Genopathy
Gene-Disorder Association · Article
Gene
CACNA1F
Calcium Voltage-Gated Channel Subunit Alpha1 F
Disorder
Cone-Rod Dystrophy, X-Linked, 3
First reported 2006
Supporting publications 9
Key publication · gene–disorder X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.Journal of medical genetics · 2006
Key publication · disorder Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3.Genomics · 1993
Manually curated
Association Review

In brief

The association between CACNA1F (Calcium Voltage-Gated Channel Subunit Alpha1 F) and Cone-Rod Dystrophy, X-Linked, 3 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 3
Clinical variants 27
Symptoms 29
Compounds 0
Trials 0
Publications 9
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
CACNA1F

The gene

2 source summaries

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

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04
Cone-Rod Dystrophy, X-Linked, 3

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

14 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

27 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

9 publications

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

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09
Provenance

References & sources

14 references

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

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