slc9a1 Phenotypes

Phenotypes

XB-GENEPAGE-484312

Gene Symbol: slc9a1 Gene Name: solute carrier family 9 member 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (11 sources): Action tremor, Ataxia, Cerebellar atrophy, Dysarthria, Dysdiadochokinesis, Dysmetria, Gait ataxia, Limb ataxia, Motor delay, Nystagmus, Short stature [+]
Mouse (33 sources): abnormal axon morphology, abnormal cerebellar molecular layer, abnormal cerebellum deep nucleus morphology, abnormal cerebellum dentate nucleus morphology, abnormal epidermis stratum corneum morphology, abnormal fertility/fecundity, abnormal locomotor coordination, abnormal parotid gland physiology, abnormal PR interval, abnormal Purkinje cell morphology, abnormal stomach glandular epithelium morphology, abnormal synaptic bouton morphology, abnormal vestibular ganglion morphology, behavioral arrest, cochlear ganglion degeneration, convulsive seizures, decreased body size, decreased exploration in new environment, decreased heart weight, decreased response of heart to induced stress, decreased salivation, endocrine/exocrine gland phenotype, growth/size/body region phenotype, homeostasis/metabolism phenotype, lethality at weaning, incomplete penetrance, nervous system phenotype, neuron degeneration, poor grooming, postnatal lethality, postnatal lethality, incomplete penetrance, premature death, preweaning lethality, incomplete penetrance, Purkinje cell degeneration [+]
View all ortholog results at Monarch