| 1308811 | Slc25a26 | solute carrier family 25 member 26 | ENCODES a protein that exhibits S-adenosyl-L-methionine transmembrane transporter activity (ortholog); S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity (ortholog); INVOLVED IN macromolecule methylation (ortholog); mitochondrial S-adenosyl-L-methionine transmembrane transport (or tholog); S-adenosyl-L-methionine transport (ortholog); ASSOCIATED WITH combined oxidative phosphorylation deficiency 28 (ortholog); genetic disease (ortholog); Hypokalemic Periodic Paralysis, Type 1 (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 2,4-dinitrotoluene; bisphenol A | 4 | 128591223 | 128687854 | Rat | 66 | symbol , PhenoGen | gene, protein-coding, VALIDATED [RefSeq] |
| 1318797 | SLC25A26 | solute carrier family 25 member 26 | This gene is a member of the mitochondrial carrier family which includes nuclear-encoded transporters localized on the inner mitochondrial membranes. Members of the family transport important small molecules across the mitochondrial inner membrane. This protein is involved in the transport of S-aden osylmethionine (SAM) into the mitochondria. Mutations in this gene are associated with combined oxidative phosphorylation deficiency 28. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017] | 3 | 66133610 | 66378927 | Human | 94 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, REVIEWED [RefSeq] |
| 1553057 | Slc25a26 | solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 26 | Predicted to enable S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity. Predicted to be involved in mitochondrial S-adenosyl-L-methionine transmembrane transport. Located in mitochondrion. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 2 8. Orthologous to human SLC25A26 (solute carrier family 25 member 26). [provided by Alliance of Genome Resources, Jul 2025] | 6 | 94477272 | 94581636 | Mouse | 73 | symbol , PhenoGen , description | gene, protein-coding, VALIDATED [RefSeq] |
| 8974136 | Slc25a26 | solute carrier family 25 member 26 | ENCODES a protein that exhibits S-adenosyl-L-methionine transmembrane transporter activity (ortholog); S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity (ortholog); INVOLVED IN macromolecule methylation (ortholog); mitochondrial S-adenosyl-L-methionine transmembrane transport (or tholog); S-adenosyl-L-methionine transport (ortholog); ASSOCIATED WITH combined oxidative phosphorylation deficiency 28 (ortholog); genetic disease (ortholog); Hypokalemic Periodic Paralysis, Type 1 (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog) | NW_004955421 | 21220071 | 21334330 | Chinchilla | 13 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 11847330 | SLC25A26 | solute carrier family 25 member 26 | ENCODES a protein that exhibits S-adenosyl-L-methionine transmembrane transporter activity (inferred); S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity (inferred); INVOLVED IN macromolecule methylation (ortholog); ASSOCIATED WITH combined oxidative phosphorylation deficiency 28 (ortholog); genetic disease (ortholog); Hypokalemic Periodic Paralysis, Type 1 (ortholog); FOUND IN membrane (inferred); mitochondrial inner membrane (inferred); mitochondrion (inferred) | 3 | 66112241 | 66271151 | Bonobo | 18 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 12361470 | SLC25A26 | solute carrier family 25 member 26 | ENCODES a protein that exhibits S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity (ortholog); INVOLVED IN macromolecule methylation (ortholog); mitochondrial S-adenosyl-L-methionine transmembrane transport (ortholog); S-adenosyl-L-methionine transport (ortholog); ASSOCIATED WITH combined oxidative phosphorylation deficiency 28 (ortholog); genetic disease (ortholog); Hypokalemic Periodic Paralysis, Type 1 (ortholog); FOUND IN membrane (inferred); mitochondrial inner membrane (inferred); mitochondrion (inferred) | 20 | 25032708 | 25167574 | Dog | 16 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 12692098 | Slc25a26 | solute carrier family 25 member 26 | ENCODES a protein that exhibits S-adenosyl-L-methionine transmembrane transporter activity (inferred); S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity (inferred); INVOLVED IN macromolecule methylation (ortholog); ASSOCIATED WITH combined oxidative phosphorylation deficiency 28 (ortholog); genetic disease (ortholog); Hypokalemic Periodic Paralysis, Type 1 (ortholog); FOUND IN membrane (inferred); mitochondrial inner membrane (inferred); mitochondrion (inferred) | NW_004936637 | 239416 | 371635 | Squirrel | 16 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 18904740 | Slc25a26 | solute carrier family 25 member 26 | ENCODES a protein that exhibits S-adenosyl-L-methionine transmembrane transporter activity (ortholog); S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity (ortholog); INVOLVED IN macromolecule methylation (ortholog); mitochondrial S-adenosyl-L-methionine transmembrane transport (or tholog); S-adenosyl-L-methionine transport (ortholog); ASSOCIATED WITH combined oxidative phosphorylation deficiency 28 (ortholog); genetic disease (ortholog); Hypokalemic Periodic Paralysis, Type 1 (ortholog); FOUND IN membrane (inferred); mitochondrial inner membrane (inferred); mitochondrion (inferred) | | | | Naked Mole-Rat | 15 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 18599893 | SLC25A26 | solute carrier family 25 member 26 | ENCODES a protein that exhibits S-adenosyl-L-methionine transmembrane transporter activity (inferred); S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity (inferred); INVOLVED IN macromolecule methylation (ortholog); ASSOCIATED WITH combined oxidative phosphorylation deficiency 28 (ortholog); genetic disease (ortholog); Hypokalemic Periodic Paralysis, Type 1 (ortholog); FOUND IN membrane (inferred); mitochondrial inner membrane (inferred); mitochondrion (inferred) | | | | Green Monkey | 17 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 14264736 | SLC25A26 | solute carrier family 25 member 26 | ENCODES a protein that exhibits S-adenosyl-L-methionine transmembrane transporter activity (inferred); S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity (inferred); INVOLVED IN macromolecule methylation (ortholog); ASSOCIATED WITH combined oxidative phosphorylation deficiency 28 (ortholog); genetic disease (ortholog); Hypokalemic Periodic Paralysis, Type 1 (ortholog); FOUND IN membrane (inferred); mitochondrial inner membrane (inferred); mitochondrion (inferred) | | | | Pig | 20 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 155236194 | slc25a26 | | | | | | Tropical Clawed Frog | | symbol | gene, null |
| 625916473 | Slc25a26 | solute carrier family 25 member 26 | ENCODES a protein that exhibits S-adenosyl-L-methionine transmembrane transporter activity (ortholog); S-adenosyl-L-methionine:S-adenosyl-L-homocysteine antiporter activity (ortholog); INVOLVED IN macromolecule methylation (ortholog); mitochondrial S-adenosyl-L-methionine transmembrane transport (or tholog); S-adenosyl-L-methionine transport (ortholog); ASSOCIATED WITH combined oxidative phosphorylation deficiency 28 (ortholog); genetic disease (ortholog); Hypokalemic Periodic Paralysis, Type 1 (ortholog); FOUND IN mitochondrial inner membrane (ortholog); mitochondrion (ortholog) | | | | Black Rat | 13 | symbol | gene, protein-coding, MODEL [RefSeq] |
| 155246355 | slc25a26.L | | | | | | African Clawed Frog | | symbol | gene, null |