Genopathy
Gene-Disorder Association · Article
Gene
KCNH5
Potassium Voltage-Gated Channel Subfamily H Member 5
Disorder
Lissencephaly Due To Lis1 Mutation
First reported 1982
Key publication · disorder Isolation and partial characterization of the sialoglycoprotein fraction of murine erythrocyte ghosts.The Journal of cell biology · 1982
Manually curated
Association Review

In brief

The association between KCNH5 (Potassium Voltage-Gated Channel Subfamily H Member 5) and Lissencephaly Due To Lis1 Mutation is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 47
Compounds 0
Trials 0
Publications 0
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
KCNH5

The gene

2 source summaries

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

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04
Lissencephaly Due To Lis1 Mutation

The disorder

5 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

44 clinical features

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

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06
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

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07
Provenance

References & sources

6 references

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

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