Genopathy
Gene-Disorder Association · Article
Gene
SLC4A1
Solute Carrier Family 4 Member 1 (Diego Blood Group)
Disorder
Renal Tubular Acidosis, Distal, 4, With Hemolytic Anemia
First reported 1998
Supporting publications 11
Key publication · gene–disorder Novel AE1 mutations in recessive distal renal tubular acidosis. Loss-of-function is rescued by glycophorin A.The Journal of clinical investigation · 1998
Key publication · disorder [Generalized saturnine paralysis. Discovery of a double congenital disease: glucose-6-phosphate dehydrogenase deficiency (new variant) and distal tubular acidosis].Annales de medecine interne · 1977
Manually curated
Association Review

In brief

The association between SLC4A1 (Solute Carrier Family 4 Member 1 (Diego Blood Group)) and Renal Tubular Acidosis, Distal, 4, With Hemolytic Anemia is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and a causative germline mutation.

Sources 5
Clinical variants 163
Symptoms 23
Compounds 0
Trials 0
Publications 11
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
SLC4A1

The gene

1 source summary

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

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04
Renal Tubular Acidosis, Distal, 4, With Hemolytic Anemia

The disorder

11 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

16 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

163 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

11 publications

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

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09
Provenance

References & sources

16 references

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

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