Gene-Disorder Association · Article
Gene
GATA2 GATA Binding Protein 2
×
First reported
2011
Supporting publications
6
Manually curated Approved treatment annotated
Association Review
In brief The association between GATA2 (GATA Binding Protein 2) and Leukemia, Acute Myeloid is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis, pathogenic variants, and a susceptibility locus.
Sources
3
Clinical variants
98
Symptoms
5
Compounds
2
Trials
379 of 799 via GATA2 compounds
Publications
6
Contents
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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2 source summaries
A gene summary alongside the source descriptions it was distilled from.
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04
Leukemia, Acute Myeloid
The disorder 27 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
ClinVar and variant evidence
Genetic basis 98 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
Interventions
Therapeutics 2 compounds & drugs
Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.
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09
Human studies
Clinical trials 799 clinical trials
Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.
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6 publications
Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.
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11
Provenance
References & sources 15 references
Every source and publication cited across this dossier, as one numbered reference list.
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