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Symbol Name ID |
Cdk5rap2
CDK5 regulatory subunit associated protein 2 MGI:2384875 |
| Darker colors indicate more annotations |
| Human Phenotypes | Craniosynostosis |
Micrognathia |
Microcephaly |
Primary microcephaly |
Abnormal dental enamel morphology |
Clinodactyly of the 5th finger |
Sandal gap |
Joint hypermobility |
Delayed skeletal maturation |
Cone-shaped epiphysis |
Hip dysplasia |
Scoliosis |
| Disease(s) Associated with CDK5RAP2 | ||||||||||||
| primary autosomal recessive microcephaly 3 | ||||||||||||
| Seckel syndrome |
| Mouse Phenotypes | abnormal cranium morphology |
kyphosis |
decreased bone mineral content |
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| Availability | Mouse Genotype | |||
| Cdk5rap2an/Cdk5rap2an | ||||
| Cdk5rap2tm1a(EUCOMM)Wtsi/Cdk5rap2tm1a(EUCOMM)Wtsi | ||||
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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