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Editorially curated · om-repository-of-mutations
Repository of Mutations from Oman
Systematically compiled genetic disorders and mutations reported in Oman to support diagnosis, research prioritization and national database development.
01 / Project overview
What the record establishes.
- Geographic scope
- Omani patients and families represented in published literature
- Project type
- Variant and disease database
- Research domain
- Inherited disease and clinical variant curation
- Years
- Not stated
- Lifecycle status
- completed
- Status basis
- The 2015 peer-reviewed article presents ROM as an entry point to a national mutation database; no current maintained public endpoint was identified.
- Status evidence date
- 2015-11-18
- Scale
- Publication-defined mutation repository; current record total was not independently verified.
02 / Organizations and population
Who and what the project connects.
- Lead organizations
- Omani clinical genetics researchers
- Partner organizations
- Not stated
- Organism / population
- Omani individuals with reported inherited disorders
03 / Data and access
What exists and how it can be reached.
Data types
- variant curation
- disease-gene associations
- bibliographic data
Data access
Publication-accessible; live database not found
Identifiers
- PMCID
PMCID:PMC4648203
04 / Evidence and provenance
Why the record is included.
Inclusion basis
Named national variant-resource project with a primary publication.
Editorial note
Classify the historical compilation as completed; do not imply that a maintained online database currently exists.
Sources
- primary record source Verified 2026-08-15
Release v0.2.0