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Symbol
Name
ID

Med23
mediator complex subunit 23
MGI:1917458

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Spasticity	Hypoplasia of the pons	Thin corpus callosum	Choreoathetosis	Expressive language delay	Irritability	Intellectual disability	Intellectual disability, profound	Sleep abnormality	Dystonia
Disease(s) Associated with MED23
autosomal recessive intellectual developmental disorder 18

Mouse Phenotypes		nervous system phenotype	impaired cranial neural crest cell differentiation	abnormal nervous system development	abnormal trigeminal ganglion morphology
Availability	Mouse Genotype	nervous system phenotype	impaired cranial neural crest cell differentiation	abnormal nervous system development	abnormal trigeminal ganglion morphology
	Med23^snouty/Med23^snouty
	Med23^tm1Berk/Med23^tm1Berk
	Med23^{tm1c(KOMP)Wtsi}/Med23^{tm1c(KOMP)Wtsi} H2az2^{Tg(Wnt1-cre)11Rth}/H2az2⁺ (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 04/23/2024 MGI 6.23