Slc25a22 - solute carrier family 25 (mitochondrial carrier, glutamate), member 22 Gene

Also Known as Gc1; 1300006L01Rik

Species: Mus musculus

Gene Type: protein coding
Gene ID: 68267

Summary

Predicted to enable L-aspartate transmembrane transporter activity and L-glutamate transmembrane transporter activity. Predicted to be involved in L-glutamate transmembrane transport; aspartate transmembrane transport; and malate-aspartate shuttle. Located in mitochondrion. Is expressed in alimentary system; eye; liver; and nervous system. 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 (4)

mRNA Protein Name
NM_001177576.1 NP_001171047.1 mitochondrial glutamate carrier 1 isoform a
NM_001360723.1 NP_001347652.1 mitochondrial glutamate carrier 1 isoform a
NM_001360724.1 NP_001347653.1 mitochondrial glutamate carrier 1 isoform b
NM_026646.3 NP_080922.1 mitochondrial glutamate carrier 1 isoform a
Protein Preferred Names Protein Names

mitochondrial glutamate carrier 1

  • glutamate/H(+) symporter 1

  • solute carrier family 25 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