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Summary Expression Phenotypes Gene Literature (8) GO Terms (2) Nucleotides (100) Proteins (51) Interactants (214) Wiki
XB-GENEPAGE-940057

slc18a2     solute carrier family 18 member A2

Expression Phenotypes
Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: slc18a2 assayed (5 sources)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (31 sources): Abnormal foot morphology, Abnormality of coordination, Abnormality of eye movement, Abnormality of the vasculature, Ataxia, Axial hypotonia, Cognitive impairment, Dysarthria, Dysdiadochokinesis, Dystonia, [+]
Mouse (48 sources): abnormal associative learning, abnormal circadian behavior, abnormal corticosterone level, abnormal dopamine level, abnormal dopaminergic neuron morphology, abnormal liquid preference, abnormal motor capabilities/coordination/movement, abnormal neurotransmitter secretion, abnormal neurotransmitter uptake, abnormal noradrenaline level, [+]

View all ortholog results at Monarch