Genopathy
Gene-Disorder Association · Article
Gene
SLC11A2
Solute Carrier Family 11 Member 2
Disorder
Anemia, Hypochromic Microcytic, With Iron Overload 1
First reported 2005
Supporting publications 4
Key publication · gene–disorder Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload.Blood · 2005
Key publication · disorder [Increased lead absorption due to pica in a boy of seven, with achylia gastrica and hypochromic microcytic anemia].Maandschrift voor kindergeneeskunde · 1953
Manually curated
Association Review

In brief

The association between SLC11A2 (Solute Carrier Family 11 Member 2) and Anemia, Hypochromic Microcytic, With Iron Overload 1 is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.

Sources 5
Clinical variants 97
Symptoms 10
Compounds 0
Trials 0
Publications 4
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

5 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
SLC11A2

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

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04
Anemia, Hypochromic Microcytic, With Iron Overload 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

6 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

97 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
Literature

Reading

4 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

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09
Provenance

References & sources

12 references

Every source and publication cited across this dossier, as one numbered reference list.

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