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

Mus musculus

Also known as Gc1; 1300006L01Rik

Gene ID: 68267 | Gene type: protein coding

About Slc25a22

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

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

Name
Email *

	Sorry, but the email address you supplied was invalid.