Genopathy
Gene-Disorder Association · Article
Gene
SETBP1
SET Binding Protein 1
Disorder
Juvenile Myelomonocytic Leukemia
First reported 1969
Key publication · disorder [Clinico-hematological considerations on a case of juvenile chronic myeloid leukemia].Minerva pediatrica · 1969
Manually curated
Association Review

In brief

The association between SETBP1 (SET Binding Protein 1) and Juvenile Myelomonocytic Leukemia is a manually-curated gene–disease association, drawing on a single expert-curated source, which records causative variation.

Sources 1
Clinical variants 0
Symptoms 4
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

1 source

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

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03
SETBP1

The gene

1 source summary

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

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04
Juvenile Myelomonocytic Leukemia

The disorder

12 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

1 clinical feature

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

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06
Provenance

References & sources

5 references

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

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