Genopathy
Gene-Disorder Association · Article
Gene
KLK1
Kallikrein 1
Disorder
Kallikrein, Decreased Urinary Activity Of
First reported 2002
Key publication · disorder Loss-of-function polymorphism of the human kallikrein gene with reduced urinary kallikrein activity.Journal of the American Society of Nephrology : JASN · 2002
Manually curated
Association Review

In brief

The association between KLK1 (Kallikrein 1) and Kallikrein, Decreased Urinary Activity Of is a manually-curated gene–disease association, with its 2 contributing sources — 1 of them expert-curated — recording a known molecular basis.

Sources 2
Clinical variants 1
Symptoms 0
Compounds 0
Trials 0
Publications 0
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
KLK1

The gene

1 source summary

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

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04
Kallikrein, Decreased Urinary Activity Of

The disorder

2 database identifiers

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

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05
ClinVar and variant evidence

Genetic basis

1 clinical variant

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

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06
Provenance

References & sources

4 references

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

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