Genopathy
Gene-Disorder Association · Article
Gene
MVP-DT
MVP Divergent Transcript
Disorder
Seizures, Benign Familial Infantile, 2
First reported 1997
Supporting publications 21
Key publication · gene–disorder Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.Epilepsia · 1997
Key publication · disorder Benign familial neonatal seizures: clinical and electroencephalographic characteristics.Pediatric neurology · 1986
Manually curated
Association Review

In brief

The association between MVP-DT (MVP Divergent Transcript) and Seizures, Benign Familial Infantile, 2 is well established and manually curated, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 42
Symptoms 11
Compounds 0
Trials 0
Publications 21
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
MVP-DT

The gene

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

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04
Seizures, Benign Familial Infantile, 2

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

5 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

42 clinical variants

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

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07
Literature

Reading

21 publications

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

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08
Provenance

References & sources

11 references

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

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