cilk1 Phenotypes

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Phenotypes

Gene Literature (10)

Nucleotides (49)

Interactants (19)

XB-GENEPAGE-985840

Gene Symbol: cilk1 Gene Name: ciliogenesis associated kinase 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (50 sources): Abnormal cerebellum morphology, Abnormal pinna morphology, Abnormality of eye movement, Abnormality of the mouth, Adrenal hypoplasia, Aggressive behavior, Ambiguous genitalia, Aplasia/Hypoplasia of the corpus callosum, Barrel-shaped chest, Bilateral tonic-clonic seizure, Brachydactyly, Cleft palate, Cleft upper lip, Cryptorchidism, Depressed nasal tip, EEG with generalized polyspikes, EEG with polyspike wave complexes, Enlarged kidney, Febrile seizure (within the age range of 3 months to 6 years), Generalized non-motor (absence) seizure, Generalized-onset seizure, Holoprosencephaly, Hydrocephalus, Hyperechogenic kidneys, Hypospadias, Low-set ears, Malar flattening, Micrognathia, Micromelia, Micropenis, Microphallus, Midface retrusion, Morning myoclonic jerks, Narrow chest, Natal tooth, Photosensitive tonic-clonic seizure, Polydactyly, Postaxial polydactyly, Preaxial polydactyly, Sandal gap, Sex reversal, Shield chest, Small scrotum, Status epilepticus, Syndactyly, Ulnar deviation of the hand, Ulnar deviation of the hand or of fingers of the hand, Ventriculomegaly, Wide intermamillary distance, Wide nasal bridge [+]
Mouse (8 sources): abnormal bone mineralization, abnormal digit development, abnormal kidney development, abnormal primary cilium morphology, abnormal skeleton development, delayed bone ossification, lethality throughout fetal growth and development, complete penetrance, nervous system phenotype
View all ortholog results at Monarch