1. Gene
  2. Slc25a1 - solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 Gene

Slc25a1 - solute carrier family 25 (mitochondrial carrier, citrate transporter), member 1 Gene

Mus musculus

Also known as Ctp; Dgsj; Slc20a3; 1300019P08Rik; 2610100G11Rik

Gene ID: 13358 | Gene type: protein coding

About Slc25a1

Summary

Predicted to enable citrate secondary active transmembrane transporter activity. Predicted to be involved in mitochondrial citrate transmembrane transport. Located in mitochondrion. Is expressed in several structures, including adipose tissue; alimentary system; clavicle; liver; and nervous system. Human ortholog(s) of this gene implicated in 2-hydroxyglutaric aciduria; combined D-2- and L-2-hydroxyglutaric aciduria; and congenital myasthenic syndrome. Orthologous to human SLC25A1 (solute carrier family 25 member 1). [provided by Alliance of Genome Resources, Apr 2022]

Slc25a1 Products(1)

mRNA Protein Name
NM_153150.2 NP_694790.1 tricarboxylate transport protein, mitochondrial
Gene Ontology
  • Cellular Component
Cellular Component GO Annotation Evidence Reference Source
located in mitochondrion IDA
IDA: Inferred from direct assay
18775783 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

tricarboxylate transport protein, mitochondrial

DiGeorge syndrome gene j

citrate transport protein

solute carrier family 25 member 1

tricarboxylate carrier protein

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc25a1 NCBI NCBI:6576