Gene-Disorder Association · Article
Gene
SLC11A2 Solute Carrier Family 11 Member 2
×
First reported
1999
Supporting publications
8
Manually curated Approved treatment annotated
Association Review
In brief The association between SLC11A2 (Solute Carrier Family 11 Member 2) and Protein-Deficiency Anemia is reported, with clinical genetic testing available.
Sources
1
Clinical variants
0
Symptoms
3
Compounds
1
Trials
0 of 10 via SLC11A2 compounds
Publications
8
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 1 source
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
Protein-Deficiency Anemia
The disorder 20 database identifiers
The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).
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05
Interventions
Therapeutics 1 compound or drug
Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.
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06
Human studies
Clinical trials 10 clinical trials
Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.
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8 publications
Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.
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08
Provenance
References & sources 12 references
Every source and publication cited across this dossier, as one numbered reference list.
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