Genopathy
Gene-Disorder Association · Article
Gene
SPG7
SPG7 Matrix AAA Peptidase Subunit, Paraplegin
Disorder
Hereditary Spastic Paraplegia
First reported 1998
Supporting publications 32
Key publication · gene–disorder Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease.Cell · 1998
Key publication · disorder Hereditary spastic paraplegia.Journal of neurology, neurosurgery, and psychiatry · 1950
Manually curated
Association Review

In brief

The association between SPG7 (SPG7 Matrix AAA Peptidase Subunit, Paraplegin) and Hereditary Spastic Paraplegia is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording pathogenic variants.

Sources 2
Clinical variants 72
Symptoms 3
Compounds 0
Trials 0
Publications 32
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

2 sources

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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03
SPG7

The gene

1 source summary

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

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04
Hereditary Spastic Paraplegia

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
ClinVar and variant evidence

Genetic basis

72 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

32 publications

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

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07
Provenance

References & sources

13 references

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

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