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Summary Expression Phenotypes Gene Literature (18) GO Terms (2) Nucleotides (52) Proteins (35) Interactants (129) Wiki

slc16a2     solute carrier family 16, member 2 (thyroid hormone transporter)

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.
Manual annotations: slc16a2 manipulated (1 source)
Computed annotations: slc16a2 assayed (1 source)
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + slc16a2 CRISPR + L-T3 (5nM) (1 source)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (56 sources): Abnormal conjugate eye movement, Abnormality of movement, Abnormality of the neck, Absent speech, Aphasia, Ataxia, Athetosis, Babinski sign, Bilateral single transverse palmar creases, Biparietal narrowing, [+]
Mouse (11 sources): abnormal enzyme/coenzyme level, abnormal thyroxine level, abnormal triiodothyronine level, decreased circulating fructosamine level, decreased circulating thyroxine level, decreased triiodothyronine level, increased circulating alkaline phosphatase level, increased circulating amylase level, increased thyroid-stimulating hormone level, increased triiodothyronine level, [+]

View all ortholog results at Monarch