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SLC25A46 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008].. Additionally we are shipping SLC25A46 Antibodies (20) and SLC25A46 Proteins (3) and many more products for this protein.
recently, the "Turning calves syndrome", a novel sensorimotor polyneuropathy was described in the French Rouge-des-Pres cattle breed. In the present study, we determined that this hereditary disease resulted from a single nucleotide substitution in SLC25A46, a gene encoding a protein of the mitochondrial carrier family. This mutation caused an apparent damaging amino-acid substitution.
we showed that the Slc25a46 disruption caused a fusion/fission imbalance and an abnormal mitochondrial architecture that disturbed mitochondrial metabolism. These data extended the range of phenotypes associated with Slc25a46 dysfunction. Moreover, this Slc25a46 knock-out mouse model should be useful to further elucidate the role of SLC25A46 in mitochondrial dynamics
Our mutant mice provide a valid model for understanding the mechanistic basis of the complex SLC25A46-mediated pathologies, as well as for screening potential therapeutic interventions.
Data indicate four families with recessive mutations in solute carrier family 25 member 46 protein (SLC25A46).
Compares and contrasts all the known human SLC25A (show SLC25A25 ELISA Kits)* genes and includes functional information.
SLC25A46 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006
solute carrier family 25, member 46
, solute carrier family 25 member 46-like
, solute carrier family 25 member 46
, solute carrier family 25 member 46-B