Basic Information

Symbol
RPS19
RNA class
mRNA
Alias
Ribosomal Protein S19 ES19 S19 DBA Loss Of Heterozygosity On Chromosome 19, Region 1 Loss Of Heterozygosity, 19, Chromosomal Region 1 Small Ribosomal Subunit Protein ES19 40S Ribosomal Protein S19 LOH19CR1 Diamond-Blackfan Anemia DBA1
Location (GRCh38)
Forensic tag(s)
Other applications

MANE select

Transcript ID
NM_001022.4
Sequence length
2021.0 nt
GC content
0.5596

Transcripts

ID Sequence Length GC content
CCCUUUCCCCUGGCUGGCAGCGCGGAGGCCGCACGAUGCCUGGAGUUAC… 2021 nt 0.5596
AGAGCCGCGGCCACGUGCGAGCGGCAGGCCCGGACAUGCCCGGUCAGCG… 2077 nt 0.5672
CCCUUUCCCCUGGCUGGCAGCGCGGAGGCCGCACGGUAAGCGGGGGCUC… 2177 nt 0.5774
CCCUUUCCCCUGGCUGGCAGCGCGGAGGCCGCACGAUGCCUGGAGUUAC… 2034 nt 0.5590
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. [provided by RefSeq, Jul 2008]

Forensic Context

A study in humans demonstrated that the RPS19 was listed among the top 15 most highly expressed housekeeping genes with a low coefficient of variation across individuals, indicating it exhibits low variation and appears insensitive to factors like genetics, environment, age, and gender [Sharma et al. DOI:10.1152/physiolgenomics.00228.2003].