Genopathy
Gene-Disorder Association · Article
Gene
PRKCSH
PRKCSH Beta Subunit Of Glucosidase II
Disorder
Polycystic Liver Disease 1 With Or Without Kidney Cysts
First reported 2000
Supporting publications 15
Key publication · gene–disorder Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13.2-13.1.American journal of human genetics · 2000
Key publication · disorder Jaundice associated with polycystic liver disease. Relief by surgical decompression of the cysts.Archives of surgery (Chicago, Ill. : 1960) · 1976
Manually curated
Association Review

In brief

The association between PRKCSH (PRKCSH Beta Subunit Of Glucosidase II) and Polycystic Liver Disease 1 With Or Without Kidney Cysts is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 2
Clinical variants 188
Symptoms 28
Compounds 0
Trials 0
Publications 15
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

2 sources

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

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03
PRKCSH

The gene

1 source summary

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

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04
Polycystic Liver Disease 1 With Or Without Kidney Cysts

The disorder

9 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

9 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

188 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

15 publications

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

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09
Provenance

References & sources

13 references

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

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