Genopathy
Gene-Disorder Association · Article
Gene
STON1-GTF2A1L
STON1-GTF2A1L Readthrough
Disorder
Leydig Cell Hypoplasia Type Ii
First reported 1997
Supporting publications 3
Key publication · disorder Comparison of immunocytochemical and molecular features with the phenotype in a case of incomplete male pseudohermaphroditism associated with a mutation of the luteinizing hormone receptor.The Journal of clinical endocrinology and metabolism · 1997
Association Review

In brief

The association between STON1-GTF2A1L (STON1-GTF2A1L Readthrough) and Leydig Cell Hypoplasia Type Ii is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 3
Symptoms 0
Compounds 0
Trials 0
Publications 3
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
STON1-GTF2A1L

The gene

1 source summary

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

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04
Leydig Cell Hypoplasia Type Ii

The disorder

6 database identifiers

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

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05
ClinVar and variant evidence

Genetic basis

3 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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06
Literature

Reading

3 publications

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

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07
Provenance

References & sources

6 references

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

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