Genopathy
Gene-Disorder Association · Article
Gene
LOC109610631
Aristaless Related Homeobox Polyalanine Expansion Region
Disorder
West Syndrome
First reported 1997
Supporting publications 38
Key publication · gene–disorder The X-linked infantile spasms syndrome (MIM 308350) maps to Xp11.4-Xpter in two pedigrees.Annals of neurology · 1997
Key publication · disorder Diagnosis and prognosis of hypsarhythmia and infantile spasms.Pediatrics · 1954
Manually curated
Association Review

In brief

The association between LOC109610631 (Aristaless Related Homeobox Polyalanine Expansion Region) and West Syndrome is well established and manually curated, drawing on a single expert-curated source, which records pathogenic and likely-pathogenic variants.

Sources 1
Clinical variants 131
Symptoms 7
Compounds 0
Trials 0
Publications 38
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
LOC109610631

The gene

1 source summary

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

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04
West Syndrome

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

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

131 clinical variants

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

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07
Literature

Reading

38 publications

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

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08
Provenance

References & sources

13 references

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

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