediated autocrine-type augmentation mechanism during Mn II-induced apoptosis in the mouse fibroblastic cell line

RPS19 Protein Profile

Protein Summary

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 40S subunit. The protein belongs to the S19E family of ribosomal proteins. It is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia (DBA), a constitutional erythroblastopenia characterized by absent or decreased erythroid precursors, in a subset of patients. This suggests a possible extra-ribosomal function for this gene in erythropoietic differentiation and proliferation, in addition to its ribosomal function. Higher expression levels of this gene in some primary colon carcinomas compared to matched normal colon tissues has been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome.

Alternative names and synonyms associated with RPS19

  • 30S ribosomal protein S19 (rps19)
  • Protein RPS-19 (rps-19)
  • ribosomal protein S19 (RPS19)
  • ribosomal protein S19 (Rps19)
  • DBA protein
  • DBA1 protein
  • Dsk3 protein
  • S19 protein

Protein level used designations for Ribosomal Protein S19 Proteins (RPS19)

ribosomal protein S19 , 40S ribosomal protein S19

801541 Cyanophora paradoxa
2715642 Spinacia oleracea
172805 Caenorhabditis elegans
6223 Homo sapiens
476450 Canis lupus familiaris
516063 Bos taurus
20085 Mus musculus
29287 Rattus norvegicus
100169962 Felis catus
100173042 Pongo abelii
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