Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (23) GO Terms (78) Nucleotides (117) Proteins (52) Interactants (57) Wiki
XB-GENEPAGE-484312

slc9a1     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, [+]
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, [+]

View all ortholog results at Monarch