|
Symbol Name ID |
Med23
mediator complex subunit 23 MGI:1917458 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
| Disease(s) Associated with MED23 | |
| autosomal recessive intellectual developmental disorder 18 |
| Mouse Phenotypes | abnormal cranium morphology |
abnormal Meckel's cartilage morphology |
Meckel's cartilage hypoplasia |
abnormal cranial cartilage development |
frontal bone hypoplasia |
temporal bone hypoplasia |
small lower incisors |
abnormal tooth development |
growth retardation of incisors |
growth retardation of molars |
mandibular condyloid process hypoplasia |
absent mandibular symphysis |
small mandible |
mandible hypoplasia |
micrognathia |
absent palatine bone |
abnormal nasal cartilage morphology |
nasal cartilage hypoplasia |
decreased bone mineral content |
|
| Availability | Mouse Genotype | |||||||||||||||||||
| Med23em1(IMPC)Wtsi/Med23+ | ||||||||||||||||||||
| Med23tm1c(KOMP)Wtsi/Med23tm1c(KOMP)Wtsi H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
||||||||||||||||||||
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 04/30/2024 MGI 6.23 |
|
|
|
||
Analysis Tools