Genopathy
Gene-Disorder Association · Article
Gene
NEK1
NIMA Related Kinase 1
Disorder
Motor Neuron Disease
First reported 2017
Supporting publications 1
Key publication · gene–disorder Genetic epidemiology of motor neuron disease-associated variants in the Scottish population.Neurobiology of aging · 2017
Key publication · disorder [Bulbar syndrome; compression by occipital sequestrum; obstetrical trauma; secondary hydrocephalus].Anais paulistas de medicina e cirurgia · 1950
Manually curated
Association Review

In brief

The association between NEK1 (NIMA Related Kinase 1) and Motor Neuron Disease is well established and manually curated, with its 2 contributing sources — 1 of them expert-curated — recording likely-pathogenic variants.

Sources 2
Clinical variants 18
Symptoms 4
Compounds 0
Trials 0
Publications 1
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
NEK1

The gene

1 source summary

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

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04
Motor Neuron Disease

The disorder

9 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

18 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

1 publication

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

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07
Provenance

References & sources

5 references

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

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