Symbol Name ID |
Med12
mediator complex subunit 12 MGI:1926212 |
Darker colors indicate more annotations |
Human Phenotypes | Death in infancy |
Disease(s) Associated with MED12 | |
FG syndrome |
Mouse Phenotypes | embryonic lethality during organogenesis, complete penetrance |
embryonic lethality during organogenesis, incomplete penetrance |
embryonic lethality between implantation and somite formation, complete penetrance |
embryonic lethality, complete penetrance |
prenatal lethality, incomplete penetrance |
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Availability | Mouse Genotype | |||||
Med12tm1.2Hsch/Y | ||||||
Med12tm1Hsch/Y | ||||||
Med12tm1.1Hsch/Med12+ Tg(CMV-cre)1Cgn/0 (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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