Slc25a12 - solute carrier family 25 member 12 Gene
Also Known as Aralar1; RGD1561141
Species: Rattus norvegicus
Summary
Predicted to enable acidic amino acid transmembrane transporter activity; calcium ion binding activity; and identical protein binding activity. Involved in several processes, including malate-aspartate shuttle; positive regulation of ATP biosynthetic process; and regulation of glucose metabolic process. Predicted to be located in mitochondrion. Human ortholog(s) of this gene implicated in Asperger syndrome; autistic disorder; and developmental and epileptic encephalopathy 39. Orthologous to human SLC25A12 (solute carrier family 25 member 12). [provided by Alliance of Genome Resources, Apr 2022]
Slc25a12 Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001399269.1 | NP_001386198.1 | electrogenic aspartate/glutamate antiporter SLC25A12, mitochondrial |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in glutamate biosynthetic process |
IMP
IMP: Inferred from mutant phenotype
|
19764902 | RGD |
| involved in malate-aspartate shuttle |
IMP
IMP: Inferred from mutant phenotype
|
19764902 | RGD |
| involved in negative regulation of glucose catabolic process to lactate via pyruvate |
IMP
IMP: Inferred from mutant phenotype
|
19764902 | RGD |
| involved in positive regulation of ATP biosynthetic process |
IMP
IMP: Inferred from mutant phenotype
|
19764902 | RGD |
| involved in positive regulation of glucose metabolic process |
IMP
IMP: Inferred from mutant phenotype
|
19764902 | RGD |
| involved in positive regulation of myelination |
IMP
IMP: Inferred from mutant phenotype
|
20015484 | RGD |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
electrogenic aspartate/glutamate antiporter SLC25A12, mitochondrial calcium-binding mitochondrial carrier protein Aralar1 |
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