Genopathy
Gene-Disorder Association · Article
Gene
SERPINB7
Serpin Family B Member 7
Disorder
Palmoplantar Keratoderma, Nagashima Type
First reported 2013
Supporting publications 4
Key publication · gene–disorder Mutations in SERPINB7, encoding a member of the serine protease inhibitor superfamily, cause Nagashima-type palmoplantar keratosis.American journal of human genetics · 2013
Key publication · disorder "Nagashima-type" keratosis as a novel entity in the palmoplantar keratoderma category.Archives of dermatology · 2008
Manually curated
Association Review

In brief

The association between SERPINB7 (Serpin Family B Member 7) and Palmoplantar Keratoderma, Nagashima Type is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.

Sources 4
Clinical variants 8
Symptoms 15
Compounds 0
Trials 0
Publications 4
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

4 sources

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

Request access
03
SERPINB7

The gene

1 source summary

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

Request access
04
Palmoplantar Keratoderma, Nagashima Type

The disorder

11 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Phenotype

Clinical features

8 clinical features

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

Request access
06
ClinVar and variant evidence

Genetic basis

8 clinical variants

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

Request access
07
Mechanism overlap

Shared mechanisms

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

Request access
08
Literature

Reading

4 publications

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

Request access
09
Provenance

References & sources

11 references

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

Request access