atp8a2 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (65)

Interactants (0)

XB-GENEPAGE-6036031

Gene Symbol: atp8a2 Gene Name: ATPase, aminophospholipid transporter, class I, type 8A, member 2

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (15 sources): Abnormality of movement, Abnormality of the orbital region, Abnormality of vision, Ataxia, Cataract, Cerebral palsy, Cleft palate, Gait disturbance, Hyperreflexia, Hypotonia, Intellectual disability, Seizure, Short stature, Skeletal muscle atrophy, Strabismus [+]
Mouse (37 sources): abnormal cone electrophysiology, abnormal enterocyte morphology, abnormal enzyme/coenzyme level, abnormal retina cone cell outer segment morphology, abnormal retina pigment epithelium morphology, abnormal rod electrophysiology, abnormal spinal cord white matter morphology, abnormal startle reflex, abnormal voluntary movement, axonal dystrophy, behavior/neurological phenotype, brain vacuoles, chromatolysis, cochlear ganglion degeneration, decreased body size, decreased retina photoreceptor cell number, decreased startle reflex, disheveled coat, disorganized photoreceptor outer segment, hearing/vestibular/ear phenotype, hunched posture, impaired limb coordination, increased or absent threshold for auditory brainstem response, lethality at weaning, complete penetrance, lethality at weaning, incomplete penetrance, limb grasping, nervous system phenotype, optic nerve degeneration, pancreas necrosis, postnatal lethality, postnatal lethality, complete penetrance, premature death, preweaning lethality, complete penetrance, retina photoreceptor degeneration, short photoreceptor outer segment, thin retina outer nuclear layer, vision/eye phenotype [+]
View all ortholog results at Monarch