Genopathy
Gene-Disorder Association · Article
Gene
MIR659
MicroRNA 659
Disorder
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7
First reported 2008
Supporting publications 1
Key publication · gene–disorder Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia.Human molecular genetics · 2008
Key publication · disorder Amyotrophic lateral sclerosis.The Journal of nervous and mental disease · 1950
Manually curated
Association Review

In brief

The association between MIR659 (MicroRNA 659) and Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7 is reported, supported by a single source.

Sources 1
Clinical variants 0
Symptoms 107
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

1 source

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

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03
MIR659

The gene

1 source summary

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

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04
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7

The disorder

30 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

70 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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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

8 references

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

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