SLC25A22 - Slc25a22 solute carrier family 25 member 22 Gene

Also Known as GC1; GC-1; RGD1307826

Species: Rattus norvegicus

Gene Type: protein coding
Gene ID: 309111

Summary

Predicted to enable L-glutamate transmembrane transporter activity. Predicted to be involved in L-glutamate transmembrane transport. Predicted to be located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 3. Orthologous to human SLC25A22 (solute carrier family 25 member 22). [provided by Alliance of Genome Resources, Apr 2022]

SLC25A22 Products (1)

mRNA Protein Name
NM_001014027.1 NP_001014049.1 mitochondrial glutamate carrier 1

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables L-glutamate transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
19584051 RGD
Biological Process GO Annotation Evidence References Source
involved in L-glutamate transmembrane transport IMP
IMP: Inferred from mutant phenotype
19584051 RGD
involved in regulation of insulin secretion IMP
IMP: Inferred from mutant phenotype
19584051 RGD
Cellular Component GO Annotation Evidence References Source
located in mitochondrial inner membrane IDA
IDA: Inferred from direct assay
19584051 RGD
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

mitochondrial glutamate carrier 1

  • glutamate/H(+) symporter 1

  • mitochondrial glutamate carrier 1-like

  • solute carrier family 25 (mitochondrial carrier, glutamate), member 22

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13103 SLC25A22 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens SLC25A22 NCBI NCBI:79751