Genopathy
Gene-Disorder Association · Article
Gene
SLC25A32
Solute Carrier Family 25 Member 32
Disorder
Glutamate Formiminotransferase Deficiency
First reported 1963
Key publication · disorder Formiminoglutamicaciduria in humans with megaloblastic anemia: diminution by methionine or glycine.Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.) · 1963
Manually curated
Association Review

In brief

The association between SLC25A32 (Solute Carrier Family 25 Member 32) and Glutamate Formiminotransferase Deficiency is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 26
Compounds 0
Trials 0
Publications 0
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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03
SLC25A32

The gene

1 source summary

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

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04
Glutamate Formiminotransferase Deficiency

The disorder

10 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

19 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
Provenance

References & sources

6 references

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

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