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Craniosynostosis v2.0 MED12 Gene migrated from ENSG00000184634 to ENSG00000184634 (gene set migration)
Craniosynostosis v1.88 MED12 Zornitza Stark Marked gene: MED12 as ready
Craniosynostosis v1.88 MED12 Zornitza Stark Gene: med12 has been classified as Amber List (Moderate Evidence).
Craniosynostosis v1.88 MED12 Zornitza Stark Classified gene: MED12 as Amber List (moderate evidence)
Craniosynostosis v1.88 MED12 Zornitza Stark Gene: med12 has been classified as Amber List (Moderate Evidence).
Craniosynostosis v1.87 MED12 Zornitza Stark gene: MED12 was added
gene: MED12 was added to Craniosynostosis. Sources: Literature
Mode of inheritance for gene: MED12 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Publications for gene: MED12 were set to 19938245
Phenotypes for gene: MED12 were set to Opitz-Kaveggia (FG) syndrome, MIM#305450
Review for gene: MED12 was set to AMBER
Added comment: Craniosynostosis is a rare feature of this syndrome.
Sources: Literature