Gene-Disorder Association · Article
Gene
MYC MYC Proto-Oncogene, BHLH Transcription Factor
×
First reported
1950
Supporting publications
1
Manually curated Approved treatment annotated
Association Review
In brief The association between MYC (MYC Proto-Oncogene, BHLH Transcription Factor) and Leukemia, Acute Lymphoblastic is reported, with clinical genetic testing available, supported by 2 contributing sources.
Sources
2
Clinical variants
0
Symptoms
5
Compounds
2
Trials
90 of 599 via MYC compounds
Publications
1
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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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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A gene summary alongside the source descriptions it was distilled from.
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Leukemia, Acute Lymphoblastic
The disorder 21 database identifiers
The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).
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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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Genomic context
Regulatory context 2 regulatory elements
GeneHancer regulatory elements for the pair, with coordinates, score, element type and supporting literature.
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Interventions
Therapeutics 2 compounds & drugs
Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.
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Human studies
Clinical trials 599 clinical trials
Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.
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Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.
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Provenance
References & sources 9 references
Every source and publication cited across this dossier, as one numbered reference list.
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