kif14l Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (90)

Interactants (7)

XB-GENEPAGE-5889658

Gene Symbol: kif14l Gene Name: kinesin family member 14 like

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (44 sources): Abnormal cortical bone morphology, Agenesis of corpus callosum, Anteverted nares, Arthrogryposis multiplex congenita, Attention deficit hyperactivity disorder, Bifid uvula, Blindness, Cerebellar hypoplasia, Cerebral hypoplasia, Delayed gross motor development, Generalized hypotonia, Global developmental delay, Gray matter heterotopia, Growth delay, Hyperechogenic kidneys, Hyperreflexia, Hypoplasia of the frontal lobes, Intellectual disability, Intellectual disability, severe, Intrauterine growth retardation, Low-set ears, Microcephaly, Micrognathia, Microphthalmia, Oligohydramnios, Optic nerve hypoplasia, Pachygyria, Poor speech, Renal agenesis, Renal hypoplasia, Rocker bottom foot, Short stature, Simplified gyral pattern, Sloping forehead, Small cerebral cortex, Strabismus, Thin upper lip vermilion, Unilateral renal agenesis, Upslanted palpebral fissure, Ureteral hypoplasia, Vaginal atresia, Ventriculomegaly, Vesicoureteral reflux, Wide nasal bridge [+]
Mouse (22 sources): abnormal Purkinje cell dendrite morphology, abnormal cerebellar cortex morphology, abnormal cerebellar granule cell migration, abnormal cerebral cortex morphology, abnormal locomotor coordination, abnormal motor capabilities/coordination/movement, abnormal oligodendrocyte physiology, behavior/neurological phenotype, decreased body size, decreased brain size, decreased brain weight, decreased cell proliferation, ectopic Purkinje cell, ectopic cerebral cortex pyramidal cells, impaired balance, increased apoptosis, nervous system phenotype, postnatal lethality, complete penetrance, slow postnatal weight gain, small olfactory bulb, thin cerebral cortex, weakness [+]
View all ortholog results at Monarch