AUTS2 and Microcephaly: Association Evidence

Gene-Disorder Association · Article

Gene

AUTS2

Activator Of Transcription And Developmental Regulator AUTS2

Disorder

First reported 1950

Key publication · disorder [Diffuse symmetric calcification in a syndrome including microcephaly and meningoencephalitis].Archiv fur Psychiatrie und Nervenkrankheiten, vereinigt mit Zeitschrift fur die gesamte Neurologie und Psychiatrie · 1950

Association Review

In brief

The association between AUTS2 (Activator Of Transcription And Developmental Regulator AUTS2) and Microcephaly is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1

Clinical variants 0

Symptoms 0

Compounds 0

Trials 0

Publications 0

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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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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AUTS2

The gene

1 source summary

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

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Microcephaly

The disorder

7 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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Provenance

References & sources

2 references

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

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