Symbol Name ID |
Cep152
centrosomal protein 152 MGI:2139083 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Abnormal cortical gyration |
Simplified gyral pattern |
Aggressive behavior |
Compulsive behaviors |
Motor tics |
Impulsivity |
Self-injurious behavior |
Intellectual disability |
Bimanual synkinesia |
Seizure |
Disease(s) Associated with CEP152 | |||||||||||
primary autosomal recessive microcephaly 9 | |||||||||||
Seckel syndrome 5 |
Mouse Phenotypes | decreased embryonic neuroepithelium primary cilium number |
abnormal embryonic neuroepithelium morphology |
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Availability | Mouse Genotype | ||
Cep152tm1a(EUCOMM)Wtsi/Cep152tm1a(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 04/30/2024 MGI 6.23 |
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