Genopathy
Gene-Disorder Association · Article
Gene
KCNMA1
Potassium Calcium-Activated Channel Subfamily M Alpha 1
Disorder
Cerebellar Atrophy, Developmental Delay, And Seizures
First reported 2016
Supporting publications 3
Key publication · gene–disorder Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizures.Human genetics · 2016
Key publication · disorder Maximal clarity on neurodevelopmental disorders.Developmental medicine and child neurology · 1968
Manually curated
Association Review

In brief

The association between KCNMA1 (Potassium Calcium-Activated Channel Subfamily M Alpha 1) and Cerebellar Atrophy, Developmental Delay, And Seizures is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and likely-pathogenic variants.

Sources 3
Clinical variants 29
Symptoms 22
Compounds 0
Trials 0
Publications 3
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

3 sources

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

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03
KCNMA1

The gene

2 source summaries

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

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04
Cerebellar Atrophy, Developmental Delay, And Seizures

The disorder

7 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

7 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

29 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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07
Mechanism overlap

Shared mechanisms

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

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08
Literature

Reading

3 publications

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

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09
Provenance

References & sources

9 references

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

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