slc25a42 solute carrier family 25 member 42
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: slc25a42 assayed (8 sources)|
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
|Human (15 sources): Ataxia, Choreoathetosis, Delayed ability to walk, Delayed speech and language development, Developmental regression, Dystonia, Elevated serum creatine kinase, Generalized hypotonia, Global developmental delay, Hyperammonemia, [+]|
|Mouse (1 source): preweaning lethality, incomplete penetrance|
View all ortholog results at Monarch