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 |
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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) |
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last database update 09/03/2024 MGI 6.24 |
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