Genopathy
Gene-Disorder Association · Article
Gene
RUNX1
RUNX Family Transcription Factor 1
Manually curatedApproved treatment annotated
Association Review

In brief

The association between RUNX1 (RUNX Family Transcription Factor 1) and Myelodysplastic Syndrome is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 1
Compounds 1
Trials 4of 516 via RUNX1 compounds
Publications 32
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
RUNX1

The gene

2 source summaries

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

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04
Myelodysplastic Syndrome

The disorder

11 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
Mechanism overlap

Shared mechanisms

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

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07
Interventions

Therapeutics

1 compound or drug

Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.

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08
Human studies

Clinical trials

516 clinical trials

Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.

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09
Literature

Reading

32 publications

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

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10
Provenance

References & sources

14 references

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

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