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Symbol
Name
ID

Med12
mediator complex subunit 12
MGI:1926212

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes

Prominent occiput

Craniosynostosis

Plagiocephaly

Micrognathia

Malar flattening

Macrocephaly

Widely patent fontanelles and sutures

Short chin

High forehead

Long philtrum

Thick vermilion border

High palate

Open mouth

Wide mouth

Fused teeth

Dental crowding

Drooling

Choanal atresia

Prominent nose

Downslanted palpebral fissures

Disease(s) Associated with MED12

FG syndrome

Mouse Phenotypes		abnormal neurocranium morphology	abnormal pharyngeal arch morphology	abnormal first pharyngeal arch morphology	absent second pharyngeal arch	absent third pharyngeal arch
Availability	Mouse Genotype	abnormal neurocranium morphology	abnormal pharyngeal arch morphology	abnormal first pharyngeal arch morphology	absent second pharyngeal arch	absent third pharyngeal arch
	Med12^tm1Hsch/Y
	Med12^tm1.1Hsch/Med12⁺ Tg(CMV-cre)1Cgn/0 (conditional)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 07/02/2024 MGI 6.13