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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 craniofacial morphology |
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 frontonasal prominence morphology |
small frontonasal prominence |
abnormal palatal mesenchymal cell proliferation |
abnormal secondary palate development |
failure of palatal shelf elevation |
palatal shelves fail to meet at midline |
palatal shelf hypoplasia |
abnormal first pharyngeal arch morphology |
absent second pharyngeal arch |
second pharyngeal arch hypoplasia |
cleft palate |
abnormal tongue morphology |
glossoptosis |
abnormal nasal cartilage morphology |
nasal cartilage hypoplasia |
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| Availability | Mouse Genotype | ||||||||||||||||||||||||||||||||
| Med23snouty/Med23snouty | |||||||||||||||||||||||||||||||||
| Med23tm1c(KOMP)Wtsi/Med23tm1c(KOMP)Wtsi H2az2Tg(Wnt1-cre)11Rth/H2az2+ (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 04/16/2024 MGI 6.23 |
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