Genopathy
Gene-Disorder Association · Article
Gene
JAK2
Janus Kinase 2
Disorder
Erythrocytosis, Familial, 1
First reported 2005
Key publication · gene–disorder A gain-of-function mutation of JAK2 in myeloproliferative disorders.The New England journal of medicine · 2005
Key publication · disorder Benign familial polycythemia in childhood; report of two cases.Pediatrics · 1958
Manually curated
Association Review

In brief

The association between JAK2 (Janus Kinase 2) and Erythrocytosis, Familial, 1 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.

Sources 3
Clinical variants 10
Symptoms 23
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

3 sources

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

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03
JAK2

The gene

3 source summaries

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

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04
Erythrocytosis, Familial, 1

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

13 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

10 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
Provenance

References & sources

8 references

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

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