Gene-Disorder Association · Article
Gene
ERCC2 ERCC Excision Repair 2, TFIIH Core Complex Helicase Subunit
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First reported
2004
Supporting publications
6
Manually curated Approved treatment annotated
Association Review
In brief The association between ERCC2 (ERCC Excision Repair 2, TFIIH Core Complex Helicase Subunit) and Melanoma is reported, with clinical genetic testing available.
Sources
1
Clinical variants
0
Symptoms
2
Compounds
3
Trials
104 of 5,139 via ERCC2 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 1 source
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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7 database identifiers
The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).
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05
Interventions
Therapeutics 3 compounds & drugs
Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.
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06
Human studies
Clinical trials 5,139 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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08
Provenance
References & sources 12 references
Every source and publication cited across this dossier, as one numbered reference list.
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