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Symbol
Name
ID
Cep152
centrosomal protein 152
MGI:2139083
Phenotype annotations related to nervous system
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
Availability Mouse Genotype
Cep152tm1a(EUCOMM)Wtsi/Cep152tm1a(EUCOMM)Wtsi

Contributing Projects:
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
The Jackson Laboratory