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Symbol Name ID |
Med12
mediator complex subunit 12 MGI:1926212 |
| Darker colors indicate more annotations |
| Human Phenotypes | Prominent occiput |
Craniosynostosis |
Plagiocephaly |
Micrognathia |
Malar flattening |
Macrocephaly |
Widely patent fontanelles and sutures |
Clinodactyly of the 2nd finger |
Abnormal thumb morphology |
Broad toe |
Finger syndactyly |
Limited elbow extension and supination |
Sacral dimple |
Progressive flexion contractures |
Generalized joint hypermobility |
Abnormal sternum morphology |
| Disease(s) Associated with MED12 | ||||||||||||||||
| FG syndrome |
| Mouse Phenotypes | abnormal neurocranium morphology |
abnormal vertebral spinous process morphology |
absent vertebral arch |
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| Availability | Mouse Genotype | |||
| Med12tm1.1Hsch/Med12+ Tg(CMV-cre)1Cgn/0 (conditional) |
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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 07/02/2024 MGI 6.13 |
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