Epidermolysis bullosa simplex 2B, generalized intermediate: genes and variants

Epidermolysis bullosa simplex 2B, generalized intermediate is linked to 1 analyzed protein (KRT5). 5 DNA variants are known to cause it; 3 more are uncertain, and 0 of those already look disease-causing on computable evidence.

Last updated 2026-09-30. Research information, not medical advice.

Genes linked to Epidermolysis bullosa simplex 2B, generalized intermediate

Where Epidermolysis bullosa simplex 2B, generalized intermediate variants cluster

Known disease-causing variants in Epidermolysis bullosa simplex 2B, generalized intermediate

VariantPositionProtein partClinical label
KRT5 V323A323IF rodDisease-causing (★★)
KRT5 E477K477IF rodDisease-causing (★★)
KRT5 G476D476IF rodDisease-causing (★★)
KRT5 V323M323IF rodDisease-causing (★)
KRT5 V7A7HeadDisease-causing

Same protein, different disease

Diseases related to Epidermolysis bullosa simplex 2B, generalized intermediate

Frequently asked questions

Which genes are linked to Epidermolysis bullosa simplex 2B, generalized intermediate?

In CATVariant, Epidermolysis bullosa simplex 2B, generalized intermediate is linked to 1 analyzed protein: KRT5 (Keratin, type II cytoskeletal 5).

How many genetic variants are linked to Epidermolysis bullosa simplex 2B, generalized intermediate?

24 variants: 5 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 3 are of uncertain significance or have conflicting reports.

Which uncertain variants in Epidermolysis bullosa simplex 2B, generalized intermediate look disease-causing?

None of the uncertain variants currently reaches the likely-pathogenic range on computable evidence alone.

About this data

Variant–disease links come from ClinVar, Open Targets and UniProt, pooled from the latest public CATVariant analysis of each human protein. Evidence scores use the ACMG/AMP Bayesian points scale with computable criteria only (position among known disease variants, rarity in gnomAD, calibrated predictors, deep mutational scanning); there is no family or patient data, so they prioritise variants for expert review and never classify them.

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