Genopathy
Gene-Disorder Association · Article
Gene
LOC130059394
ATAC-STARR-Seq Lymphoblastoid Silent Region 7701
Disorder
Spastic Paraplegia 35, Autosomal Recessive, With Or Without Neurodegeneration
First reported 2010
Supporting publications 5
Key publication · gene–disorder Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35).Human mutation · 2010
Key publication · disorder New approaches in the management of hyperkinetic movement disorders.Advances in experimental medicine and biology · 1977
Manually curated
Association Review

In brief

The association between LOC130059394 (ATAC-STARR-Seq Lymphoblastoid Silent Region 7701) and Spastic Paraplegia 35, Autosomal Recessive, With Or Without Neurodegeneration is well established and manually curated, drawing on a single expert-curated source, which records pathogenic and likely-pathogenic variants.

Sources 1
Clinical variants 23
Symptoms 77
Compounds 0
Trials 0
Publications 5
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
LOC130059394

The gene

1 source summary

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

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04
Spastic Paraplegia 35, Autosomal Recessive, With Or Without Neurodegeneration

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

53 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

23 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

5 publications

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

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08
Provenance

References & sources

12 references

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

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