Slc7a14 - solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 Gene

Mus musculus

Also known as A930013N06

Gene ID: 241919 | Gene type: protein coding

About Slc7a14

Summary

Predicted to enable amino acid transmembrane transporter activity. Predicted to be involved in amino acid transport. Predicted to be located in cytosol and nucleoplasm. Predicted to be active in plasma membrane. Is expressed in several structures, including central nervous system; eye; and pancreas trunk epithelium. Human ortholog(s) of this gene implicated in retinitis pigmentosa 68. Orthologous to human SLC7A14 (solute carrier family 7 member 14). [provided by Alliance of Genome Resources, Apr 2022]

Slc7a14 Products(1)

mRNA	Protein	Name
NM_172861.3	NP_766449.1	probable cationic amino acid transporter

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	Reference	Source
enables gamma-aminobutyric acid transmembrane transporter activity	IDA IDA: Inferred from direct assay	36640347	MGI

Biological Process GO Annotation	Evidence	Reference	Source
involved in gamma-aminobutyric acid import	IMP IMP: Inferred from mutant phenotype	36640347	MGI

Cellular Component GO Annotation	Evidence	Reference	Source
located in lysosomal membrane	IDA IDA: Inferred from direct assay	36640347	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

probable cationic amino acid transporter

solute carrier family 7, member 14

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13327	SLC7A14 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Slc7a14	NCBI	NCBI:57709

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