Gene-Disorder Association · Article
Gene
RPS19 Ribosomal Protein S19
×
First reported
1999
Supporting publications
58
Manually curated Approved treatment annotated
Association Review
In brief The association between RPS19 (Ribosomal Protein S19) and Diamond-Blackfan Anemia 1 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources
4
Clinical variants
234
Symptoms
79
Compounds
2
Trials
0 of 3,513 via RPS19 compounds
Publications
58
Contents
01
At a glance
Association overview A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.
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02
Provenance
Evidence and sources 4 sources
Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.
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1 source summary
A gene summary alongside the source descriptions it was distilled from.
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04
Diamond-Blackfan Anemia 1
The disorder 13 database identifiers
The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).
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05
Phenotype
Clinical features 55 clinical features
The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.
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06
ClinVar and variant evidence
Genetic basis 234 clinical variants
ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.
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07
Mechanism overlap
Shared mechanisms Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.
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08
Interventions
Therapeutics 2 compounds & drugs
Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.
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09
Human studies
Clinical trials 3,513 clinical trials
Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.
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58 publications
Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.
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11
Provenance
References & sources 15 references
Every source and publication cited across this dossier, as one numbered reference list.
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