Slc25A46b - Solute carrier family 25 member 46b
Predicted to be involved in mitochondrial fission. Located in mitochondrial membrane and plasma membrane. Is expressed in adult head. Used to study neuropathy. Human ortholog(s) of this gene implicated in pontocerebellar hypoplasia type 1E. Orthologous to human SLC25A46 (solute carrier family 25 member 46). [provided by Alliance of Genome Resources, Dec 2024]
NCBI Orthologs
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Protein alignment
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Species | Gene | Architecture | aa |
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