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RPS19

Gene

ribosomal protein S19

HGNCHGNC:10402EnsemblENSG00000105372NCBI Gene6223
Locus: gene with protein productLocation: 19q13.2

Encodes

via encodes

The protein product this gene encodes, reached through the canonical GENE→PROTEIN (encodes) relation. Its biology, drugs, indications, trials and therapeutic evidence live on the protein's own page.

Small ribosomal subunit protein eS19P39019

Protein · therapeutic target

Clinically validated target · 1 approved medicine against this target

Explore protein biology & therapeutics

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asLOH19CR1 · S19 · eS19 · DBA
View full nomenclature history (7)
Previous symbolsLOH19CR1
Alias symbolsS19, eS19, DBA
Previous namesloss of heterozygosity on chromosome 19, region 1, loss of heterozygosity, 19, chromosomal region 1
Alias namesDiamond-Blackfan anemia

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Muscular Dystrophy, Duchenne
Influenza, Human
Severe Acute Respiratory Syndrome

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

S ribosomal proteinsMicroRNA protein coding host genes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.