cep152 Phenotypes

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Phenotypes

Gene Literature (14)

Nucleotides (165)

Interactants (360)

XB-GENEPAGE-988608

Gene Symbol: cep152 Gene Name: centrosomal protein 152kDa

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (59 sources): 11 pairs of ribs, Abnormal cortical bone morphology, Abnormal cortical gyration, Abnormal dental enamel morphology, Abnormal earlobe morphology, Absent earlobe, Agenesis of corpus callosum, Aggressive behavior, Bimanual synkinesia, Blepharophimosis, Cachexia, Clinodactyly of the 5th finger, Clitoral hypertrophy, Cognitive impairment, Cone-shaped epiphysis, Convex nasal ridge, Craniosynostosis, Cryptorchidism, Delayed skeletal maturation, Downslanted palpebral fissures, Glaucoma, Global developmental delay, Gray matter heterotopia, Growth delay, High palate, Hip dysplasia, Hyperreflexia, Hypodontia, Hypoplasia of the frontal lobes, Impulsivity, Intellectual disability, Intellectual disability, severe, Intrauterine growth retardation, Large beaked nose, Microcephaly, Micrognathia, Mild global developmental delay, Narrow face, Oligodontia, Pachygyria, Pes planus, Prematurely aged appearance, Prominent nasal bridge, Retrognathia, Sandal gap, Scoliosis, Selective tooth agenesis, Short stature, Simplified gyral pattern, Sloping forehead, Sparse scalp hair, Strabismus, Thin upper lip vermilion, Tooth agenesis, Unilateral renal agenesis, Upslanted palpebral fissure, Ventriculomegaly, Vesicoureteral reflux, obsolete Joint hyperflexibility [+]
Mouse (4 sources): abnormal centrosome morphology, abnormal embryonic neuroepithelium morphology, decreased embryonic neuroepithelium primary cilium number, increased apoptosis
View all ortholog results at Monarch